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  • 简介:Thispaperaimstotheresearchoftheimpactoffluidshearstressontheadhesionbetweenvascularendothelialcellsandleukocyteinducedbytumornecrosisfactor-α(TNF-α)bymicrofliudicchiptechnology.Microfluidicchipwasfabricatedbysoftlithograph;Endothelialmicrofluidicchipwasconstructedbyoptimizingtypesoftheextracellularmatrixproteinsmodifiedinthemicrochannelandcellincubationtime;humanumbilicalveinendothelialcellsEA.Hy926linedinthemicrochannelwereexposedtofluidshearstressof1.68dynes/cm~2and8.4dynes/cm~2respectively.Meanwhile,adhesionbetweenEA.Hy926cellsandleukocytewasinducedbyTNF-αunderaflowcondition.EA.Hy926cellculturedinthestaticconditionwasusedascontrolgroup.Thenumbersoffluorescently-labeledleukocyteinmicrochannelwerecountedtoquantizetheadhesionlevelbetweenEA.Hy926cellsandleukocyte;cellimmunofluorescencetechniquewasusedtodetecttheintercellularadhesionmolecule(ICAM-1)expression.TheconstructedendothelialmicrofluidicchipcanaffordtothefluidshearstressandrespondtoexogenousstimulusofTNF-α;comparedwiththeadhesionnumbersofleukocyteincontrolgroup,adhesionbetweenEA.Hy926cellsexposedtolowfluidshearstressandleukocytewasreducedunderthestimulusofTNF-αataconcentrationof10ng/ml(P<0.05);leukocyteadhesionwithEA.Hy926cellsexposedtohighfluidshearstresswasreducedsignificantlythanEA.Hy926cellsincontrolgroupandEA.1Hy926cellsexposedtolowfluidshearstress(P<0.01);theregulationmechanismoffluidshearstresstotheadhesionbetweenEA.Hy926cellsandleukocyteinducedbyTNF-αwasthroughthewayofICAM-1.Theendothelialmicrofluidicchipfabricatedinthispapercouldbeusedtostudythefunctionsofendothelialcellinvitroandprovideanewtechnicalplatformforexploringthepathophysiologyoftherelatedcardiovascularsystemdiseasesunderaflowenvironment.

  • 标签: 微血管内皮细胞 肿瘤坏死因子-α 微流控芯片 剪切应力 白细胞 芯片技术
  • 简介:目的探讨NF—κB抑制剂PDTC对高分予量聚乙烯磨损颗粒(UHMWPE)诱导的假体周围界膜组织产生TNF—α的影响,寻找防治假体周围骨溶解的方法。方法用昆明小鼠24只构建air—pouch模型,随机分成两组,每组8只,阳性对照组(囊内注入UHMWPE颗粒悬液,腹腔注射生理盐水);实验组(囊内注入UHMWPE颗粒悬液,腹腔注射PDTC),阴性对照组(囊内注入生理盐水,腹腔注射PDTC),7天后处死动物,ELISA法检测囊壁组织中TNF—α的含量。结果阳性对照组囊壁组织TNF—α含量为6.3429±0.7475(OD/克);实验组囊壁组织中TNF—α含量为5.0428±0.8105;阴性对照组囊壁中TNF-α含量为3.5010±0.7248。其中阳性对照组与实验组、阳性对照组与阴性对照组、实验组与阴性对照组之间两两对比均有显著统计学差异(P〈0.01)。结论NF—κB抑制剂PDTC能够抑制UHMWPE颗粒诱导的界膜组织中TNF—α的产生,对假体周围骨溶解有防治作用。

  • 标签: 磨损颗粒 无菌性松动 PDTC TNF—α