欢迎来到天天文库
浏览记录
ID:34180470
大小:51.00 KB
页数:6页
时间:2019-03-04
《肝星状细胞论文熊果酸对大鼠肝星状细胞nox亚基p(phox)及其调控的下游信号通路的影响》由会员上传分享,免费在线阅读,更多相关内容在教育资源-天天文库。
1、肝星状细胞论文:熊果酸对大鼠肝星状细胞NOX亚基p47(Phox)及其调控的下游信号通路的影响【中文摘要】肝纤维化是肝脏慢性损伤后的一种普遍现象,最终导致细胞外基质(extracellularmatrix,ECM)在肝脏中过度沉积。瘦素是一个重要的促肝纤维化因子,它与HSC上的Ob受体结合后,引起Janus激酶(Januskinase,JAK)磷酸化及JAK-信号转导及转录激活因子(signaltransducersandactivatorsoftranscriptionfactor,STAT)的活化。JAK还通过激活【英文摘要】Background:Hepaticfibrosisi
2、sauniversalphenomenonofchronicityliverinjurywhicheventuallyleadtotheextracellularmatrixdepositionintheliver.Leptinisanimportantfactorthatcanpromotetheliverfibrosisandcausephosphorylationofjanuskinase(JAK)andJAK-signaltransducersandactivationoftranscriptionfactor(STAT)bybindingwithobacceptorinHS
3、Cs.JAKactivatesreducedformofnicotinamide-adeninedinucleotidephosphateoxidase(NADPHoxidase,NOX)andthereduction-oxidation-sensitivecellssignalingpathwaysProteinkinaseB(AKT)andextracellularsignal-regulatedkinase(ERK)bygeneratingreactiveoxygenspecies(ROS).leadingtothesignalingcascadeandgeneexpressi
4、onrelatedtothefibrosisandinflammation.Previously,6/6weperformedthestudythatUrsolicAcid(UA)couldsignificantlyimprovelivertissuestructureofhepaticfibrosisinvivo,andbetterthancolchicine.ItcouldinhibittheproliferationofHSCsandinducetheapoptosisofHSCsinvitro.PretreatmentwithUAcouldinhibitNOXsubunitp
5、22PhoxandRaclmRNAandROSinducedbyleptinandactivationofnuclearfactor-KB,andsubsequentlyinducetheapoptosisofHSCs.Inthisstudy,wellobserveeffectsofUAonNOXsubunitp47phoanditsdownstreamsignalingpathwayERK1/2inducedbyleptininHSCs,andexpressionofcollagen1.:ToexploretheeffectsofUAonNOXsubunitp47phoxandit
6、sdownstreamsignalingpathwayERK1/2inducedbyleptininHSCs(HSC-T6),andproliferationofHSCsandexpressionofECM.Methods:HSC-T6intheexponentialgrowthphaseweredevided:normalcontrolgroup;leptin(100ng/ml)treated;leptintreatedtogetherwithUA(50μM);leptintreatedtogetherwithJAKinhibitorAG490(50μM);leptintreate
7、dtogetherwithNOXinhibitorDPI(20μM)andleptintreatedtogetherwithERKinhibitorPD98059(30μM).HSC-T6weretreatedwithmedicinefor30minutesandmembraneproteinandphosphorylationproteinexpressionofp47phoxandERK1/2wereanalyzedwithwesternblottin
此文档下载收益归作者所有