rhorock信号通路介导缺氧所致人肺微血管内皮细胞肌动蛋白细胞骨架重构和重组人白介素10对缺氧条件下人肺微血管内皮细胞凋亡变化规律的影响.docx
-
资源ID:1472770
资源大小:9.66KB
全文页数:2页
- 资源格式: DOCX
下载积分:5金币
友情提示
2、PDF文件下载后,可能会被浏览器默认打开,此种情况可以点击浏览器菜单,保存网页到桌面,就可以正常下载了。
3、本站不支持迅雷下载,请使用电脑自带的IE浏览器,或者360浏览器、谷歌浏览器下载即可。
4、本站资源下载后的文档和图纸-无水印,预览文档经过压缩,下载后原文更清晰。
5、试题试卷类文档,如果标题没有明确说明有答案则都视为没有答案,请知晓。
|
rhorock信号通路介导缺氧所致人肺微血管内皮细胞肌动蛋白细胞骨架重构和重组人白介素10对缺氧条件下人肺微血管内皮细胞凋亡变化规律的影响.docx
rhorock信号通路介导缺氧所致人肺微血管内皮细胞肌动蛋白细胞骨架重构和重组人白介素10对缺氧条件下人肺微血管内皮细胞凋亡改变规律的影响广州医学院硕士学位论文5Hypoxia-InducedReorganizationofActinCytoskeletonMediatedbyRho-ROCKSignalPathwayinHumanPulmonaryMicrovascularEndothelialCellsandTheEffectofRecombinationHumanInterleukin10onHypoxia-inducedApoptosisinHumanPu1nonaryMicrovascularEndothelialCellsProf.Qi-IiangCuiCandidate:JingMoSupervisor:Abstract1Objective1.1ToinvestigatetheroleofRho-ROCKsignalpathwayinthereorganizationofactincytoskeletonandthechangesofmorphologyinducedbyhypoxiainhumanpulmonarymicrovascularendothelialcelIs(HPMVECs).1.2Toinvestigatetheameliorativemechanismofrecombinatinghumaninterleukin10(rhI1.-10)throughinhibitingtheapoptosisandCaSPaSe-3activityinhypoxia-inducedhumanpulmonarymicrovascularendothelialcelIs.2MaterialsandMethods2.1Duringtheexperimentsthehumanpulmonarymicrovascularendothelialcellswereexposedtohypoxiafor6h,12hand24hrespectivelyorpre-incubatedwithaspecialinhibitorofKOCK,H-1152(10nmol1.)for0.5hbeforehypoxiainvitro.ThereorganizationofcellularactincytoskeletonandthechangesofcellularmorphologyinducedbyhypoxiaorpretreatmentofHl152wereexaminedbylaserscanningconfocal广州医学院硕士学位论文6microscopy(1.SCM).TheF-actinmeanfluorescenceintensityofeachgroupwasexaminedbyflowcytometric.2.2TheculturedHPMVECswererandomizedtonormalcontrolgroup,hypoxiacontrolgroup,thelow-rhI1.-10interventiongroup,middle-rhI1.-10interventiongroupandhigh-doserhI1.-10interventiongroup.Thenormalgroupwasculturedwiththe37eCand5%CO2condition,andthehypoxiagroupswereculturedwith5%CO2,95%N2condition.Theculturedtimelastedfor4h,12h,24hand48hrespectively.Therelativecaspase-3activityofal1groupsweredetectedwithChromatometryattheendof4h,12h,24hand48h.Theapoptosisfluorescenceintensitywereanalyzedbythefluorescentmicroscopeattheendof24hwithstatisticalmet.