Effect of microencapsulatednext term phase change material in sandwich panels
内皮祖细胞膜微粒与脑卒中治疗相关性研究进展
内皮祖细胞膜微粒与脑卒中治疗相关性研究进展邱文姬;陈煜森【摘要】Vascular endothelial dysfunction is related to the occurrence and development of stroke.Endothelial progenitor cells-derived microvesicles (EPC-MVs) can slow the progression of stroke and improve the prognosis of stroke by repairing the damaged vascular endothelium,providing a new method for the treatment of stroke.This article reviews the correlation between EPC-MVs and stroke treatment.%血管内皮功能障碍与脑卒中的发生发展互为因果.内皮祖细胞膜微粒可以通过修复损伤的血管内皮来延缓脑卒中的进展和改善脑卒中患者的预后,为脑卒中的治疗提供了新的方法.本文就内皮祖细胞膜微粒与脑卒中治疗相关性进行综述.【期刊名称】《海南医学》【年(卷),期】2018(029)005【总页数】4页(P674-677)【关键词】内皮祖细胞;内皮祖细胞膜微粒;脑卒中;修复;治疗【作者】邱文姬;陈煜森【作者单位】广东医科大学,广东湛江524000;广东医科大学附属医院,广东湛江524000【正文语种】中文【中图分类】R743.3脑卒中俗称“中风”,是以高发生率、高致残率、高致死率和高复发率为特点的急性脑血管循环障碍性疾病。
一般分为缺血性卒中(如脑梗死)和出血性卒中(如脑出血)两大类。
由于脑供血动脉闭塞,使该动脉的供血区得不到血液中的氧气和营养而发生坏死,被称为缺血性脑卒中,约占80%~85%;而由于脑动脉硬化而血管破裂,血液进入脑内和脑周围间隙,使脑细胞得不到正常血管内运输的氧气和营养供应而发生坏死,另被称为出血性脑卒中,占15%~20%。
到9月9日
到9月9日,社保基金正式进入股市整整3个月,按照有关规定,社保基金必须通过基金管理公司在三个月内完成建仓,并且其持仓市值要达到投资组合总市值80%的水平。
与此前大受追捧的QFII概念相比,社保基金及其所持有的股票显然低调得多,但是在西南证券分析师田磊看来,至少就目前来看,社保基金无论是在资金规模,还是在持股数量上明显都强于境外投资者,其投资理念和行为更可能给市场带来影响。
基金操作的社保基金的选股思路并不侧重某个行业,而更看重企业本身的发展和成长性,并且现阶段的企业经营业绩和走势也不是基金重点考虑的方面。
目前入市的社保基金都是委托南方、博时、华夏、鹏华、长盛、嘉实6家基金管理公司管理。
社保基金大致是被分为14个组合由以上6家管理公司分别管理,每个组合都有一个三位数的代码,第一位代表投资方向,其中“1”指股票投资、“2”指债券投资;第三位数字则代表基金公司名称,其中“1”为南方、“2”为博时、“3”为华夏、“4”为鹏华、“5”为长盛、“6”为嘉实;另有107、108组合主要运作社保基金此前一直持有的中石化股票,分别由博时与华夏基金公司管理。
在许多社保基金介入的股票中经常可以看到开放式基金的身影,例如在被社保基金大量持有的安阳钢铁(600569)的前10大股东中,其第2、6、7、8、9大股东均为开放式基金,而社保基金则以持股500多万股位列第3大股东。
类似的情况也出现在社保基金103组合所持有的华菱管线(000932)上,其第二大股东即为鹏华行业成长证券投资基金,社保基金则以200多万股的持仓量位列第7大股东,此外,在其前10大股东中还有5家是封闭式基金。
对此,某基金公司人士解释说,在获得社保基金管理人资格后,6家基金公司成立了专门的机构理财部门负责社保基金的投资管理,但是其研究、交易系统等则与公募基金共用一个平台,因此社保基金和开放式基金在选股时才会如此一致。
针对“社保概念股”的走势,国盛证券的分析师王剑认为,虽然社保基金此次委托入市资金超过百亿元,但大部分投向是债券,而且由于社保基金的特殊地位,因此基金管理公司对社保基金的操纵策略应该是以“集中持股,稳定股价”为主,不大可能博取太高的收益。
银耳多糖对力竭运动小鼠氧化性损伤所致疲劳的缓解作用
黄小兰,黄少波,邵丽. 银耳多糖对力竭运动小鼠氧化性损伤所致疲劳的缓解作用[J]. 食品工业科技,2024,45(4):328−335. doi:10.13386/j.issn1002-0306.2023040074HUANG Xiaolan, HUANG Shaobo, SHAO Li. Effect of Tremella fuciformis Polysaccharides on Fatigue Induced by Oxidative Damage in Exhaustive Exercise Mice[J]. Science and Technology of Food Industry, 2024, 45(4): 328−335. (in Chinese with English abstract).doi: 10.13386/j.issn1002-0306.2023040074· 营养与保健 ·银耳多糖对力竭运动小鼠氧化性损伤所致疲劳的缓解作用黄小兰1,黄少波2,邵 丽3,*(1.重庆对外经贸学院,重庆 401520;2.重庆市开州区中医院骨伤科,重庆 405400;3.重庆市开州区中医院儿科,重庆 405400)摘 要:目的:探讨银耳多糖(Tremella fuciformis polysaccharides ,TFP )对小鼠力竭运动性氧化损伤的影响,并分析其机制。
方法:采用TFP 处理L6细胞48 h ,CCK-8法检测L6的活力;L6细胞设置3组,包括对照组、H 2O 2组、H 2O 2+TFP 组,孵育48 h ,生化分析仪检测乳酸(Lactic Acid ,LA )水平,Western blot 实验检测Nrf2、NQO1和HO-1蛋白水平;将C57BL/6小鼠随机分为4组(每组n=10),包括模型组、模型+TFP 组(50、100、200 mg/kg ),模型+TFP 组连续灌胃TFP ,模型组灌胃相同剂量的蒸馏水,每天1次,连续2周。
英汉对照 journal of food engering
3D CFD simulation of bottle emptying processes容器排空过程的三维CFD模拟A 3-D computational fluid dynamics model for forced air cooling of eggs placed in trays强迫空气冷却纸盘中鸡蛋的流体力学3-D计算模型A kinetic study of the release of vanillin encapsulated in Carnauba wax microcapsules香兰素封装在巴西棕榈蜡微胶囊中释放的动力学研究A machine vision system for identification of micro-crack in egg shell鉴别蛋壳细微裂缝的机器影像系统On the usage of acoustic properties combined with an artificial neural network – A new approach of determining presence of dairy fouling利用声学特性结合人工神经网络-鉴定乳产品存在污染的一种新方法A potentiometric electronic tongue for the discrimination of honey according to the botanical origin. Comparison with traditional methodologies: Physicochemical parameters and volatile profile根据原植物用电子舌的电位差区别蜂蜜.与传统方法:理化性参数和挥发性进行对比A rapid method to discriminate season of production and feeding regimen of butters based on infrared spectroscopy and artificial neural networks 一个基于红外光谱和人工神经网络来区分季节性生产和黄油供给方案的快速方法A review: Crispness in dry foods and quality measurements based on acoustic–mechanical destructive techniques评审:基于声音仪器的破坏性试验对干燥食品酥脆度和质量的测量Aeration of model gels: Rheological characteristics of gellan and agar gels凝胶通气模式:结冷胶和琼脂凝胶的流变学特性Agglomeration of durum wheat semolina: Thermodynamic approaches for hydration properties measurements硬质小麦粗面粉的凝聚:热力学方法对于水合性能的测量Alleviating bottlenecks in a microbiology laboratory减少在微生物实验室中的瓶颈Effect of the amount of steam during baking on bread crust features and water diffusion面包在烘烤期间蒸汽对面包表皮特征和水扩散的影响An enzyme sensor for the determination of total amines in dry-fermented sausages一种酶传感器在腊肠风干发酵中对总有机胺的决定性An improved model of the seeded batch crystallization of glucose monohydrate from aqueous solutions从含水的溶解液中分批处理去籽的结晶化葡萄糖一水合物的一种改良模式An RFID application in the food supply chain: A case study of convenience stores in Taiwan无线射频识别在食品供应链中的应用:台湾便利储藏的案例研究Analytical model for variable moisture diffusivity estimation and drying simulation of shrinkable food products分析模型对可变湿度扩散性的估计和可收缩食品的干燥模拟Anthocyanin degradation kinetics during thermal and high pressure treatments of raspberries红草莓在高压和热处理下花青素退化的动力学Application of hybrid image features for fast and non-invasive classification of raisin图像特征混合对葡萄干快速和非侵入分类的应用Application of NIR hyperspectral imaging for discrimination of lamb muscles近红外高光谱对识别羔羊肌肉的应用Aqueous extraction of anthocyanins from Hibiscus sabdariffa: Experimental kinetics and modeling从洛神花中萃取花青素的实验历程和建模Aseptically packaged UHPH-treated apple juice: Safety and quality parameters during storage无菌包装超高压均质处理苹果汁:储藏中的安全与质量参数Automatic freshness assessment of cod (Gadus morhua) fillets by Vis/Nir spectroscopy利用可见近红外光谱对鳕鱼(大西洋鳕)鱼片新鲜度的自动评估Beer quality screening by FT-IR spectrometry: Impact of measurement strategies, data pre-processings and variable selection algorithms傅里叶变换红外光谱学光谱测定法对啤酒品质的筛选:测量方法,数据预处理和多变的算法选择对测量的影响Calcium effect on mechanical properties of model cell walls and apple tissue钙对典型细胞壁和苹果组织机械性能的作用CFD model development and validation of a thermonebulisation fungicide fogging system for postharvest storage of fruit热雾化杀菌剂系统对采收后食品储藏计算流体动力学模型的发展和确立Changes in orange juice characteristics due to homogenization and centrifugation橘子饮料特性因均化作用和离心分离所出现的变化Characterization and antimicrobial activity studies of polypropylene films with carvacrol and thymol for active packaging聚丙烯薄膜附加香芹酚和百里香酚对活性包装的表征和抗菌活性研究Characterization of bread dough: Rheological properties and microstructure面包面团的特性表述:流变性能和微观结构Coffee beans microstructural changes induced by cultivation processing: An X-ray microtomographic investigation种植加工引诱咖啡豆微观结构的变化:X射线微观层析成象的调查Combination of digital images and laser light to predict moisture content and color of bell pepper simultaneously during drying在干燥情况下,利用数字图像和激光灯的结合对灯笼椒的水分含量和颜色同时进行预测Comparative study of film forming behaviour of low and high amylose starches using glycerol and xylitol as plasticizers利用丙三醇和木糖醇作为增塑剂在高低直链淀粉质食品薄膜形成状况的对比性研究Comparison of total milk-clotting activity measurement precision using the Berridge clotting time method and a proposed optical method对比利用贝里奇凝固时间的方法和拟议光学方法对牛奶凝固活度的测量精度Compressive textural attributes, opacity and syneresis of gels prepared from gellan, agar and their mixtures压缩性组织的特性,从结冷胶,琼脂以及它们的混合物中凝胶准备的不透明度和脱水收缩作用Computer simulation model development and validation for radio frequency (RF) heating of dry food materials无线电频率对干燥食物材料加热的计算机模拟模型的发展和验证Crispiness of a microwave-expanded imitation cheese: Mechanical, acoustic and sensory evaluation微波扩大人造干酪的松脆物:力学,声学和感官评价Classification of black tea liquor using cyclic voltammetry利用循环伏安法对红茶白酒的分类Determination and removal of malondialdehyde and other2-thiobarbituric acid reactive substances in waste cooking oil检测和去除废弃食用油中丙二醛和其他2-硫代巴比土酸的反应物Determination of anthocyanin concentration in whole grape skins using hyperspectral imaging and adaptive boosting neural networks利用高光谱影像和适应促进神经网络测定全部葡萄皮中花青素浓度Determination of translucent content in mangosteen by meansof near infrared transmittance利用近红外透光率的方法对山竹果透明率的检测Development of a novel method to measure the film thickness of cured can coatings一个对腌罐头镀膜薄膜厚度测定新方法的发展Dielectric properties of sea cucumbers (Stichopus japonicus ) and model foods at 915 MHz典型食品和海参(刺参)在915MHz下的介电性能DMA peaks in potato cork tissue of different mealiness动态力学分析法在不同粉性的土豆软木组织的应用Influence of drying and hydrothermal treatment of corn on the denaturation of salt-soluble proteins and color parameters干燥和热处理玉米在可溶性盐蛋白和颜色参数变性上的影响Drying characteristics of mango slices using the Refractance Window™ technique芒果切片的干燥特性在折射窗薄层干燥技术上的应用Drying kinetics using superheated steam and quality attributes of dried pork slices for different thickness, seasoning and fibers distribution干燥动力学利用干燥猪肉切片的过热蒸汽和品质特性对不同厚度,风干和纤维分布的应用Dynamic oscillatory rheological measurement and thermal propertiesof pea protein extracted by salt method: Effect of pH and NaCl利用盐法对豌豆蛋白萃取的动态震荡流变测量和热性能:PH和盐的作用Dynamic oscillatory shear properties of O/W model system meat emulsions: Linear viscoelastic analysis for effect of temperature and oil concentration on protein network formation油水比率的动态振动剪切性能模型系统肉乳剂:线性粘弹性分析对温度和含油浓度在蛋白质网状形成的影响Effect of dimensions and geometry of co-field and co-linear pulsed electric field treatment chambers on electric field strength and energy utilization在电场强度和能量利用上共线性和共面性电场脉冲处理chambers的尺寸规模和几何体的影响Effect of high or low molecular weight of components of feed on transmembrane flux during forward osmosis促进渗透期间以跨膜通量为能源成分的分子量的高或低的影响Effect of morphology on water sorption in cellular solid foods. Part II: Sorption in cereal crackers水吸附在多细胞固体食品形态学的影响第二部分:吸附谷类饼干的吸附Effect of morphology on water sorption in cellular solid foods.Part I: Pore scale network model水吸附在多细胞固体食品形态学的影响第一部分:气孔比例网状模型Effect of salt and sucrose content on dielectric properties and microwave freeze drying behavior of re-structured potato slices盐和蔗糖含量对土豆切片复合组织介电性能和微博冷冻干燥的影响Effect of some operating variables on the microstructure and physical properties of a novel Kefir formulation一些运行变量对新克菲尔构想的微观结构和物理性能的影响Effects of electroplasmolysis treatment on chlorophyll and carotenoid extraction yield from spinach and tomato电质壁分离对菠菜和番茄中叶绿素和类胡萝卜素提取率的影响Effects of vacuum frying on structural changes of bananas真空油炸对香蕉结构变化的影响A finite element model for mechanical deformation of single tomato suspension cells一种对于单一番茄悬浮细胞的机械变形的有限元模式Enhanced survival of spray-dried microencapsulated Lactobacillus rhamnosus GG in the presence of glucose提高在葡萄糖前将装入乳酸菌鼠李糖GG的微胶囊进行喷雾干燥的残余物Enzymatic browning in sliced and puréed avocado: A fractal kinetic study 鳄梨和切片中的酶促褐变:一种分形动力学研究Enzyme inactivation kinetics and colour changes in Garlic (Allium sativum L.)blanched under different conditions在不同条件下大蒜变白中酶失活动力学和颜色的变化Evaluating banana ripening status from measuring dielectric properties利用介电性能测量香蕉成熟状况的评估Evaluating non-stick properties of different surface materials for contact frying不同表面材料的非粘性对接触油炸的评估Evaluation of Photoshop software potential for food colorimetry Photoshop软件对食品比色法可能性的评估Fast determination of boiling time of yardlong bean using visible and near infrared spectroscopy and chemometrics利用可见和近红外光谱学以及化学计量学快速测定长豇豆的沸腾时间Feasibility of NIR spectroscopy for non-destructive characterizationof table olive traits近红外光谱对表橄榄特性无损检测的可行性Food supply chain leanness using a developed QFD model食品供给链缺乏使用一种成熟的质量功能展开模式Fractal analysis of the retrogradation of rice starch by digital image processing利用数字图像处理米粉糊液凝沉的分形分析Frequency- and temperature-dependent dielectric properties of fruit juices associated with pasteurization by dielectric heating利用电介质加热杀菌法与果汁中与温度和频率有关的介电性能的相关性Development of a rapid, non-destructive method for egg contentdetermination in dry pasta using FT-NIR technique利用傅里叶变红外光谱技术测量鸡蛋内部的一种快速无损检测方法的发展Gelation properties of chicken myofibrillar protein induced by transglutaminase crosslinking利用转谷氨酰胺酶交联诱导鸡肉肌原纤维蛋白的胶凝特性Generalized microstructural change and structure-quality indicators of a food product undergoing different drying methods and conditions一种食品经过不同条件下和不同干燥方法的一般性微观结构变化和结构性能质量指标Glass transition phenomenon on shrinkage of papaya during convective drying木瓜在对流干燥期间玻璃转化现象的收缩Effect of saccharides on glass transition temperatures of frozen and freeze dried bovine plasma protein糖类在冷冻和冻结干燥牛血浆蛋白的玻璃转化温度的影响Heat transfer modelling in a refrigerated display cabinet: The influence of operating conditions冷藏展示柜的热传递模型:操作条件的影响Specific volume and compressibility measurements of tomato pasteat moderately high pressure as a function of temperature番茄酱在适当高压下作为温度函数比容和可压缩性测量Hybrid mixture theory based moisture transport and stress development in corn kernels during drying: Coupled fluid transport and stress equations基于在干燥期间玉米粒水分运输和压力发展的杂交混合理论:耦合流体运输和压力方程式Hydrodynamic, thermo-analytical and molecular structural investigations of enzyme interesterified oil and its thermo-oxidative stabilityby thermogravimetric analysis利用热重量分析对酯化油和其热氧化稳定的流体力学,热解析和分子结构的分析Classification of fresh Atlantic salmon (Salmo salar L.) fillets stored under different atmospheres by hyperspectral imaging利用高光谱影像对新鲜大西洋鲑鱼切片在不同气压下储藏的分类Imaged based estimation of food volume using circular referentsin dietary assessment饮食评估中食品体积的估计使用循环参照物的影像基础Quality classification of cooked, sliced turkey hams using NIR hyperspectral imaging system利用近红外高光谱影像系统对熟火鸡火腿切片的品质分级Implication of water activity and glass transition on the mechanicaland optical properties of freeze-dried apple and banana slices水活性和玻璃转化在冷冻干燥苹果和香蕉切片的力学光学性能的含义Inactivation of Saccharomyces cerevisiae in pineapple, grape and cranberry juices under pulsed and continuous thermo-sonication treatments酿酒酵母在菠萝,葡萄和蔓越橘汁脉冲和连续热声波降解法处理下的失活Investigating the performance of thermo nebulisation fungicide fogging system for loaded fruit storage room using CFD model利用流体力学模型计算热雾化杀菌剂雾化系统对已装水果储藏室性能的研究An Exploration of Why People Participate in Second Life Social Support Groups关于人们参加第二人生社会扶持组织原因的探索Kinetics of quality changes of pumpkin (Curcurbita maxima L.) stored under isothermal and non-isothermal frozen conditions南瓜储藏在等温和非等温冷冻条件下动力学性能的变化Kinetics studies during NaCl and KCl pork meat brining猪肉盐浸处理中氯化钠和氯化钾的动力学研究Linear and non-linear viscoelastic behaviors of crosslinked tapioca starch/polysaccharide systems交联木薯淀粉/多糖系统的线性和非线性粘弹性行为Monitoring changes in feta cheese during brining by magnetic resonanceimaging and NMR relaxometry在浸盐作用期间利用磁共振影像和核磁共振弛豫时间监测羊奶酪的变化Mathematical model of pork slice drying using superheated steam利用过热蒸汽干燥猪肉切片的数学模型Mathematical modeling of intermittent and convective drying of rice and coffee using the reaction engineering approach (REA)利用反作用工程方法间歇性和对流干燥大米,咖啡的数学建模Mathematical modeling of swelling in high moisture whey protein gels膨胀高水分乳清蛋白凝胶的数学建模Mathematical modeling of the heat and mass transfer in a stationary potato sphere impinged by a single round liquid jet in a hydro fluidization system利用单轮液体喷射在水电流态化系统在高温和质量传递在静止土豆表面撞击的数学建模An approach for the enhancement of the mechanical properties and film coating efficiency of shellac by the formation of composite films based on shellac and gelatin利用基于虫胶和明胶复合薄膜形成对虫胶的镀膜效率和机械性能提高的方法Mechanical relaxation times as indicators of stickiness in skimmilk–maltodextrin solids systems机械力松弛时间作为在粘性表层物牛奶麦芽糖糊精固体系统的指标Effect of composition on the mechanical response of agglomeratesof infant formulae初期公式的附聚物的机械回应成分的影响Combination of optical and non-destructive mechanical techniquesfor the measurement of maturity in peach光学和无损机械技术组合对桃子成熟的测量Expansion mechanism of extruded foams supplemented with wheat bran 增补挤压泡沫体伴随麦麸的膨胀原理Mechanistic model of in vitro salt release from model dairy gels based on standardized breakdown test simulating mastication乳品凝胶基于模拟粉碎稳定性试验标准在使观众盐释放的机械模型Mechanistic model to couple oxygen transfer with ascorbic acid oxidation kinetics in model solid food在固体食品模型中机械模型对结合氧运输随着抗坏血酸氧化的动力学Effect of sugar, citric acid and egg white type on the microstructuraland mechanical properties of meringues调和蛋白的糖,柠檬酸和蛋白类型在微观结构和机械性能的影响Microstructure and mechanical properties of soy protein/agar blend films: Effect of composition and processing methods大豆蛋白和琼脂膜混合的微观结构和机械性能:成分和处理方法的影响Coffea arabica beans microstructural changes induced by roasting: AnX-ray microtomographic investigation利用烘烤引诱咖啡豆微观结构的变化:一种X射线微层析调查The impact of microwave heating of infant formula model on neo-formed contaminant formation, nutrient degradation and spore destruction初级理论模型在新成立的污染物形成的微波加热的影响:营养退化和孢子退化Modeling and experimental validation of mass transfer from carbonated beverages in polyethylene terephthalate bottles从碳酸饮料在聚对苯二甲酸乙二醇酯瓶子中质量传递的实验验证和建模Modeling microbial kinetics as a function of temperature: Evaluationof dynamic experiments to identify the growth/inactivation interface根据温度对微生物动力学建模:动态实验的评估来鉴定增长/失活的分界面Modeling rehydration of porous food materials: I. Determinationof characteristic curve from water sorption isotherms多孔渗水食品材料的再水化建模:1,水等温吸附线中特性曲线的测定Modeling rehydration of porous food materials: II. The dual porosity approach多孔渗水食品材料的再水化建模:2,双重多孔性方法Modeling the effects of initial nitrogen content and temperatureon fermentation kinetics of hard cider初始含氮量和温度在苹果酒的发酵动力学的建模作用Modelling flow behaviour of dairy foams through a nozzle乳品泡沫通过喷嘴的建模流动状况Modelling of coupled heat and mass transfer during a contact baking process在联系烘烤进程期间耦合高温和质量传递的建模Monitoring and grading of tea by computer vision – A review利用计算机视觉对茶叶监测和分级-一个评审Monitoring of ATP and viable cells on meat surface by UV–Vis reflectance spectrum analysis利用紫外-可见反射比光谱分析对肉表面ATP和活细胞的监测Monitoring the dynamic density of dough during fermentation using digital imaging method利用数字影像方法在发酵期间对生面团的动态密度监测Microwave puffing: Determination of optimal conditions using a coupled multiphase porous media – Large deformation model微波膨化:利用一种耦合多相多孔介质对最适条件的测定-大型变形模型Red to far-red multispectral fluorescence image fusion for detection offecal contamination on apples利用红色对远红外多谱线的荧光影像融合对苹果排泄污染物的检测Artificial neural network model for prediction of cold spot temperature in retort sterilization of starch-based foods人工神经网络模型对淀粉性食物的蒸煮杀菌的冷点温度的预测Non-destructive analysis of anthocyanins in cherries by means of Lambert–Beer and multivariate regression based on spectroscopy and scatter correction using time-resolved analysis利用Lambert–Beer和多元回归基于光谱学和散射修正使用时间分辨分析对樱桃花青素的无损检测分析Non-destructive internal quality assessment of ‘‘Hayward’’ kiwifruitby waveguide spectroscopy利用波导光谱学对“Hayward”猕猴桃的内部品质无损检测Non-destructive maturity classification of mango based on physical, mechanical and optical properties基于物理,机械和光学特性对芒果成熟等级的无损检测Non-destructive prediction of hardening pericarp disorder in intact mangosteen by near infrared transmittance spectroscopy利用近红外线透射比光谱学对完整的山竹果无序表皮樱花的无损检测Efficacy of non-thermal technologies and sanitizer solutions on microbial load reduction and quality retention of strawberries非热能技术和食品防腐剂解决方案对草莓的微生物负荷减低和质量保持的功效Numerical modeling of heat and mass transfer during coffee roasting process咖啡豆烘烤进程的高温和质量传递数值模拟Accelerated inactivation of Geobacillus stearothermophilus spores by ohmic heating利用欧姆加热对芽孢杆菌的加速钝化Optimisation of total phenolic acids extraction from mandarin peels using microwave energy: The importance of the Maillard reaction利用微波能量从柑橘果皮对酚酸萃取的优化:美拉德反应的重要性Effect of guar gum content on some physical and nutritional properties of extruded products瓜尔豆胶在挤压产品的一些物理和营养特性的作用Physical properties of acerola and blueberry pulps金虎尾和蓝莓果肉的物理特性Physico-chemical characterization of chitosan-based edible films incorporating bioactive compounds of different molecular weight不同分子量的壳聚糖基可食用薄膜合并生物活性的化合物的理化特性Predicting cleaning time of ventilation duct systems in the food industry 通风管系统在食品工业的清洗时间预测Prediction of beef quality attributes using VIS/NIR hyperspectral scattering imaging technique利用可见/近红外高光谱散射影像技术队牛肉质量特性的预测Prediction of colloidal stability in white wines using infrared spectroscopy利用红外线光谱学对白葡萄酒胶体稳定性的预测Prediction of dry mass glass transition temperature and the spray drying behaviour of a concentrate using a desorption method利用解析方法对浓缩的干质量玻璃化温度和喷雾干燥状况的预测Production, recovery and applications of xanthan gum by Xanthomonas campestris利用白菜黄单胞菌对黄原胶的生产,恢复和应用Pulsed electric field assisted aqueous extraction of colorants from red beet电场脉冲协助红甜菜中色素的萃取Investigation of Raman chemical imaging for detection of lycopene changes in tomatoes during postharvest ripening利用拉曼化学成像在采收后成熟期间对番茄红素变化的检测的调查研究Real-time modeling of milk coagulation using in-line near infrared spectroscopy利用管线式近红外光谱学对牛奶凝结的即时性建模Removal of residual pesticide, fenitrothion, in vegetables by using ozone microbubbles generated by different methods用不同方法利用臭氧微气泡的产生对蔬菜杀虫剂(杀螟松)残渣的去除Effect of temperature on dynamic and steady-state shear rheological properties of siriguela (Spondias purpurea L.) pulp温度对松果菊果肉的动态和稳态切变流变学的影响Rheological behavior and stability of D-limonene emulsions made by a novel hydrocolloid (Angum gum) compared with Arabic gum由一种相比阿拉伯树胶的新水状胶体(Angum胶)制成的D-柠檬烯乳胶的流变特性和稳定性Modeling and estimation of rheological properties of food productsfor manufacturing simulations食品的流变特性对于制造模型的建模和评估Rheological, textural and spectral characteristics of sorbitol substituted mango jam山梨醇替代芒果果酱的流变的,组织的和光谱特性Rheology and microstructure of myofibrillar protein–plant lipid composite gels: Effect of emulsion droplet size and membrane type肌原纤维蛋白-植物油脂附和凝胶剂的流变学特性和微观结构:乳滴尺寸和薄膜类型的影响Rheometric non-isothermal gelatinization kinetics of mung bean starchslurry: Effect of salt and sugar – Part 1绿豆淀粉泥浆的流变测定非等温凝胶化动力学:盐和糖的作用-第一部分Scale-up unit of a unique moderately high pressure unit to enhance microbial inactivation唯一适度高压单元的增大单元来提高微生物失活Particle surface moisture content estimation using population balance modeling in fluidised bed agglomeration利用平衡建模的数量对使底座结块液化微粒表面水分含量的估测Shelf life prediction of aluminum foil laminated polyethylene packed vacuum dried coconut milk powder铝箔聚乙烯分层包装真空干燥椰子汁粉保质期的预测Effect of modified atmosphere and active packaging on the shelf-lifeof fresh bluefin tuna fillets改良环境和有效包装在新鲜金枪鱼切片保质期的影响Shortwave infrared hyperspectral imaging for detecting sour skin (Burkholderia cepacia)-infected onions短波红外线高光谱影像对被感染洋葱皮发酵的测定Wavelength selection in vis/NIR spectra for detection of bruises on apples by ROC analysis利用ROC分析用可见/近红外光谱对苹果损伤测定波长的选择Maltodextrin/pectin microparticles by spray drying as carrier fornutraceutical extracts喷雾干燥利用麦芽糖糊精/果胶微粒作为载体对保健品提取Structural properties of freeze-dried rice经过冷冻干燥大米的结构特性Study of contact angle, wettability and water vapor permeability in carboxymethylcellulose (CMC) based film with murta leaves(Ugni molinae Turcz) extract基于murta叶片薄膜萃取羧甲基纤维素接触角,湿润度和水蒸气渗透性的研究Granularity and its importance for traceability in a farmed salmon supply chain间隔尺寸以及其重要性对于养殖鲑鱼供给链的可追溯性Texture prediction during deep frying: A mechanistic approach油炸期间的质地预测:一种机械型工作设计方法The influence of vacuum impregnation on the fortification of apple parenchyma with quercetin derivatives in combination with pore structures X-ray analysis苹果软细胞组织附和橡黄素衍生物与X-射线孔隙结构分析结合的真空浸渍在营养强化上的影响The potential of electrospraying for hydrophobic film coating on foods 电喷镀对于在食品疏水性薄膜敷层的可能性The use of biodosimetry to measure the UV-C dose delivered to a sphere,and implications for the commercial treatment of fruit利用生物计量测定法测定紫外-C线剂量传递到球面,对于水果商业化处理的影响Corrigendum to ‘‘Theoretical and experimental analyses of drop deformation and break-up in a scale model of a high-pressure homogenizer’’ [Journal of Food Engineering 103/1 (2010) 21–28]勘误表:“高压均质器的液滴变形和终止缩尺模型的理论和实验分析”[食品工程杂志103/1(2010)21-28]Development of a two-band spectral imaging system for real-time citrus canker detection双频段光谱影像对于即时性检测柑橘溃疡的发展Shape determination of horticultural produce using two-dimensional computer vision – A review利用二维计算机影像对园艺产品形状的检测-一份评审Comparative study of high intensity ultrasound effects on foodproteins functionality高强度超声波作用在食物蛋白功能的对比性研究Uncertainty and sensitivity analysis: Mathematical model of coupled heat and mass transfer for a contact baking process不确定性和灵敏度分析:耦合高温和质量传递对于联系烘烤进程的数学模型Variable selection in visible and near-infrared spectra: Application toon-line determination of sugar content in pears可见和近红外光谱的可变性选择:应用于梨含糖量的即时检测Application of visible and near infrared spectroscopy for rapidand non-invasive quantification of common adulterants in Spirulina powder可见和近红外光谱对于螺旋藻粉共同掺杂物的快速以及非侵入性定量的应用Classification of longan fruit bruising using visible spectroscopy利用可见光谱学对桂圆损伤的分类Water diffusion and enzyme activities during malting of barley grains: A relationship assessment在大麦谷粒的麦粒发芽期间水扩散和酶活性:一个相关性评估Water transport properties of artificial cell walls人造细胞壁的水运输性能Weight loss of frozen bread dough under isothermal and fluctuating temperature storage conditions冷冻面包面团在等温和变动温度储藏条件下的质量损失Automated fish bone detection using X-ray imaging利用X-射线影像对鱼骨的自动化检测X-ray microtomography to study the microstructure of mayonnaiseX-射线显微断层显像对蛋黄酱微观结构的研究Influence of yeast and frozen storage on rheological, structural andmicrobial quality of frozen sweet dough酵母和冷冻储藏对冷冻甜面团的流变性,结构和微生物质量的影响Yield improvement in progressive freeze-concentration by partial melting of ice通过冷冻食品局部融化利用逐步冷冻浓缩提高产量。
血管内皮生长因子和缺氧诱导因子对软骨细胞凋亡的作用
血管内皮生长因子和缺氧诱导因子对软骨细胞凋亡的作用周建林;方洪松;彭昊;邓爽;翁金清;刘丰;陈森;周观金【摘要】BACKGROUND:Osteoarthritis is a joint disease that primarily affects the cartilage. With the changes of the extracelular matrix, chondrocytes appear to have apoptosis. Vascular endothelial growth factor plays an important role in promoting endothelial cel division and proliferation and inducing angiogenesis. Hypoxia-inducible factor is a celular transcription factor and produces different reactions due to the oxygen content. Vascular endothelial growth factor and hypoxia-inducible factor are focused on inhibiting chondrocyte apoptosis. OBJECTIVE:To elaborate the effects of vascular endothelial growth factor and hypoxia-inducible factors on chondrocyte apoptosis. METHODS: Recent literatures related to chondrocyte apoptosis were summarized and analyzed. During the process of osteoarthritis, changes in vascular endothelial growth factors in chondrocytes and regulatory effects of vascular endothelial growth factor and hypoxia-inducible factor on chondrocyte apoptosis were elaborated.%背景:骨关节炎是一种关节疾病,主要影响软骨,随着软骨细胞胞外基质的变化,软骨细胞发生凋亡,血管内皮生长因子在促进血管内皮细胞分裂与增殖、诱导血管生成中起重要作用。
地塞米松对肺纤维化小鼠细胞因子及羟脯氨酸的影响
地塞米松对肺纤维化小鼠细胞因子及羟脯氨酸的影响史可云;谢婧【摘要】Objective To observe the effect of dexamethason on the levels of IFN - γ,IL-rn4 and TNF -α in serum and explore pathological structure of lung tissue in BLM - induced pulmonary fibrosis rats. Methods Thirty mice were divided randomly into normal,model,and dexamethason groups. Pulmonary fibrosis model was established by injection of bleomycin (BLM) via trachea (5 mg/kg). After 24 h,rats were given drugs by ig in all groups once a day. On the 14th and 28th day,6 mice were killed and the lungs were collected for observing pathological structure of lung tissue by HE staining. Interleukin -4(IL-4),interferon gamma (IFN-γ) and tumor necrosis factor -α(TNF - α) in serum and hydroxyproline (HYP)content were detected by enzyme linked immunosorbent assay (ELISA). Results Compared with the normal group,IFN -y content was significantly lowered,while IL-4 and TNF-α considerably increased in the model group (P<0. 05). Compared with the model group,IFN -γcontent was significantly elevated (P<0.05) and IL-4,TNF-α levels significantly decreased(P<0. 05). The degree of fibrosis was alleviated in Astragalus decoction and Astragalus polysaccharide groups (P < 0. 05). Conclusion Astragalus polysaccharides have protective effect by regulating pulmonary fibrosis in rat I /II type cytokines balance and TNF - α level,thereby interfering with the occurrence of pulmonary interstitial fibrosis and development.%目的观察肺纤维化小鼠血清中IFN -γ、IL-4、TNF -α的含量、生化指标,探讨地塞米松干预治疗肺纤维化的作用机理.方法昆明小鼠30只随机分为空白组、博莱霉素(BLM)组、地塞米松(DXM)组.采用气管内注入BLM复制肺纤维化模型,造模后第2天使用地塞米松药物干预治疗,第14天采用酶联免疫吸附法测定血清IFN -γ、IL-4、TNF-α及羟脯氨酸(HYP)含量.结果与空白组相比较,BLM组大鼠血清IFN -γ含量降低,IL-4、TNF-α的含量升高(P<0.05),BLM 组各时间点Hyp含量有明显增加(P <0.01).DXM与BLM组Hyp相比较,Hyp含量于第14天和第28天有明显下降(P <0.05).结论应用地塞米松可以明显减轻大鼠肺纤维化进程,不仅降低Ⅱ型细胞因子(IL -4)含量,而且升高Ⅰ型细胞因子(IFN -γ)及TNF-α含量,从而调整Ⅰ型/Ⅱ型细胞因子平衡及TNF-α表达抗纤维化作用.【期刊名称】《实用临床医药杂志》【年(卷),期】2012(016)015【总页数】3页(P17-19)【关键词】肺纤维化;地塞米松;细胞因子;羟脯氨酸【作者】史可云;谢婧【作者单位】江苏省宜兴人民医院内科,江苏宜兴,214200;江苏省宜兴人民医院内科,江苏宜兴,214200【正文语种】中文【中图分类】R563特发性肺纤维化(IPF)是一种由免疫介导的炎症性疾病。
CFDA SE (细胞增殖示踪荧光探针) 说明书
CFDA SE (细胞增殖示踪荧光探针) 产品编号产品名称包装C1031 CFDA SE (细胞增殖示踪荧光探针) 5mg产品简介:CFDA SE 的全称为Carboxyfluorescein diacetate, succinimidyl ester ,是一种近年来被广泛应用的细胞增殖检测用荧光探针,也可以用于细胞的荧光示踪。
基于CFDA SE 荧光标记的细胞增殖检测和[3H]-thymidine 掺入、BrdU 标记获得的检测结果完全一致,但同时可以提供更多的细胞增殖信息。
使用CFDA SE 检测可以提供整个细胞群中有多少比例的细胞分裂了1次、2次或更多次数,同时如果和其它荧光探针联用,可以获取不同分裂次数细胞的其它相关信息。
CFDA-SE 的分子式为C 29H 19NO 11,分子量为557.47,CAS number 为150347-59-4。
CFDA SE 可以通透细胞膜,进入细胞后可以被细胞内的酯酶(esterase)催化分解成CFSE ,CFSE 可以偶发性地(spontaneously)并不可逆地和细胞内蛋白的Lysine 残基或其它氨基发生结合反应,并标记这些蛋白。
在加入荧光探针CFDA SE 后大约24小时,即可充分标记细胞。
被CFDA SE 标记的非分裂细胞的荧光非常稳定,稳定标记的时间可达数个月。
CFDA SE 标记细胞的荧光非常均一,比以前使用的其它细胞示踪荧光探针例如PKH26的荧光更加均一,并且分裂后的子代细胞的荧光分配也更均匀。
由于CFDA SE 标记细胞的荧光非常均匀和稳定,每分裂一次子代细胞的荧光会减弱一半,这样通过流式细胞仪检测就可以检测出没有分裂的细胞,分裂一次的细胞(1/2的荧光强度),分离两次的细胞(1/4的荧光强度),分裂三次的细胞(1/8的荧光强度)以及类似的其它分裂次数的细胞。
采用CFDA SE 通过流式细胞仪检测获得的检测结果参考右图。
每一个峰代表一种分裂次数的细胞,从右至左的峰通常依次为分裂0次、1次、2次、3次等次数的细胞。
鲁棒性优化的原理、评估方法及应用-放射医学论文-基础医学论文-医学论文
鲁棒性优化的原理、评估方法及应用-放射医学论文-基础医学论文-医学论文——文章均为WORD文档,下载后可直接编辑使用亦可打印——摘要:质子治疗过程容易受射程偏差、摆位偏差、患者解剖结构改变等不确定因素的影响,质子调强放疗的鲁棒性优化是将这些不确定因素考虑进计划的制定过程中,增加治疗计划鲁棒性的一种方法,在临床中有广泛的应用。
鲁棒性优化的方法主要有4种:(1)概率法;(2)最差剂量法;(3)添加约束项;(4)多CT优化。
本文综述了这4种方法的原理、优缺点和临床应用情况。
同时,还介绍了治疗计划鲁棒性的评估方法。
虽然目前剂量体积直方图束是最常用的评估治疗计划鲁棒性的方法,但是,剂量体积直方图束不能反映质子调强放疗计划对解剖结构改变的鲁棒性,因此,还急需建立一个简单易用并能被广泛接受的鲁棒性评估方法,方便质子调强放疗计划的对比和评估。
关键词:质子调强放射治疗; 鲁棒性优化; 鲁棒性评估; 综述;Abstract:The intensity modulated proton therapy(IMPT)process is susceptible to factors such as range uncertainties, setup uncertainties and anatomical changes. The robust optimization of IMPT is a method to increase the robustness of treatment plan by taking these uncertainties into consideration in the process of optimization, which is widely used in clinical practice.There are four methods for robust optimization:(1)probability method;(2)worst dose method;(3)adding constraints;(4)multiple CT optimization. This paper reviews the principles, advantages and disadvantages of these four methods and their clinical application, and it also introduces the evaluation methods for robustness. Although the dose volume histogram(DVH)bands is the most commonly used method to evaluate the plan robustness, DVH bands cannot reflect the robustness of IMPT plan with anatomical changes. Therefore, it is urgent to establish a simple and widely accepted robustness evaluation method to facilitate the comparison and evaluation of IMPT plans.Keyword:intensity modulated proton therapy; robust optimization; robustness evaluation; review;前言质子调强放疗(Intensity Modulated Proton Therapy,IMPT)相比于传统的光子调强放疗(Intensity Modulated Radiation Therapy,IMRT)有剂量上的优势[1,2,3,4],但是,IMPT的剂量线梯度大,容易受不确定因素的影响[5]。
土壤微塑料影响植物生长的因素与机制研究进展
塑料作为一种被广泛应用的有机合成聚合物材料,在为我们生活提供便利的同时,也带来了后续的环境问题。
据估算,到2050年,将有大约12000万t 塑料垃圾被埋入垃圾填埋场或自然环境中[1],塑料垃圾进入到环境后会逐渐破碎变成微塑料(<5mm ),导致其在土壤和水体中的丰度逐年递增[2-3]。
2015年的第二届联合国环境大会已将微塑料污染列为环境与生态领域的第二大科学问题[3]。
目前,人们对水体中微塑料的认识已较为系统[4-6],土壤微塑料逐步成为新的研究热点[7-8]。
2012年Rillig [9]首次提出微塑料会影响土壤理化性质,这引起了人们对土壤微塑料的关注,后续研究表明微塑料可被植物吸收并积累[10-11],最终通过食物链进入人体。
厘清微塑料对植物生长的影响及其机制,有助于系统掌握其在土壤-植物体陈欣,郭薇,李济之,等.土壤微塑料影响植物生长的因素与机制研究进展[J].农业环境科学学报,2024,43(3):488-495.CHEN X,GUO W,LI J Z,et al.Research progress on the influencing factors and mechanisms of soil microplastics on plant growth[J].Journal of Agro-Environment Science ,2024,43(3):488-495.土壤微塑料影响植物生长的因素与机制研究进展陈欣1,郭薇1,2,李济之1,2,迟光宇1*(1.中国科学院沈阳应用生态研究所,污染生态与环境工程重点实验室,沈阳110016;2.中国科学院大学,北京100049)Research progress on the influencing factors and mechanisms of soil microplastics on plant growthCHEN Xin 1,GUO Wei 1,2,LI Jizhi 1,2,CHI Guangyu 1*(1.Key Laboratory of Pollution Ecology and Environmental Engineering,Institute of Applied Ecology,Chinese Academy of Sciences,Shenyang 110016,China ;2.University of Chinese Academy of Sciences,Beijing 100049,China )Abstract :Microplastics in soil can affect plant growth in a variety of ways,accumulate in plants,and eventually enter the human body via the food chain.Clarifying the mechanisms and main factors whereby microplastics influence plant growth can contribute to a systematic understanding of their environmental behavior in soil-plant systems.Both the occurrence state and physicochemical characteristics of microplastics can influence their effects on plants.In this paper,from the perspectives of particle size,shape,concentration,and type,plastic additives,and aging degree of microplastics,we review the main factors and mechanisms underlying the effects of soil microplastics on plant growth.The key direction of future research is proposed,which will provide a reference for further clarifying the impact of microplastics on soil ecosystems.Keywords :soil;microplastics;plant;influencing factor;mechanism of action收稿日期:2023-04-13录用日期:2023-06-19作者简介:陈欣(1968—),男,辽宁沈阳人,博士,研究员,研究方向为农业生态。
新型阻燃剂水滑石在EVA复合材料中的燃烧特性和阻燃性能
新型阻燃剂水滑石在EVA复合材料中的燃烧特性和阻燃性能杜隆超,瞿保钧*中国科学技术大学火灾科学国家重点实验室,高分子科学与工程系,合肥,230026 关键词:水滑石 EVA 无卤阻燃协效随着聚合物材料应用领域的不断扩大,由聚合物材料着火引起的重大火灾事故时有发生,这已引起了人们的普遍关注。
传统的聚合物阻燃大都是采用添加含卤的阻燃剂来实现。
这些含卤的阻燃聚合物材料虽然具有优良的阻燃性能,但是遇到火灾会产生大量的有毒烟雾和腐蚀性的卤化氢气体。
据报道,世界上因火灾事故而死亡的人中,80%以上是因为材料燃烧时散发出的烟雾和毒性气体使人窒息而死,而无卤阻燃剂,特别是无机氢氧化物阻燃剂具有极好的消烟作用,可以避免含卤阻燃材料燃烧时所释放出的大量有毒烟雾和腐蚀性气体,成为国际上阻燃材料的主要发展方向。
氢氧化镁和氢氧化铝阻燃剂是目前国内外无机阻燃剂中应用量最大,发展最快的两种。
水滑石是一类层状无机材料,兼有氢氧化镁和氢氧化铝类似的结构和组成,受热分解时释放大量水和二氧化碳,并吸收大量热,能降低燃烧体系的温度;分解释放出的水蒸汽和二氧化碳气体能稀释和阻隔可燃性气体,因此是很有希望的对环境友好的消烟型无毒无卤阻燃剂新品种。
然而,由于天然水滑石在自然界的分布非常有限,远不如氢氧化镁和氢氧化铝丰富,因此,本文在合成水滑石的基础上比较选择了与其粒径相同的氢氧化镁和氢氧化铝样品,利用锥板量热器,氧指数测定仪,热重分析仪等方法研究和比较了水滑石与氢氧化镁和氢氧化铝在EVA共聚物中的燃烧特性和阻燃性能,以及它与微胶囊化红磷(MRP)的协同阻燃效果。
1.EVA/水滑石复合材料的燃烧特性图1比较了阻燃剂含量为50 wt%时,EVA与水滑石,氢氧化镁,氢氧化铝复合材料的热释放速率(HRR)。
从图中可见,当无机阻燃剂加入后,材料的燃烧时间明显的延长,最大热释放峰值(PHRR)也极大的降低,而且燃烧曲线成双峰*联系人,E-mail:qubj@分布。
丛枝菌根真菌对番茄渗透调节物质含量的影响
园 艺 学 报 2007,34(1):147-152Acta Horticulturae Sinica丛枝菌根真菌对番茄渗透调节物质含量的影响贺忠群1,2,贺超兴23,张志斌2,邹志荣1,王怀松2,T UNDE Takacs3(1西北农林科技大学园艺学院,陕西杨凌712100;2中国农业科学院蔬菜花卉研究所,北京100081;3匈牙利科学院土壤科学与农业化学研究所,匈牙利布达佩斯H21022)摘 要:采用盆栽试验研究了不同浓度NaCl(015%和1%)胁迫下,接种丛枝菌根真菌(AMF)对番茄生长和渗透调节物质含量的影响。
结果表明:盐胁迫下,与未接菌番茄相比,接种AM F番茄能显著增加植株的生长,促进叶片和根系可溶性糖的积累,增加叶片可溶性蛋白含量及根系脯氨酸含量,使植株耐盐能力增强。
接菌株可溶性糖及可溶性蛋白的增加以及根系脯氨酸的大量积累在AM F提高番茄耐盐的渗透调节机制中具有重要的作用。
关键词:番茄;丛枝菌根真菌;NaCl胁迫;渗透调节物质中图分类号:S64112 文献标识码:A 文章编号:05132353X(2007)0120147206Study on O s m oti c Adjust m en t M echan is m of To ma to Sa lt Tolerance Enhanced by Arbuscul ar M ycorrh i za l Fung iHE Zhong2qun1.2,HE Chao2xing23,ZHANG Zhi2bin2,Z OU Zhi2r ong1,W ang Huai2s ong2,and T UNDE Takacs3(1D epart m ent of Horticulture,N orthw est A&F U niversity,Yangling,Shaanxi712100,China;2Institute of V egetables and Flo w2 ers,Chinese A cade m y of A gricultural Sciences,B eijing100081,China;3Research Institute of Soil Sciences and A gricultural Che m istry,Hungary A cade m y of Sciences,B udapest H21022,Hungary)Abstract:The effects of arbuscular mycorrhizal fungi(AMF)on p lant gr owth and os motic adjust m ent matter content of pot cultured t omat o under NaCl stress(015%and1%)were studied.The results showed that AMF2inoculati on significantly increased t omat o p lant gr owth,p r o moted the accumulati on of s oluble sugar in leaves and r oots,increased s oluble p r otein in leaves and p r oline content in r oots under salt stress,s o AMF enhanced salt t olerance of t omat o p lants.The accumulati on of s oluble sugar,s oluble p r otein and r oot p r oline induced by AMF p layed an i m portant r ole in os motic adjust m ent mechanis m of enhanced salt t olerance in my2 corrhizal t o mat o.Key words:T omat o;A rbuscular mycorrhizal fungi;NaCl stress;O s motic adjust m ent matter丛枝菌根真菌(A rbuscular mycorrhizal fungi,简写为AMF)对番茄的促生作用及提高番茄耐盐性的研究已有报道(L i et al.,1991a,1991b;Ruiz2Lozano&Azcon,1995;A l2Karaki et al.,2001;李敏等,2005)。
低氧增加人皮肤微血管内皮细胞系迁移并促进凋亡
低氧增加人皮肤微血管内皮细胞系迁移并促进凋亡程科;刘洪;张矛;赵渝;罗鸿;桂福强【摘要】Objective To study the effects of hypoxia on the cell migration,apoptosis and expression of related genes and proteins of human dermal microvascular endothelial cells(HDMEC). Methods To culture HDMEC in hypoxia condition by putting CoCl2in the cell incubator and all the subjects were divided to two groups which included normal group and hypoxia group.To find the appropriate CoCl2dose by CCK-8 experiment and the 200 μmol/L CoCl2was the best to establish hy poxia model.The migration of cells was measured by wound healingtest.Apoptosis rate was detec-ted by flow cytometry. The gene expressions were detected by RT-PCR and the protein levels were detected by West-ern blot. Results The migration ability of cells was enhanced in hypoxia condition (P<0.05). The apoptosis rate was increased in hypoxia condition(P<0.05).The gene expressions of HIF-1α,HIF-1β,VEGF,iNOS were increased comparing with normal groups depending on time(P<0.05).The protein expressions of HIF-1α,VEGF,iNOS were in-creased comparing with normal groups depending on time(P<0.05). Conclusions Cell migration, apoptosis of HDMEC were influenced by hypoxia. It may be explained by increasing expression of related gene and proteins like HIF-1α,VEGF,iNOS in hypoxia condition.%目的研究低氧环境对人皮肤微血管内皮细胞(HDMEC)迁移、凋亡及相关因子HIF-1α、VEGF、iNOS基因及蛋白表达的影响.方法低氧培养人微血管内皮细胞,分为常氧组(对照组)和低氧组(CoCl2模拟化学低氧).CCK-8细胞生存实验确定合适处理浓度(200 μ mol/L CoCl2),划痕实验检测细胞迁移能力,流式细胞技术观察细胞凋亡;用RT-PCR和 Western blot技术检测HIF-1α、VEGF、iNOS mRNA和蛋白表达.结果与常氧组比较,低氧组细胞迁移能力增加(P<0.05),凋亡增多(P<0.05),均呈时间依赖性.低氧组HIF-1α、HIF-1β、VEGF、iNOS mRNA表达较常氧组比较均增加(P<0.05),HIF-1α、VEGF、iNOS蛋白表达较常氧组比较均增加(P<0.05),具有一定时间依赖性.结论低氧能增强人皮肤微血管内皮细胞迁移能力,并促进其细胞凋亡,其可能机制与HIF-1α、VEGF、iNOS蛋白表达升高有关.【期刊名称】《基础医学与临床》【年(卷),期】2017(037)010【总页数】5页(P1429-1433)【关键词】低氧;低氧诱导因子1α;静脉性溃疡;人皮肤微血管内皮细胞【作者】程科;刘洪;张矛;赵渝;罗鸿;桂福强【作者单位】重庆医科大学附属第一医院血管外科,重庆400016;重庆医科大学附属第一医院血管外科,重庆400016;重庆医科大学附属第一医院血管外科,重庆400016;重庆医科大学附属第一医院血管外科,重庆400016;重庆医科大学附属第一医院血管外科,重庆400016;重庆医科大学附属第一医院血管外科,重庆400016【正文语种】中文【中图分类】R654在下肢静脉曲张(varicose veins)患者中,部分患者出现皮肤营养障碍,继而发生静脉性溃疡(venous ulcer)[1]。
【放射肿瘤基础研究】辐射的延迟效应启动脑微环境加速肿瘤生长
【放射肿瘤基础研究】辐射的延迟效应启动脑微环境加速肿瘤生长《Int J Radiat Oncol Biol Phys.》杂志 2018年8月29日在线发表美国华盛顿大学的 Duan C,Yang R , Yuan L 等撰写的实验研究论文《辐射的延迟效应启动脑微环境加速肿瘤生长Late Effects of Radiation Prime the Brain Microenvironment for Accelerated Tumor Growth 》。
(DOI: 10.1016/j.ijrobp.2018.08.033. )即便使用最高水准的手术切除、化疗和放疗等最先进的治疗手段,胶质母细胞瘤(GBM)仍然难以治愈。
GBM作为具有高度侵袭性( invasively)和难治性(aggressively)的表现型(phenotype)总是不断复发,大多数复发发生在放射治疗治疗野内。
虽然有大量关于原发胶质母细胞瘤GBM的文献报道,但是关于先前的照射如何改变复发肿瘤生长形式的全面研究还很缺乏。
作者复制放疗对脑微环境的延迟效应的动物模型及放疗复发胶质母细胞瘤进展的影响会是一个重大的进步。
作者对同一组小鼠分别接受0、20、30或40 Gy伽玛刀照射。
在辐照后6周将原始型(naive)未接受过照射的小鼠胶质母细胞瘤肿瘤细胞(DBT)植入同侧半球。
磁共振成像(MRI)测量肿瘤生长,监测体重下降评估动物存活率。
MRI结果支持H&E 组织学结果。
作者发现,未受过照射的小鼠胶质母细胞瘤肿瘤细胞原位植入到受过照射的小鼠大脑中所产生的肿瘤病灶远比将同样的细胞植入未接受过照射的小鼠大脑中所产生的肿瘤病灶更具有侵略性和难治性。
与对照组相比在接受过辐照的脑组织中的病变明显更大、坏死更明显、血管更丰富,周围具有侵袭性的肿瘤细胞增加,与复发高级别肿瘤患者常见的组织学特征一致。
作者认为,当原始型(之前未接受过辐照得)肿瘤细胞被殖入后,受到过照射的正常大脑业已存在的针对侵袭性肿瘤生长的细胞微环境就会启动。
模拟微重力对COL1A1-EGFP基因表达的影响
目录
缩略词.......................................................................................................................... 1 中文摘要...................................................................................................................... 3 Abstract ........................................................................................................................ 4 文献综述...................................................................................................................... 6 一 微重力对机体骨代谢的影响作用...................................................................... 6
分类号 UDC
中国农业大学硕士论文
密级
中国农业大学
硕士学位论文
模拟微重力对 COL1A1 EGFP 基因表达的影响
The Effect of Simulated Microgravity on the Expression of COL1A1-EGFP Gene
研究生 戴钟铨 导 师 刘 芃 芃 副教授
MiR-873对缺氧复氧诱导的心肌细胞凋亡的影响及其机制
ABSTRACT
Objective: To explore the role of miR-873 in cardiomyocyte injury induces by hypoxia
收稿日期(Date of reception):2018-07-14 第一作者(First author):周云洁,Email: yunjiezhhi@, ORCID: 0000-0003-1924-9642 通信作者(Corresponding author):周云洁,Email: yunjiezhhi@, ORCID: 0000-0003-1924-9642
[关键词] 微小RNA-873;心肌细胞;缺氧/复氧;凋亡;egl-9家庭缺氧诱导因子3
Effect of miR-873 on cardiomyocyte apoptosis induced by hypoxia reoxygenation and its mechanism
ZHOU Yunjie1, ZHANG Huichao2, SUN Zhixia3
858
KEY WORDS
ห้องสมุดไป่ตู้
中南大学学报 ( 医学版 ), 2019, 44(8)
reoxygenation (H/R) and its related mechanisms. Methods: H/R model was established by culturing mouse cardiac H9c2 cells in vitro, and miR-873 mimic was transfected. The experiments were divided into a control group, a H/R group, a negative control group and a miR-873 mimic group. The expression of miR-873 was measured using realtime PCR. The protein expression levels of egl-9 family hypoxia inducible factor 3 (Egln3), B-cell lymphoma-2 (Bcl-2) and Bcl-2 associated X protein (Bax) were evaluated by Western blotting. Cell apoptosis ELISA kit and cysteine-containing, aspartate-specific proteases-3 (caspase-3) activity kit was used to detect cell apoptosis and caspase-3 activity, respectively. The targeting effect of miR-873 on Egln3 were examined by the dual luciferase report gene assay, and the experiments were divided into a negative control group, a Egln3 3'-untranslated regions (3’-UTR) WT group (WT group) and a Egln3 3'-UTR MUT group (MUT group). In order to further detect the effects of Egln3 on miR873 mimics, the Egln3 overexpressed cells were constructed, and the experiments were divided into a H/R group, a H/R+miR-873 mimic group, a H/R+pcDNA3-Egln3 (pcEgln3) group and a H/R+ miR-873 mimic+pcEgln3 group. Results: Compared with the control group, the expression level of miR-873 was significantly decreased in the H/R group (P<0.05). Compared with the H/R group, H9c2 cell apoptosis, caspase-3 activity and the ratio of Bax/Bcl-2 were significantly reduced in the miR-873 mimic group (all P<0.05). Compared with the negative control group, the luciferase activity was significantly down-regulated in the WT group (P<0.05), while the luciferase activity was not significantly changed in the MUT group (P>0.05). In the over-expression experiment, compared with the H/R group, the cell apoptosis and the ratio of Bax/Bcl-2 were significantly reduced in the miR-873 mimic group (both P<0.05). Compared with miR-873 mimic group, the cell apoptosis and the ratio of Bax/Bcl-2 were significantly up-regulated in the H/R+pcEgln3 group and the H/R+miR-873 mimic+pcEgln3 group (all P<0.05). Conclusion: MiR-873 can inhibit H/R- induced apoptosis of cardiomyocyte via targeting Egln3.
响应面法优化芦荟中抗氧化活性成分的提取工艺_唐远谋
第9卷第1期2011年1月生 物 加 工 过 程Ch i nese Journa l o f B ioprocess Eng i neer i ng V o.l 9N o .1Jan .2011do:i 10.3969/.j issn .1672-3678.2011.01.006收稿日期:2010-07-14作者简介:唐远谋(1986 ),男,四川南充人,硕士研究生,研究方向:食品营养与安全;焦士蓉(联系人),副教授,硕士生导师,E-m ai:lj s -rong2004@163.co m响应面法优化芦荟中抗氧化活性成分的提取工艺唐远谋1,焦士蓉1,冷 鹂2,唐鹏程1,刘 佳1,冯 慧1(1.西华大学生物工程学院,成都610039;2.四川大学生命科学学院,成都610064)摘 要:对芦荟中抗氧化活性物质提取工艺及其成分进行研究,通过单因素实验和响应面优化,以提取物对DPPH 自由基的清除率为抗氧化的考察指标,得到芦荟中抗氧化活性成分的提取工艺条件:提取温度29 、料液比(g /mL)1 33、提取时间107s 、微波功率500W,微波辅助水提,此条件下得到的提取物对DPPH 自由基的清除率达91 414%。
提取物活性成分分析表明:提取物中芦荟甙含量为1 5m g /g 、黄酮为1 13mg /g 、多酚为4 33m g /g 、多糖为126 36mg /g 。
关键词:芦荟;抗氧化物质;DPPH 自由基;提取;响应曲面法中图分类号:TS201.1 文献标志码:A 文章编号:1672-3678(2011)01-0024-05Opti m izati on of process para m eters of extraction antioxi dantsfro m A loe usi ng response surface m ethodol ogyTANG Yuan m ou 1,JI A O Sh irong 1,LENG L i 2,TANG Pengcheng 1,LI U Jia 1,FENG Hu i1(1.Schoo l o f B i oeng i neer i ng,X i hua U niversity ,Chengdu 610039,China ;2.Schoo l o f L ife Sc i ences ,Sichuan U ni v ers it y ,Chengdu 610064,Chi na)Abst ract :The process para m eters for extraction o f antiox i d ants fro m Aloe w ere opti m ized and the co m po -nents w ere analyzed .The opti m al process conditi o ns w ere attained by sing le factor m ethod and response surface m e t h odogy .Anti o x idant ab ilicy w as evalvated on the scaveng ing rate o fDPP H free radica.l M icro -w ave assisted ex traction(MAE )by w ater w as chosed and t h e solid -li q u i d ratio w as 1 33,m icro w ave po w -er w as 500W at 29 for 107s .Under t h ese conditi o ns ,the re m ova l rate of DPP H w as 91 414%.The resu lts o f co m ponent analysis for antiox idants show ed that the y ie l d of a l o in ,flavono i d s ,po l y pheno ls ,and po l y sacchari d e w ere 1 5m g /g ,1 13m g /g ,4 33m g /g ,and 126 36m g /g ,respectively .K ey w ords :A loe ;anti o x i d ants ;DPP H free rad ica;l extracti o n ;response surface m ethod 芦荟系百合科(L iliaceae )芦荟属(A loe )多年生的常绿、肉质草本植物,原产于非洲[1]。
microRNA-182抑制人角膜上皮细胞增殖和迁移
·论著·Original Article·
microRNA-182抑制人角膜上皮细胞增殖 和迁移
曹琼洁 赵晓婷 敬霞 王教 陈晓燕 闫东升 瞿佳
摘要 目的:通过体内动物实验与体外细胞实验来阐明microRNA-182(miR-182)在角膜上皮损伤修复中的 功能。方法:实验研究。体内实验选取5 只C57BL/6J野生型小鼠,通过机械刮伤法构建小鼠角膜上 皮损伤修复模型作为实验组,对侧眼作为对照组,通过实时定量RT-PCR法检测miR-182 在损伤修复 过程(损伤后48 h)的表达。体外实验采用脂质体介导的方法将miR-182 和随机序列寡核苷酸链转染 入人角膜上皮细胞(HCECs),通过细胞增殖实验(MTS法)和细胞克隆形成实验检测细胞增殖和生 长能力,流式细胞术检测细胞周期,细胞划痕实验检测细胞迁移能力。MiR-182 表达量及细胞实验 各参数 2 组间比较采用独立样本t检验。结果:体内实验中,与对照组相比,实验组中 5 个样本量的 miR-182 在角膜上皮损伤修复过程中表达水平显著下调(t=147.6、79.2、136.8、41.3、89.8,均 P<0.001)。体外实验中,miR-182组相对细胞数目为(81±5)%,与阴性对照组(100%)相比显著减少(t=6.6, P=0.003),同时miR-182组细胞克隆数明显少于阴性对照组。细胞周期检测结果显示实验组处于G1期细 胞数量比例为(49±7)%,明显高于阴性对照组的(35±4)%(t=-3.0,P=0.041)。此外,细胞迁移实验 结果显示miR-182组HCECs细胞迁移的距离为(99±12)μm,而阴性对照组的迁移距离为(213±14)μm (t=10.8,P=0.001),迁移速度明显变慢。结论:miR-182 通过抑制角膜上皮细胞的增殖与迁移,从而对 角膜上皮损伤修复起到负调控的作用。 关键词:角膜损伤修复;miR-182;角膜上皮细胞;增殖;迁移 基金项目:温州市科技计划项目(Y20160188)
Invasive and indigenous microbiota impact intestinal stem cell
10.1101/gad.1827009Access the most recent version at doi: 2009 23: 2333-2344Genes Dev.Nicolas Buchon, Nichole A. Broderick, Sveta Chakrabarti, et al.Drosophilaactivity through multiple pathways in Invasive and indigenous microbiota impact intestinal stem cellMaterial Supplemental/content/suppl/2009/10/02/23.19.2333.DC1.html References/content/23/19/2333.full.html#related-urls Article cited in:/content/23/19/2333.full.html#ref-list-1This article cites 39 articles, 8 of which can be accessed free at:Related ContentGenes Dev. October 1, 2009 23: 2260-2265Won-Jae Leehomeostasis Bacterial-modulated host immunity and stem cell activation for gut serviceEmail alertingclick here top right corner of the article or Receive free email alerts when new articles cite this article - sign up in the box at the/subscriptions go to: Genes & Development To subscribe to Copyright © 2009 by Cold Spring Harbor Laboratory PressInvasive and indigenous microbiota impact intestinal stem cell activity through multiple pathways in DrosophilaNicolas Buchon,2Nichole A.Broderick,Sveta Chakrabarti,and Bruno Lemaitre1Global Health Institute,Ecole Polytechnique Federale de Lausanne(EPFL),CH-1015Lausanne,SwitzerlandGut homeostasis is controlled by both immune and developmental mechanisms,and its disruption can lead to inflammatory disorders or cancerous lesions of the intestine.While the impact of bacteria on the mucosal immune system is beginning to be precisely understood,little is known about the effects of bacteria on gut epithelium renewal.Here,we addressed how both infectious and indigenous bacteria modulate stem cell activity in Drosophila.We show that the increased epithelium renewal observed upon some bacterial infections isa consequence of the oxidative burst,a major defense of the Drosophila gut.Additionally,we provide evidence that the JAK–STAT(Janus kinase–signal transducers and activators of transcription)and JNK(c-Jun NH2terminal kinase)pathways are both required for bacteria-induced stem cell proliferation.Similarly,we demonstrate that indigenous gut microbiota activate the same,albeit reduced,program at basal levels.Altered control of gut microbiota in immune-deficient or aged flies correlates with increased epithelium renewal.Finally,we show that epithelium renewal is an essential component of Drosophila defense against oral bacterial infection.Altogether, these results indicate that gut homeostasis is achieved by a complex interregulation of the immune response,gut microbiota,and stem cell activity.[Keywords:Intestinal stem cell;proliferation;gut microbiota;JAK–STAT;JNK;pathogenic bacteria] Supplemental material is available at .Received June2,2009;revised version accepted August25,2009.The gut of all organisms is in constant exposure to en-vironmental and microbial aggressions(Sansonetti2004). It is an active barrier,limiting invasion by pathogenic microorganisms and promoting tolerance to indigenous microbiota(Pedron and Sansonetti2008).To maintain homeostasis,the gut epithelium is constantly renewed throughout an organism’s life by the division and differ-entiation of intestinal stem cells(ISCs).In Drosophila, ISCs are scattered along the basement membrane of the midgut(Micchelli and Perrimon2006;Ohlstein and Spradling2006).The division of an ISC generates both a new ISC and a post-mitotic enteroblast,which differ-entiates into either an absorptive enterocyte or a secre-tory enteroendocrine cell.In basal conditions,the adult gut epithelium is renewed in;1–2wk(Micchelli and Perrimon2006).We recently reported a global analysis of the changes in gene expression that occur in the Drosophila gut in response to infection by a Gram-negative bacterium, Erwinia carotovora carotovora15(Ecc15)(Buchon et al. 2009).This study demonstrated that bacterial infec-tion triggers expression of a combination of immune, stress,and developmental signaling pathways.Most im-mune genes—notably,antibacterial peptide genes(e.g., Diptericin)—are induced in the gut by the Imd pathway. This pathway is activated upon recognition of peptido-glycan of Gram-negative bacteria by the transmembrane receptor PGRP-LC,and leads to activation of the NF-k B protein Relish(Zaidman-Remy et al.2006).Subsequent analysis showed that the JAK–STAT(Janus kinase–signal transducers and activators of transcription)signaling pathway was activated by damage in the gut of infected flies and regulates the production of a subset of antimi-crobial peptides.Surprisingly,it was further observed that ingestion of Ecc15strongly stimulates ISC division,pro-moting a rapid turnover of the gut epithelium(Buchon et al.2009).These results highlighted an unexpected link between oral bacterial infection and epithelial renewal. These data also suggested that,following infection,gut homeostasis is maintained by the balance between cell damage induced by infection and epithelial repair by ISC activation.However,the precise causes of ISC prolifera-tion,as well as the signaling events regulating this induction,were unclear,as was the effect of indigenous or lethal bacteria on this mechanism.Here we use the genetically tractable model Drosophila melanogaster to study the link between gut bacteria,theCorresponding authors.1E-MAIL bruno.lemaitre@epfl.ch;FAX41-21-693-17-90.2E-MAIL nicolas.buchon@epfl.ch;FAX41-21-693-17-90.Article is online at /cgi/doi/10.1101/gad.1827009.GENES&DEVELOPMENT23:2333–2344Ó2009by Cold Spring Harbor Laboratory Press ISSN0890-9369/09;2333gut immune response,and epithelium renewal.We show that the oxidative burst,induced by the host consecutive to Ecc15infection,is a major inducer of ISC activation. Infection with this bacterium activates both JAK–STAT and JNK(c-Jun NH2terminal kinase)pathways in ISCs to promote proliferation.Indigenous bacteria induce the same program and lead to a basal level of proliferation. Inversely,Pseudomonas entomophila,a lethal entomo-pathogenic bacterium,interferes with ISC activation, thereby disrupting gut homeostasis.ResultsInfection-induced oxidative burst is a major inducerof epithelium renewalThe gut immune response of Drosophila has two main components:an initial oxidative burst by the NADPH oxidase enzyme Duox(Ha et al.2005a),followed by the synthesis of antimicrobial peptides controlled by the Imd pathway.Previously,we reported that oral infection with Ecc15stimulates epithelium turnover in the intestine and strongly activates the transcription of genes known to respond to oxidative stress(Buchon et al.2009).Since Ecc15is known to induce Duox activity(Ha et al.2005a), we hypothesized that the oxidative burst induced upon ingestion of Ecc15could be a major inducer of both gut damage and epithelium renewal.To test this,we moni-tored epithelium renewal following ingestion of Ecc15in flies in which the level of reactive oxygen species(ROS) had been artificially reduced.Intestinal epithelium re-newal can be monitored easily in Drosophila by(1) counting the number of dividing cells along the midgut using an anti-phosphohistone H3(anti-PH3)antibody as an indicator of mitotic activity;(2)using the esgGal4, UAS-GFP marker,which strongly labels ISCs,entero-blasts,and newly synthesized enterocytes;or(3)by cell lineage analysis revealing the expansion of lacZ-marked clones;with the two latter monitoring not only cell division,but also epithelium differentiation(Micchelli and Perrimon2006;Ohlstein and Spradling2006).As shown previously,we detected a massive epithelium renewal following ingestion of Ecc15by both clonal analysis and the stem cell marker esgGal4,UAS-GFP. In contrast,epithelium renewal did not increase in flies fed Ecc15in combination with the antioxidants N-acetyl cysteine(NAC)or glutathione(Fig.1A,B;quantification in Supplemental Fig.S1C),although these two com-pounds did not affect Ecc15viability(Supplemental Fig. S1A,B).Conversely,ingestion of paraquat,a potent in-ducer of ROS,induced epithelium renewal without in-fection(Fig.1A,B),in agreement with previous studies (Biteau et al.2008;Buchon et al.2009;Chatterjee and Ip 2009).While increased ISC proliferation was observed in Imd-deficient flies infected orally with Ecc15(Buchon et al. 2009),silencing of the Duox gene by RNAi significantly reduced the number of mitotic ISCs detected with anti-PH3(Fig.1C).Similarly,ISC proliferation was also re-duced in flies carrying either a mutation in G a q,which Figure 1.Immune-stimulated oxidative burst induces stem cell activation in the gut.(A)Large lacZ-marked clones con-taining the tubulin promoter-lacZ fusion due to mitotic re-combination are observed in the guts of flies orally infected with Ecc15or fed with paraquat.No expansion of lacZ clones was detected in the gut of flies fed with both Ecc15and antioxidants (NAC or gluthathione).Quantification of lacZ clones is shown in Supplemental Figure S1C.(B)Ingestion of Ecc15or paraquat induces a marked increase in the number of esgGal4,UAS-GFP-positive cells.In contrast,coingestion of Ecc15and glutathione did not induce epithelium renewal.In unchallenged flies,most of the GFP signal corresponds to ISCs.In Ecc15-infected flies, the GFP signal was observed in both ISCs and ISC-derived daughter cells(see Supplemental Fig.S6for distribution of escargot-positive cells along the midgut).Flies were collected 16h post-infection.(C)Quantification of PH3-positive cells per midgut of unchallenged(UC)flies or flies collected4h after feeding with Ecc15,paraquat,or H2O2.Guts of Duox RNAi flies (daGal4,UAS-Duox-IR),G a q-deficient flies,or flies overex-pressing a catalase(daGal4,UAS-IRC)orally infected with Ecc15exhibit a lower number of dividing ISCs compared with wild type.Mean6standard deviation(SD)are shown.Values significantly different in a Student’s t-test(P<0.001)are denoted by three asterisks(***).Buchon et al.2334GENES&DEVELOPMENTencodes a heterodimeric G protein responsible for Duox enzymatic activation(Ha et al.2009),or overexpressing IRC,a catalase involved in ROS detoxification(Fig.1C; Ha et al.2005b).Collectively,our results indicate that the increased epithelium renewal observed upon infection with Ecc15is largely a consequence of the oxidative burst resulting from Duox activation in response to infection. Reduced ISC proliferation in flies with reduced Duox activity or coinfected with Ecc15and antioxidants was correlated with reduced levels of cell death in the gut (data not shown).This suggests that the increase in epithelium renewal is not a direct effect of ROS,but rather an effect of the damage caused by the oxidative burst.In agreement with this,the ingestion of toxic compounds such as SDS,DSS,or bleomycin is sufficient to induce epithelium renewal(Amcheslavsky et al.2009; Buchon et al.2009).Activation of the JAK–STAT pathway in ISCsby the cytokine Upd3stimulates epitheliumrenewal upon Ecc15infectionWe next investigated the nature of the signaling pathways stimulating epithelium renewal upon Ecc15infection. The JAK–STAT pathway has been implicated in stem cell control in Malpighian tubules,testis,and ovaries (Gregory et al.2008).We demonstrated previously that three genes encoding components of the JAK–STAT pathway—the receptor Domeless;one of its ligands,Un-paired3(Upd3);and a repressor of the receptor/JAK complex,Socs36E—were strongly induced in the gut following ingestion of Ecc15and paraquat(Buchon et al. 2009).Interestingly,the level of JAK–STAT signaling activity in Ecc15-infected guts was reduced in Duox RNAi flies or flies fed with antioxidants,as revealed by the decreased induction of the target genes upd3and Socs36E,and of the JAK–STAT reporter gene STAT-GFP (Fig.2A;Bach et al.2007;data not shown).Moreover,use of the STAT-GFP reporter gene revealed that the JAK–STAT pathway is already active at a basal level in ISCs and enteroblasts of unchallenged flies(Supplemental Fig.S2A). The strong correlation between stimuli activating stem cell proliferation and those inducing JAK–STAT activity prompted us to examine the role of the JAK–STAT pathway in controlling ISC proliferation upon bacterial infection. In this aim,we expressed RNAi or dominant-negative constructs targeting JAK–STAT pathway components in either ISCs(using esgGal4)or enterocytes(using NP1Gal4)and monitored stem cell activity.Stem cell proliferation in the midgut,as monitored by the number of PH3-positive cells,was still observed in flies with reduced STAT activity in enterocytes(NP1Gal4,UAS-STAT92E-IR)(Fig.2B).The mitotic index was even higher than in wild-type flies.Since the expression of a STAT92E-IR construct driven by esgGal4resulted in lethality,we generated conditional STAT92E-IR individ-uals by combining the esgGal4transgene and a thermo-sensitive version of the Gal4inhibitor,tubGal80TS(re-ferred to as esgGal4TS).When reared at a restrictive temperature(18°C,Gal80TS on,Gal4system off)during their entire development,adult flies displayed a wild-type number and distribution of ISCs.However,shifting flies to a permissive temperature(29°C,Gal80TS off,Gal4 system on)for3d to deplete STAT in ISCs changed the pattern of escargot-positive cells along the midgut(Fig. 2C;Supplemental Fig.S2B).In the anterior midgut,we observed a reduction in the number of escargot GFP-positive cells.However,small aggregates of escargot GFP-positive cells were observed occasionally in the anterior midgut of esgGal4TS STAT92E-IR flies(indicated by an arrow in Fig.2C3).In contrast,a high number of GFP-positive cells were consistently observed in the posterior region of the midgut.These cells were small-nucleated and did not express the ISC marker Delta or the enteroendo-crine marker Prospero,raising the possibility that they are enteroblasts(Supplemental Fig.S2C,D).This suggests that the JAK–STAT pathway is not required for ISC prolifera-tion,but rather for the proper differentiation of ISC prog-eny in basal turnover conditions.In contrast to wild-type flies,no increase in the number of mitotic cells(PH3-positive)nor change in the pattern and distribution of escargot GFP-positive cells was observed in the gut of esgGal4TS STAT92E-IR flies upon Ecc15infection(Fig. 2B,C),indicating a lack of epithelium renewal induction. Similar results were obtained with the use of the domi-nant-negative version of the JAK–STAT pathway receptor Domeless(Fig.2B;Brown et al.2001;data not shown). We further tested the effect of reducing JAK–STAT signaling by generating mosaic animals with clones that are mutant for the STAT92E transcription factor(Lee and Luo2001;Krezmien et al.2007).Upon Ecc15infection of the mosaic flies,STAT92E mutant clones were rarely observed,but when present were composed of only small-nucleated cells.In contrast,control clones contained both small diploid progenitors and large polyploid entero-cytes(Supplemental Fig.S2E).This indicates that a re-duction in JAK–STAT signaling in ISCs blocks epithelium renewal induced upon Ecc15infection.Finally,overex-pressing a gain-of-function form of the JAK kinase Hop in ISCs(UAS-hop Tum)triggered epithelium renewal without infection(Fig.2B,D1).We conclude that the JAK–STAT pathway is required in ISCs for the increased epithelium renewal induced upon bacterial infection with Ecc15. We reported previously that the JAK–STAT ligand upd3 is transcriptionally induced in the gut upon ingestion of both Ecc15and paraquat(Buchon et al.2009).Use of an upd3-Gal4;UAS-GFP reporter transgene(Agaisse et al. 2003)revealed that upd3was expressed mostly in entero-cytes(Fig.2E).In agreement,upd3expression was decreased in flies when upd3-IR was expressed in entero-cytes,but not when it was expressed in ISCs(Supple-mental Fig.S2F).Interestingly,physical injury of the gut with forceps rapidly induced a localized expression of upd3(Fig.2F),demonstrating that Upd3is induced in the vicinity of damaged enterocytes and supporting its role in the activation of the JAK–STAT pathway in ISCs.Ac-cordingly,specific silencing of upd3expression in entero-cytes,but not in ISCs,strongly decreased the number of proliferative ISCs in response to infection(Fig.2B). Conversely,the ectopic expression of upd3in ISCs wasGut microbes and stem cell proliferationGENES&DEVELOPMENT2335sufficient to induce a high level of epithelium renewal in the absence of infection (Fig.2D2).Altogether,these results indicate that upon Ecc15infection,enterocytes release Upd3,which activates the JAK–STAT pathway in ISCs to promote proliferation and to repair damage to the gut.The JNK pathway is required for ISC maintenance and proliferation in the gut of infected fliesThe JNK pathway is activated by a variety of environ-mental challenges,including oxidative stress,and was demonstrated recently to be required in ISCs to maintain gut homeostasis in aging flies (Wang et al.2003;Biteau et al.2008).We reported previously that the JNK pathway is activated in the gut of flies soon after ingestion of Ecc15(Buchon et al.2009).Furthermore,coimmunostaining of the ISC marker esg-GFP and of puckered (puc-lacZ ),a reporter of JNK pathway activity (Martı´n-Blanco et al.1998),revealed that the JNK pathway was strongly activated in both enterocytes and ISCs upon Ecc15in-fection (Fig.3A).Interestingly,RT-qPCR analysis re-vealed that JNK induction was dampened in bothDuoxFigure 2.The JAK–STAT pathway is required for ISC proliferation upon Ecc15infection.(A )Oxidative stress modulates the activation of JAK–STAT and JNK pathways upon Ecc15infection.RT-qPCR analysis of gut extracts shows that the expression levels of JAK–STAT (upd3,Socs36E ,monitored 4h post-infection)and JNK (puckered ,monitored 30min post-infection)target genes were reduced upon Ecc15infection in the gut of Duox RNAi flies or flies expressing a catalase (daGal4;UAS -IRC ).Ingestion of paraquat was sufficient to induce upd3,Socs36E ,or puckered .In contrast,the level of Diptericin (a gene tightly regulated by the Imd pathway)was not affected by conditions modulating ROS.Mean of four independent experiments 6SD are shown.(B )Quantification of PH3-positive cells per midgut shows an increase in the number of mitotic cells upon Ecc15infection in both wild-type flies and flies with reduced JAK–STAT activity in enterocytes (NP1Gal4,UAS-STAT92E-IR ),but not in ISCs (esgGal4TS ,UAS-STAT92E-IR ).Silencing of upd3in enterocytes (NP1Gal4,UAS-upd3-IR ),but not in ISCs (esgGal4,UAS-upd3-IR ),reduced the number of mitotic ISCs in the guts of flies collected 4h after feeding with Ecc15.Overexpression of a gain-of-function allele of hop in ISCs increases the mitotic index (esgGal4TS ,UAS-hop Tum ).Mean 6SD are shown.Values significantly different from infected wild-type flies in a t -test at P <0.001are denoted by three asterisks (***).(C1–C5)A loss of stem cells was observed in the anterior region of esgGal4TS ,UAS-STAT92E-IR flies raised at 29°C.In some flies,accumulation of small-nucleated escargot-positive cells were observed in the anterior part of the midgut,as indicated with a red arrow in C3.(C4)Accumulation of small-nucleated escargot-positive cells was observed in the posterior regions of the gut of all esgGal4TS ,UAS-STAT92E-IR flies raised at 29°C,in the absence of infection.(C5)No increase in epithelium renewal was observed in these flies upon infection with Ecc15,as indicated by the lack of large nuclei cells expressing GFP.Expression of the esgGal4,UAS-GFP reporter gene was monitored 16h after infection with Ecc15.(D1,D2)Overexpression of hop Tum (D1)or upd3(D2)in ISCs is sufficient to induce a high level of epithelium renewal in the absence of infection.(E )upd3expression is induced along the gut following Ecc15ingestion.(E1)upd3was expressed mostly in enterocytes 4h after Ecc15infection,as revealed by the GFP signal (green)of upd3Gal4UAS-GFP flies.(F )Physical damage to the gut with tweezers induced local expression of the upd3Gal4,UAS-GFP reporter within 30min following injury.Buchon et al.2336GENES &DEVELOPMENTRNAi flies and flies coinfected with Ecc15and anti-oxidants,as monitored by a decrease in expression of puckered,a target gene of the JNK pathway (Fig.2A).These results prompted us to investigate the involvement of the JNK pathway in ISC proliferation during bacterial infection.Silencing the transcription factor dJun in ISCsby RNAi resulted in the loss of ISCs along the gut of unchallenged flies,as indicated by the absence of escargot GFP-positive cells (Fig.3B).Immunostaining with the ISC-specific marker Delta confirmed that the absence of esgargot GFP-positive cells corresponded with the loss of ISCs (data not shown).Similar results were obtained when the inducible esg-Gal4tubGAL80ts system was used to drive the dJun-IR construct,indicating that the loss of ISCs does not result from an effect of JNK during development (data not shown).Interestingly,knockdown of the JNK basket or the JNK kinase (JNKK)hemipterous (hep )in ISCs or overexpression of a negative regulator of JNK signaling (UAS-puckered )did not alter the number of ISCs in unchallenged flies (Fig.3B;data not shown).However,upon Ecc15infection,the number of ISCs was decreased dramatically in the gut of flies with reduced JNK activity,and no epithelium renewal was observed (Fig.3B).Moreover,immunostaining for the apoptotic marker caspase3revealed that,upon Ecc15infection,some remaining ISCs were undergoing apoptosis when depleted for the JNK Basket (Supplemental Fig.S3A).Importantly,no increase in the number of dividing cells was observed upon Ecc15infection in the gut of flies with reduced JNK activity in ISCs,as monitored by the number of PH3-positive cells (Supplemental Fig.S3B).In contrast,overexpression of hep with the esg-Gal4TS driver led to increased epithelium renewal in the absence of infection (Fig.3B;Supplemental Fig.S3B).We conclude that the lack of JNK pathway activity in ISCs results in a premature loss of ISCs and the conse-quent absence of epithelium renewal upon bacterial infection with Ecc15.Epithelium renewal is an essential component of Drosophila defense to Ecc15Both wild-type and Imd-deficient flies survive ingestion of Ecc15(Basset et al.2000),indicating that even without a functional Imd-dependent immune response,this bac-terium is not lethal.Importantly,we observed no differ-ence in the level of epithelium renewal between wild-type and Imd-deficient flies in response to Ecc15(Buchon et al.2009).In contrast,reduction of JNK or JAK–STAT signaling in ISCs abolishes the epithelium renewal that is induced upon infection with Ecc15,but does not affect the Imd-dependent immune response (data not shown).To analyze the extent to which epithelium renewal is important in the resistance to Ecc15infection,we com-pared the survival of flies in which the activity of the JNK (UAS-basket-IR ,UAS-dJun-IR ),JAK–STAT (UAS-upd3-IR or UAS-STAT92E-IR ),and Imd (UAS-dFadd-IR )path-ways had been selectively reduced in either enterocytes (Fig.4A)or ISCs (Fig.4B).Strikingly,flies impaired in their capacity to renew their epithelium—due to the inhibition of either JAK–STAT or JNK signaling in ISCs,or the silencing of upd3in enterocytes—succumbed 4–8d following ingestion of Ecc15(Fig.4A,B).Examination of flies impaired in epithelium renewal at 4d revealed that their guts were morphologically altered,with regions devoid of enterocytes (Fig.4C)or displaying aberrantcellFigure 3.The JNK pathway is required for ISC maintenance and proliferation upon Ecc15infection.(A )Immunostaining with antibodies against GFP (red)or LacZ (green)of esgGal4,UAS-GFP,puc E69(puc-lacZ )flies collected 30min after Ecc15infection shows that the level of JNK signaling activity in-creases (top center panel,compared with middle center panel)upon Ecc15infection in both enterocytes and ISCs,the staining being more intense in ISCs (merge,right panels);higher magni-fication is shown in the bottom panels.(B )Loss of ISCs and the absence of epithelium renewal were observed in the guts of flies with reduced JNK activity in ISCs.Guts of flies carrying the esgGal4,UAS-GFP combined with UAS-dJun-IR ,UAS-basket IR ,or UAS-hep-IR were examined 16h post-infection with Ecc15.Silencing of dJun-IR in ISCs reduced the number of ISC in both unchallenged and challenged animals.In contrast,silencing of the genes encoding the JNK Basket and JNKK Hep in ISCs leads to a loss of ISCs only after infection with Ecc15.Ectopic expression of UAS-hep in ISCs induces epithelium renewal in the absence of infection.Gut microbes and stem cell proliferationGENES &DEVELOPMENT 2337shapes,suggesting a disruption in the continuity of the gut and a lack of tissue integrity.The corresponding increase in susceptibility demonstrates that epithelium renewal is necessary for the proper recovery of flies after infection with Ecc15and is more critical than the Imd pathway in the response to this bacterium.Indigenous microbiota impact epithelium renewal through ISC stimulationEven in basal conditions,the gut is permanently in contact with indigenous microorganisms (Hooper 2004).We used axenically raised flies to investigate how gut microbiota impact epithelium renewal.Both the number of mitotic ISCs and the rate of epithelium renewal were reduced in axenic flies as compared with conventionally raised (CR)flies (Fig.5A;Supplemental Fig.S4A,B).This reduction in epithelium renewal was not due to an inability of axenic flies to activate renewal,as infection with Ecc15and reintroduction of culturable indigenous bacteria increased mitotic activity in these flies (data not shown).Moreover,RT-qPCR analysis demonstrated thatthe gut microbiota regulate,to some extent,the basal levels of JAK–STAT,JNK,and Imd pathways (Fig.5B).Use of the upd3Gal4,UAS-GFP reporter gene revealed that upd3was expressed at low levels in a few cells scattered along the gut of CR flies.In sharp contrast,no expression of upd3was observed in the gut of axenic flies (Fig.5C).Taken together,these data suggest that,under normal conditions,gut microbiota stimulate these pathways,promoting a basal level of epithelium renewal.Interest-ingly,higher numbers of dividing cells were detected in the absence of infection in the guts of Relish E20or PGRP-LC E12flies,which are deficient for the Imd pathway (Fig.5A).These flies harbor 10-fold higher counts of indige-nous bacteria than wild-type (Supplemental Fig.S4C),suggesting that an abnormally abundant microbiota could increase epithelium renewal.To test this hypoth-esis,we raised Relish E20and PGRP-LC E12flies in axenic conditions and monitored ISC proliferation by anti-PH3staining.Increased ISC proliferation was no longer ob-served in Relish E20and PGRP-LC E12axenic flies (Fig.5A).These data indicate that indigenous bacteria condition the basal level of epithelium renewal by stimulating ISC division,probably through an increase of JAK–STAT and JNK activity.Recent studies have revealed that age-related deterio-ration of the intestinal epithelium is associated with excessive ISC proliferation and aberrant differentiation (Biteau et al.2008;YJ Choi et al.2008;Park et al.2009).In agreement with this,we observed a 10-fold higher mitotic index in the midguts of 30-d-old flies as compared with 3-d-old flies by anti-PH3staining (Fig.5A).Moreover,increased esgGal4,UAS-GFP signal was observed in the guts of 30-d-old flies (Fig.5D1),at a similar level to that observed with Ecc15infection.Higher magnification revealed the accumulation of large,rounded escargot-positive cells,described previously as a hallmark of gut disorganization upon aging (Fig.5D2;Biteau et al.2008).This deregulation of epithelium renewal correlated with increased expression levels of target genes of the JNK,JAK–STAT,and Imd pathways (Fig.5B).These age-dependant symptoms were exacerbated in the Relish E20flies (Fig.5A),whose guts were morphologically al-tered with regions devoid of enterocytes (Supplemental Fig.S4D).Interestingly,guts from both wild-type and Relish E2030-d-old flies contain higher counts of indige-nous bacteria than their younger counterparts (Supple-mental Fig.S4C;Ren et al.2007),raising the possibility that the increased epithelium renewal in older flies could be caused by the abundant microbiota.We examined axe-nically raised flies to investigate how gut microbiota im-pact age degeneration of the gut.Strikingly,guts from 30-d-old flies raised axenically have levels of epithelium renewal more similar to that of young flies,as indicated by the mitotic index and use of the esgGal4,UAS-GFP marker (Fig.5A,D).This correlates with reduced levels of JNK and JAK–STAT activity (Fig.5B).Moreover,the guts of old Relish E20axenic flies do not exhibit alterations in intestinal integrity (Supplemental Fig.S4D).These data indicate that age-related defects in the gut are largely reverted in the absence of indigenousbacteria.Figure 4.Epithelium renewal is required for proper resistance to Ecc15infection.(A ,B )Survival analysis at 29°C shows that flies impaired in epithelium renewal succumbed 4–8d follow-ing ingestion of Ecc15.UAS-dFADD-IR ,UAS-basket-IR ,UAS-dJun-IR ,or UAS-upd3-IR constructs were expressed in either enterocytes (NP1Gal4;A )or ISCs (esgGal4or esgGal4TS ;B ).(C )Guts of flies impaired in epithelium renewal displayed altered gut morphology as revealed by the lack of DAPI nuclear staining.Flies were observed 4d post-infection.Buchon et al.2338GENES &DEVELOPMENT。
不同温度下飞秒激光制备的微纳结构表面对撞击液滴运动行为的影响
Applied Physics 应用物理, 2020, 10(2), 161-167Published Online February 2020 in Hans. /journal/apphttps:///10.12677/app.2020.102020Effect of Surfaces of Micro-Nano StructuresPrepared by Femtosecond Lasers onMotion of Impacting Droplets atDifferent TemperaturesJia Guo1, Lei Xue2, Haiyan Tao1*1Ultrafast Optics Laboratory, Changchun University of Science and Technology, Changchun Jilin2Chengdu Kaitian Electronics Co., Ltd., Avionics Research Institute, Chengdu SichuanReceived: Feb. 5th, 2020; accepted: Feb. 20th, 2020; published: Feb. 27th, 2020AbstractThe phenomenon of droplets hitting a solid surface is of great significance for technical fields such as ice protection, heat transfer and water management. Unlike normal and low temperature conditions, when the solid surface temperature rises to a certain range, the droplets hitting the surface will be ina thermal state called Leidenfrost, at which time the droplets will become quite active. In this state,analyzing the motion behavior of the impacting droplets is very challenging. In this paper, we pre-pared micro-nano structured surfaces with different morphologies by using femtosecond laser processing technology. By comparing the impact behavior of droplets of two types of ultra-wettable and ultra-hydrophobic surfaces with different wettability at different temperatures, we analyzed the influence of temperature on the motion of droplets hitting the surface. This research is of great sig-nificance for understanding and controlling droplet dynamics, and opens up new ideas for the ap-plication of high temperature multifunctional surfaces in the future.KeywordsFemtosecond Laser, Micro-Nano Morphology, High Temperature Environment, Leidenfrost State, Impact Droplet不同温度下飞秒激光制备的微纳结构表面对撞击液滴运动行为的影响郭嘉1,薛磊2,陶海岩1**通讯作者。
模拟微重力下瘦素对肺T淋巴细胞蛋白激酶C信号转导途径的影响
模拟微重力下瘦素对肺T淋巴细胞蛋白激酶C信号转导途径的影响李旭;刘长庭【期刊名称】《中国药物与临床》【年(卷),期】2014(000)005【摘要】Objective To investigate the effects of leptin on protein kinase C (PKC) of pulmonary T lympho-cytes under a simulated microgravity. Methods Lung T lymphocytes isolated from rats were cultured by using rotary cell culture system (RCCS) technology which simulated microgravity. Following incubation of T lymphocytes, the cel-lular PKC activity of T lymphocytes was determined by using PepTag′s non-radioactive PKC assay kit. The level of IL-2 was measured by enzyme-linked immunosorbent assay kits (double-antibody). And flow cytometry was applied to measure the expression of surface antigen CD25 and CD71. Results In the normal gravity environment, the PKC ac-tivity, IL-2 production, the activation of cellular surface CD25 were increased when ConA group compared with leptin group and ConA+leptin group compared with ConA group (bothP<0.01). Exposure to microgravity conditions, when compared with normal gravity group, resulted in attenuated PKC activity, IL-2 production and the activation of cellular surface CD25 in ConA group (all P<0.01). However, the differences in PKC activity, IL-2 production and the activa-tion of cellular surface CD25 were unremarkable among leptin group, ConA groupand ConA+leptin group (all P>0.05) when exposed to microgravity conditions. Compared with normal gravity, the RCCS was associated with significantly lower levels of the aforementioned parameter in ConA+leptin group (all P<0.01). When to microgravity conditions, lep-tin group and ConA+leptin group were associated with lower levels of the aforementioned parameters as compared with ConA+PMA group (allP<0.01). Conclusion Exposure to microgravity conditions accounts for inhibited T lympho-cyte activation, attenuated PKC activity , reduced number of CD25 expressing cells and IL-2 production, which could be restored by PMA.%目的:探讨在模拟微重力下瘦素对肺T淋巴细胞蛋白激酶C (PKC)信号转导途径的影响。
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Technical NoteEffect of microencapsulated phase change material in sandwich panelsCecilia Castellón a ,Marc Medrano a ,Joan Roca a ,Luisa F.Cabeza a ,*,Maria E.Navarro b ,1,Ana I.Fernández b ,Ana Lázaro c ,2,Belen Zalba c ,2aGREA InnovacióConcurrent,Edi fici CREA,Universitat de Lleida,Pere de Cabrera s/n,25001Lleida,Spainb Departamento de Ciencias de los Materiales e Ingeniería Metalúrgica,Universitat de Barcelona,Martíi Franqués 1,08028Barcelona,Spain cInstituto de Investigación en Ingeniería de Aragón,I3A,Grupo de Ingeniería Térmica y Sistemas Energéticos (GITSE),Dpto.Ingeniería Mecánica,Área de Máquinas y Motores Térmicos,Universidad de Zaragoza,Campus Politécnico Río Ebro,Edi ficio “Agustín de Betancourt,”María de Luna s/n,50018Zaragoza,Spaina r t i c l e i n f oArticle history:Received 10December 2008Accepted 23March 2010Available online 24April 2010Keywords:Sandwich panelPhase change material (PCM)Thermal energy storage (TES)Microencapsulationa b s t r a c tSandwich panels are a good option as building materials,as they offer excellent characteristics in a modular system.The goal of this study was to demonstrate the feasibility of using the micro-encapsulated PCM (Micronal BASF)in sandwich panels to increase their thermal inertia and to reduce the energy demand of the final buildings.In this paper,to manufacture the sandwich panel with microencapsulated PCM three different methods were tested.In case 1,the PCM was added mixing the microencapsulated PCM with one of the components of the polyurethane.In the other two cases,the PCM was added either a step before (case 2)or a step after (case 3)to the addition of the polyurethane to the metal sheets.The results show that in case 1the effect of PCM was overlapped by a possible increase in thermal conductivity,but an increase of thermal inertia was found in case 3.In case 2,different results were obtained due to the poor distribution of the PCM.Some samples showed the effect of the PCM (higher thermal inertia),and other samples results were similar to the conventional sandwich panel.In both cases (2and 3),it is required to industrialize the process to improve the results.Ó2010Elsevier Ltd.All rights reserved.1.IntroductionNowadays,reduction of energy consumption is an important factor for existing buildings as well as for new buildings.Several extensive reviews and practical studies about this topic can be found in the literature [1e 5].These technical efforts concluded that it is necessary to develop materials and techniques to minimize the use of non-renewable energy for air conditioning purposes in buildings.Phase Change Materials (PCM)have been considered for thermal energy storage in buildings since 1980.Implementing the PCM in gypsum boards,plaster,concrete or other wall covering materials,thermal energy storage becomes a part of the building structure,useful even for light-weight buildings.In the literature,development and testing were conducted for prototypes of PCM wallboard and PCM concrete systems,with particular interest in peak load shifting and solar energy utilization.During the last 20years,new PCM products to be used in buildings appeared in the market.In these products,PCM ismacroencapsulated,having dif ficulties to be melted by direct solar radiation because of the poor heat conductivity of the PCM.On the other hand,the walls and ceilings of a building offer large areas for passive heat transfer within every zone of the building [5].Several researchers have investigated methods for impregnating gypsum wallboard and other architectural materials with PCM [1,6e 9].In these papers,different types of PCM and their characteristics are described.Other references discuss manufacturing techniques,thermal performance and applications of gypsum wallboard and concrete block,which have been impregnated with PCM [10e 12].Commercial buildings use sandwich panels as wall systems due to their excellent modular characteristics (Fig.1).These panels are mainly used in buildings,sport halls,and industrial buildings,giving them insulation properties not reached with other construction techniques.Sandwich panels integrate characteristics such as cladding,thermal insulation,water tightness,mechanical strength,and aesthetic appeal.It is a product composed of a ribbed sandwich panel formed by two metal sheets and insulating poly-urethane foam core injected in between.Some kinds of sandwich panel prototypes were studied,including air layer between the PCM (macroencapsulated in rigid containers)and the metal sheet.Results of the energetic behaviour were similar to high thermal mass walls [13].*Corresponding author.Tel.:þ34973003576;fax:þ34973003575.E-mail address:lcabeza@diei.udl.cat (L.F.Cabeza).1Tel.:þ34934021298;fax:þ349340335438.2Tel.:þ976762567;fax:þ976762616.Contents lists available at ScienceDirectRenewable Energyjournal ho me page:www.elsevier.co m/locate/renene0960-1481/$e see front matter Ó2010Elsevier Ltd.All rights reserved.doi:10.1016/j.renene.2010.03.030Renewable Energy 35(2010)2370e 2374The goal of this study was to demonstrate the feasibility of using a microencapsulated PCM (Micronal BASF)in sandwich panels to increase their thermal inertia and to reduce the energy demand of the final building.2.Experimental methodology with the sandwich panel The experimental methodology of this study was developed with the idea of including the PCM in sandwich panels,as well as,ful filling some technical requirements (standards)of the conven-tional sandwich panel that may be affected by the inclusion of PCM.Therefore,the speci fic objectives of this study are:to study different methods to include microencapsulated PCM;to demon-strate a higher thermal inertia in the sandwich panel by the inclusion of microencapsulated PCM without reducing its insu-lating properties.Other objectives are to obtain an homogeneous distribution of the microcapsules of PCM in the sandwich panel and to achieve the standard of adhesion for sandwich panels (such as UNE 41950).The conventional process of manufacturing sandwich panel is a continuous injection of an insulating polyurethane foam core between two metal sheets of galvanized pre-lacquered steel.For the addition of PCM,two manufacturing options were studied:Without modifying the standard manufacturing process,add-ing a mix of polyurethane and PCM (case 1).Modifying the manufacturing process,with the addition of a new step to include microencapsulated PCM.This new step may be done in two different ways (case 2or case 3).Case 1consists of mixing the microencapsulated PCM with one of the liquid components of the polyurethane.This process was tested with collaboration of PLASFI,and was studied only with the insulating polyurethane (without including the metal sheet).In case 2,the PCM was added at the beginning of the manufacturing process,just before the injection of the poly-urethane (Fig.2)and,in case 3,the PCM was added after the polyurethane (Fig.3).These experiments were performed in Europer fil.In these two last options,an 8%in weight of PCM with respect to the weight of the PUR was added manually,and samples from resulting PCM-sandwich panels were taken to evaluate how the microencapsulated PCM was distributed in the sandwich panel.For each case,a reference sample without PCM was also produced.Table 1shows the properties of the microencapsulated PCM used.The reference samples and samples with PCM were cut in smaller subsamples and the following tests were carried out: Distribution of the PCM:with the help of a stereoscope,the distribution of the PCM in the samples was analyzed.Adhesion test:the adhesion between the metal sheets and the polyurethane foam was measured following the UNE 41950procedure,in order to validate if the values were within the limits.Thermal performance test:the measurements were performed in two experimental installations,at the University of Zaragoza [14](Fig.4)and at the University of Barcelona.In these experiments,the evolution of the temperature with time was measured,against an air flow (Fig.4)[15].Fig.1.View of the sandwichpanel.Fig.2.Manufacture of the sandwich panel with PCM (case2).Fig.3.Manufacture of the sandwich panel with PCM (case 3).C.Castellón et al./Renewable Energy 35(2010)2370e 237423713.Results3.1.Results for case 1Fig.5shows the distribution of the PCM through the foam (case 1).A homogeneous distribution of the PCM microcapsules can be observed;this uniformity was expected because the PCM was included in the polyurethane formulation.Fig.6shows thermal performance results for case 1(reference sample and sample with PCM).The figure shows the air flow temperature (around 34.5 C)at which the samples were tested.The temperature behaviour of the insulated surface shows a faster heating of the sample with PCM.For example,to reach 32 C,the sample with PCM needs about 400s more than the reference sample.This result is in contradiction with the expected effect of increased thermal inertia and can be explained by an increase of the effective thermal conductivity of the insulation due to the presence of solid particles.The adhesion test results can be seen in Table 2.In this case,the reference sample and the sample with PCM are within the limits for strength established by the standard UNE 41950(L.MAX >0.10MPa).3.2.Results for case 2Fig.7(a)shows the PCM distribution through the foam for case 2.In general,the distribution of the PCM was not homogeneous;the microcapsules are concentrated close to the metal sheet (free surface)and in some areas in the middle of the foam (foam with a whitish colour).Small cracks in the polyurethane can be observed,and microcapsules of PCM were observed within these cracks (Fig.7(b)).Fig.7(c)shows an image of the reference sample.Small cracks that do not contain PCM can be observed (Fig.7(d)).Fig.8shows the results of the thermal performance test for case paring the insulated surfaces,the sample with PCM does not show the expected effect (higher thermal inertia).A faster heating,with a time delay to reach 32 C in about 100s,between the sample with PCM and the reference sample can be seen.The same proce-dure was followed with two different samples and the results were one similar to the previous sample,and the second one with the expected effect (it shows a delay in the temperature evolutionofFig.5.Case 1:(a)sandwich panel with PCM;and (b)zoom of the sample withPCM.Fig.4.Experimental installation to measure the temperature evolution in a solid sample (University of Zaragoza).X 1¼free surface (external surface);X 2¼insulated surface (internal surface).Table 1Properties of Micronal BASF as given by the manufacturer.Micronal BASF PCM Melting temperature w 26 C Phase change enthalpy 100kJ/kg Microcapsules size5mmFig.6.Thermal performance test of the reference sandwich panel and sandwich panel with PCM (case 1).C.Castellón et al./Renewable Energy 35(2010)2370e 23742372the PCM sample).These results may be attributed to the poor distribution of the PCM or even to the possibility that the sample tested does not contain PCM,because of the inhomogeneous distribution previously observed.Even though,the results obtained in the third sample reveal that the possibility of increasing thermal inertia due to the inclusion of PCM was demonstrated.3.3.Results for case 3Case 3shows a different distribution of the PCM microcapsules that are concentrated close to the metal sheet,and also small areas with PCM at the middle of the foam (whitish cracks)were found;see Fig.9(a)and (b).As seen in these figures,it seems that in this case there were fewer cracks than previously.Fig.10shows the results of the thermal performance test for case 3.The sample with PCM achieved the same temperature of the reference sample (32 C)about 450s later.Due to an increase of thermal inertia,this effect is expected when the PCM is used.Table 2shows the adhesion results of case 1,case 2and case 3.In all cases,the reference samples are within or close to the limits (0.1MPa is the minimum load for adhesion test in sandwich panels).Adhesion results of the sandwich panel with PCM are out of the limits.During the performance of the adhesion test,the failure of the reference sample is always between the metal sheet and the foam,but for the sample with PCM (case 2)the failurewas in the middle of the foam and at a much lower stress,revealing that PCM microcapsules are acting as stress concen-trators within the foam.For the results with PCM (case 3)these are far below the limit.4.DiscussionThe objective of this work was to demonstrate the feasibility of using microencapsulated PCM in sandwich panels to increase their thermal inertia.The main problem lies on how to include the micro-encapsulated PCM ful filling standards of the conventional sand-wich panel.Therefore,different manufacturing cases to implement the PCM were tested.For every case three different analyses were realized:the distribution of the PCM through the foam,an adhesion test,and a thermal performance test comparing samples with and without PCM.In case 1,the distribution of the microcapsules is homogeneous throughout the foam,but it seems as the effect of the PCM is overlapped by a possible increase in thermal conductivity of the polyurethane (due to the increase of solids in the formulation).A faster heating of the sample with PCM can be observed.Results of adhesion test were not a problem because they are within the limits,the distribution of the microcapsules helped to get an acceptable result.In case 2,the distribution of the PCM was concentrated close to the metal sheet (external surface)and in some areas in the middle of the foam.For thermal performance test,three samples were analyzed.Two of them presented an unexpected faster heating of the sample with PCM and a third sample showed the expected increase of thermal inertia in the sample with PCM,giving a time delay of 450s to reach 32 C.Such a variety of results may be explained due to the poor distribution of the PCM in the foam.Results of adhesion test are out of the limits because the failure of sample with PCM occurs within the foam.In case 3,the distribution of the PCM was concentrated close to the metal sheet (internal surface)and in some areas of the foam.A higher thermal inertia in the sample with PCM can be observed.Problems were found in the adhesion test,similar to case 2.A possible solution of this process could be a located dosage of the PCM during the process that could concentrate the microcapsules close to the metal sheet even aided by anadhesive.Fig.7.Case 2:(a)sandwich panel with PCM;(b)zoom of the sample with PCM;(c)reference sample;and (d)zoom of the referencesample.Table 2Fig.8.Thermal performance test of the reference sandwich panel and sandwich panel with PCM (case 2).C.Castellón et al./Renewable Energy 35(2010)2370e 237423735.Concluding remarksThe goal of this study was to demonstrate the feasibility of using a microencapsulated PCM (Micronal BASF)in sandwich panels to increase its thermal inertia,and to reduce the energy demand of the final buildings.The results shown above include different manufacturing processes and the results obtained with case 1was the expected,the PCM effect is overlapped by a possible increase in thermal conductivity,case 2and case 3show the feasibility of using a microencapsulated PCM in panel sandwich increasing its thermal inertia and without substantial increase of the weight of the sandwich panel with the inclusion of PCM.In both cases (2and 3),the industrialisation of the process to improve the results is required.The possibility of adapting this technology to manufac-ture panels allows their installation on ceilings and walls.AcknowledgmentsThe work was partially funded by the Spanish government (project ENE2008-06687-C02-01/CON)and the European Union (COST Action COST TU0802),in collaboration with the companiesEuroper fil and PLASFI.The authors 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