癌变·畸变·突变
癌變·畸變·突變
암변·기변·돌변
CARCINOGENSES,TERATOGENSIS AND MUTAGENESIS
2014年
5期
339-342,347
,共5页
孙平楠%周小玲%杨少哲%程琳%姚伟城
孫平楠%週小玲%楊少哲%程琳%姚偉城
손평남%주소령%양소철%정림%요위성
人胚胎干细胞%肝细胞%HBV研究模型
人胚胎榦細胞%肝細胞%HBV研究模型
인배태간세포%간세포%HBV연구모형
human embryonic stem cell%hepatocytes%HBV model
目的:初步探索应用人胚胎干细胞来源的肝细胞作为乙肝病毒(HBV)体外研究模型的潜力。方法:定向分化人胚胎干细胞为肝细胞(hESC-Heps);采用免疫荧光方法检测肝性因子如肝细胞核因子-4α(HNF4α)、白蛋白(ALB)和HBV功能性受体钠离子/牛磺胆酸共转运蛋白(NTCP)受体的表达;实时荧光定量PCR检测Ⅲ型干扰素受体表达,Western blotting 检测hESC-Heps在Ⅲ型干扰素刺激下干扰素通路中磷酸化转录信号传导子与激活子2(STAT2)的表达。结果:成熟的hESC-Heps表达肝性因子HNF4α和ALB,表达HBV功能性受体NTCP受体,并且具有人原代肝细胞特异性的Ⅲ型干扰素反应。结论:人胚胎干细胞来源的肝细胞hESC-Heps可能成为一种具有潜力的HBV研究模型。
目的:初步探索應用人胚胎榦細胞來源的肝細胞作為乙肝病毒(HBV)體外研究模型的潛力。方法:定嚮分化人胚胎榦細胞為肝細胞(hESC-Heps);採用免疫熒光方法檢測肝性因子如肝細胞覈因子-4α(HNF4α)、白蛋白(ALB)和HBV功能性受體鈉離子/牛磺膽痠共轉運蛋白(NTCP)受體的錶達;實時熒光定量PCR檢測Ⅲ型榦擾素受體錶達,Western blotting 檢測hESC-Heps在Ⅲ型榦擾素刺激下榦擾素通路中燐痠化轉錄信號傳導子與激活子2(STAT2)的錶達。結果:成熟的hESC-Heps錶達肝性因子HNF4α和ALB,錶達HBV功能性受體NTCP受體,併且具有人原代肝細胞特異性的Ⅲ型榦擾素反應。結論:人胚胎榦細胞來源的肝細胞hESC-Heps可能成為一種具有潛力的HBV研究模型。
목적:초보탐색응용인배태간세포래원적간세포작위을간병독(HBV)체외연구모형적잠력。방법:정향분화인배태간세포위간세포(hESC-Heps);채용면역형광방법검측간성인자여간세포핵인자-4α(HNF4α)、백단백(ALB)화HBV공능성수체납리자/우광담산공전운단백(NTCP)수체적표체;실시형광정량PCR검측Ⅲ형간우소수체표체,Western blotting 검측hESC-Heps재Ⅲ형간우소자격하간우소통로중린산화전록신호전도자여격활자2(STAT2)적표체。결과:성숙적hESC-Heps표체간성인자HNF4α화ALB,표체HBV공능성수체NTCP수체,병차구유인원대간세포특이성적Ⅲ형간우소반응。결론:인배태간세포래원적간세포hESC-Heps가능성위일충구유잠력적HBV연구모형。
OBJECTIVE: To explore the potential of human embryonic stem cell-derived hepatocytes (hESC-Heps) for hepatitis Bvirus ( HBV) model.METHODS:Human embryonics temcells were directly induced to differentiate into hESC-Heps using a step-wised method. Expression of hepatocyte-enriched factors such as hepatocyte nuclear factor 4 alpha+(HNF4α) and albumin (ALB),and HBV functional receptor Na/taurocholate cotransporting polypeptide (NTCP) receptor in hESC-Heps were examined by immunofluorescence method. Moreover,activation of signal transducer and activator of transcription 2 (STAT2) in hESC-Heps treated with typeⅢ interferon was examined by Western blotting.RESULTS:Mature hESC-Heps expressed HNF4α,ALB,and NTCP receptor as well as displayed typeⅢ interferon responsespecific in primary human hepatocytes.CONCLUSION:hESC-Heps maybe a potential model for HBV research.