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Hepatic mitochondrial transport of glutathione: Studies in isolated rat liver mitochondria and H4IIE rat hepatoma cells

机译:谷胱甘肽的肝线粒体转运:大鼠肝线粒体和H4IIE大鼠肝癌细胞的分离研究

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摘要

Glutathione (GSH) is transported into renal mitochondria by the dicarboxylate (DIC; Slc25a10) and 2-oxo-glutarate carriers (OGC; Slc25a11). To determine whether these carriers function similarly in liver mitochondria, we assessed the effect of competition with specific substrates or inhibitors on GSH uptake in isolated rat liver mitochondria. GSH uptake was uniphasic, independent of ATP hydrolysis, and exhibited Km and Vmax values of 4.08 mM and 3.06 nmol/min per mg protein, respectively. Incubation with butylmalonate and phenylsuccinate inhibited GSH uptake by 45–50%, although the individual inhibitors had no effect, suggesting in rat liver mitochondria, the DIC and OGC are only partially responsible for GSH uptake. H4IIE cells, a rat hepatoma cell line, were stably transfected with the cDNA for the OGC, and exhibited increased uptake of GSH and 2-oxoglutarate and were protected from cytotoxicity induced by H2O2, methyl vinyl ketone, or cisplatin, demonstrating the protective function of increased mitochondrial GSH transport in the liver.
机译:谷胱甘肽(GSH)通过二羧酸盐(DIC; Slc25a10)和2-氧代戊二酸载体(OGC; Slc25a11)转运至肾线粒体。为了确定这些载体在肝线粒体中是否具有相似的功能,我们评估了与特定底物或抑制剂竞争对离体大鼠肝线粒体中GSH吸收的影响。 GSH吸收是单相的,与ATP水解无关,并且每mg蛋白质的Km和Vmax值分别为4.08 mM和3.06 nmol / min。与丙二酸丁酯和丁二酸苯酯一起孵育可抑制GSH摄取45–50%,尽管单个抑制剂没有作用,这表明在大鼠肝线粒体中,DIC和OGC仅部分负责GSH摄取。大鼠肝癌细胞系H4IIE细胞已被OGC的cDNA稳定转染,并显示出GSH和2-氧代戊二酸的摄取增加,并受到H2O2,甲基乙烯基酮或顺铂诱导的细胞毒性的保护,证明了H4IIE细胞的保护功能。肝脏中线粒体GSH转运增加。

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