临床肝移植时,若供肝为脂肪肝常并发移植后肝原发无功能,导致患者死亡或再次肝移植,如何降低其移植后原发无功能发生是目前亟待解决的关键问题。本项目在原有工作基础上,拟构建靶向调控脂肪肝中解偶联蛋白-2(UCP-2)表达并与逆转录病毒体重组的质粒,在正常与肥胖小鼠(肝脂肪含量约70%-80%)体外培养肝细胞、缺血/再灌注及移植模型中转染。采用荧光素酶法、速率法、RT-PCR、Western blot、流
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数据更新时间:2023-05-31
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