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作 者:林恒[1] 唐春[1] 吴乔[1] 冯春林[1] 张玉君[1] 别平[1]
机构地区:[1]第三军医大学西南医院全军肝胆外科研究所,重庆400038
出 处:《第三军医大学学报》2009年第22期2220-2224,共5页Journal of Third Military Medical University
基 金:国家自然科学基金(30571806;30872494)~~
摘 要:目的初步探讨线粒体转录因子A(mitochondrial transcription factor A,TFAM)在重组人肝再生增强因子(rhALR)对梗阻性黄疸大鼠肝功能保护过程中的作用。方法首先体外合成靶向TFAM的有效慢病毒载体,然后建立梗阻性黄疸大鼠动物模型,并通过门静脉将慢病毒注入大鼠肝组织进行靶向TFAM活体RNA干扰实验。然后通过RT-PCR和Western blot检测目的基因表达量的改变并观察大鼠肝脏病理改变、肝脏功能改变及rhALR保护作用的变化情况。结果体外靶向TFAM慢病毒载体构建成功。通过门静脉注入后能特异、有效的感染肝组织细胞。RT-PCR和Western blot检测结果显示进行活体RNAi的大鼠肝组织中TFAM的表达明显减弱;且这一组大鼠肝脏病理改变最为明显,肝功能损害最严重,rhALR的肝功能保护作用也随着消失。结论阻断目的基因TFAM的表达使得rhALR对梗阻性黄疸大鼠肝功能的保护作用消失;TFAM在rhALR保护梗阻性黄疸大鼠肝功能过程中具有重要作用。Objective To explore the role of mitochondrial transcription factor A(TFAM) in protecting the hepatic function of rats with obstructive jaundice by recombinant human augmenter of liver regeneration(rhALR).Methods The effective lentivirus-siRNA vector system targeting TFAM was successfully constructed in vitro.Then we established obstructive jaundice rat model and the lentivirus-siRNA vector was infused into the liver through portal vein for RNAi in vivo.RT-PCR and Western blot analysis were used to detect the change of TFAM expression. Liver pathology, hepatic function and the effect of rhALR were studied. Results Liver cells were specially and effectively transfected by lentivirus-siRNA vector. The results of RT-PCR and Western blotting showed that TFAM expression was obviously suppressed. The knockdown of target gene led to obviously changed hepatic pathology and severely damaged hepatic function. The protective effect of rhALR also disappeared. Conclusion The protective effect of rbALR on hepatic function disappeared after the suppression of TFAM. TFAM gene is very important for rhALR to exert its protective effect on hepatic function in rats with obstructive jaundice.
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