RP-8和TRPM-2基因的表达在半乳糖胺损伤后增加

Mark J. Czaja , Yang Xu , Teija Oinonen , Kai O. Lindros
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摘要

研究了大鼠肝毒素半乳糖胺(GalN)损伤后肝细胞凋亡在肝细胞死亡中的作用。组织学证据表明,给药后肝细胞弥漫性凋亡。由于细胞凋亡是一种活跃的细胞死亡形式,通常需要新的基因表达,因此确定与细胞凋亡相关的基因是否在GalN肝损伤后表达。正常肝脏中与其他器官细胞凋亡相关的两个基因RP-8和TRPM-2表达,在GalN损伤后其mRNA水平升高。这些基因在肝细胞中表达,没有任何小叶内的表达梯度。与GalN肝损伤相比,RP-8和TRPM-2水平在大鼠部分肝切除术后的纯粹增殖反应期间不变。这些数据表明肝细胞组成性地表达包括RP-8和TRPM-2基因在内的凋亡遗传程序。中毒性肝损伤进一步刺激这些基因表达的能力可能导致肝细胞凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RP-8 and TRPM-2 gene expression is constitutive in rat liver and increased following galactosamine injury

The contribution of apoptosis to hepatocyte cell death after rat liver injury from the hepatotoxin galactosamine (GalN) was examined. Histologic evidence of diffuse hepatocyte apoptosis existed after GalN administration. Since apoptosis is an active form of cell death usually requiring new gene expression, it was determined whether genes associated with apoptosis were expressed following GalN liver injury. RP-8 and TRPM-2, two genes associated with apoptosis in other organs, were expressed in normal liver, and their mRNA levels increased after GalN injury. These genes were expressed in hepatocytes without any intralobular zonal gradient in expression. In contrast to GalN liver injury, RP-8 and TRPM-2 levels were unchanged during the purely proliferative response following rat partial hepatectomy. These data suggest that hepatocytes constitutively express the genetic program for apoptosis including the RP-8 and TRPM-2 genes. The ability of toxic liver injury to further stimulate expression of these genes may lead to apoptotic hepatocyte cell death.

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