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作 者:张莉娟[1] 何彬彬[1] 黄月红[1] 陈治新[1] 王小众[1]
机构地区:[1]福建医科大学附属协和医院消化内科,福州350001
出 处:《中华实验外科杂志》2015年第12期3032-3034,共3页Chinese Journal of Experimental Surgery
基 金:福建省临床医学重点专科资助项目(闽卫科教[2012]149号)
摘 要:目的观察肝素结合性表皮生长因子样生长因子(HB-EGF)激活大鼠肝星状细胞(HSC—T6)过程中微小RNA(miRNA,miR)-221、miR-222表达的变化,探讨miR-221/222在肝星形细胞(HSC)活化过程中的作用。方法培养、接种HSC—T6,分别以HB—EGF和细胞外信号调节激酶(ERK)特异性抑制剂PD98059+HB—EGF共处理HSC—T624、48h,采用实时定量反转录聚合酶链反应(RT—qPCR)法检测miR-221/222表达水平。结果对照组、HB—EGF组及共处理组(48h)miR-221表达水平分别为0.90±0.14、1.08±0.09和0.71±0.14,miR-222表达水平分别为0.82±0.10、1.04±0.09和0.68±0.16。说明HB—EGF可促进miR-221、miR-222的表达,ERK抑制剂可使miR-221、miR-222表达下降(P〈0.01)。结论HB—EGF通过激活HSC—T6的Ras/ERK信号通路,继而促进miR-221、miR-222的表达,参与HSC活化的调控。Objective To study the effect of heparin - binding epidermal growth factor (HB -EGF) on the expression of microRNA (miRNA, miR) -221/222 for exploring the regulatory roles of miR -221/222 in the activation of hepatic stellate cells (HSC). Methods The rat HSC -T6 cells were treated with HB - EGF and PD98059 HB - EGF for 24 or 48 h. The expression of miR - 221 and miR -222 mRNA was detected by real- time quantitative reverse transcriptase -polymerase chain reaction ( RT - qPCR). Results RT - qPCR showed the level of miR - 221 in control group, HB - EGF group and co -cultured group was 0. 90 ±0. 14, 1.08 ±0. 09 and 0. 71±±0. 14 respectively, and that of miR -222 was O. 82 ±0. 10, 1.04 ± 0. 09 and 0. 68 ± 0. 16 respectively. The expression levels of miR - 221 and miR - 222 were significantly increased in HSC - T6 cells treated with HB - EGF, and those were decreased in HSC - T6 cells co - cultured with PD98059 and HB - EGF, as compared with control group ( P 〈 0. 01 ). Conclusion HB - EGF participates in the regulation of HSC activation by activating Ras/Extracel- lular sigual regulated kinase (ERK) signal transduction pathway in HSC -T6 cells and subsquently accel- erating the expression of miR- 221/222.
关 键 词:肝星状细胞 肝素结合性表皮生长因子样生长因子 Ras/细胞外信号调节激酶信号通路 微小RNA-221 微小RNA-222
分 类 号:R758.63[医药卫生—皮肤病学与性病学]
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