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Induction of Glutathione S‐Transferase P‐Form in Primary Cultured Rat Hepatocytes by Epidermal Growth Factor and Insulin

机译:表皮生长因子和胰岛素诱导原代培养的大鼠肝细胞中谷胱甘肽S-转移酶P-形式的诱导

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摘要

The effects of epidermal growth factor (EGF) (10 ng/ml) and insulin (100 nM) on the expression of glutathione S‐transferases (GSTs), especially the GST‐P form (GST 7–7), were examined in primary cultured rat hepatocytes in serum‐free medium. On culture with EGF and insulin, the GST activities towards l‐chloro‐2,4‐dinitrohenzene and l,2‐dichloro‐4‐nitrobenzene were transiently decreased on day 2 to 10% of those of freshly isolated hepatocytes and then increased to 60 to 100% of those of freshly isolated cells on day 4. Western hlot analysis of GSTs revealed that GST‐P, which is not present in freshly isolated hepatocytes, was markedly induced and that GST subimits 3 and 4 of the Mu class also increased after addition of EGF and/or insulin, while the subunits 1 and 2 of the Alpha class disappeared. Northern blot analysis showed that on addition of EGF and insulin the level of GST‐P mRNA was also elevated and expressions of the nuclear oncogenes c‐jun and c‐fos were enhanced. These results suggest that the enhanced expression of GST‐P induced by EGF or insulin in primary cultured rat hepatocytes might he regulated by JUN and FOS proteins.
机译:在初次检查中,检查了表皮生长因子(EGF)(10 ng / ml)和胰岛素(100 nM)对谷胱甘肽S-转移酶(GST),特别是GST-P形式(GST 7-7)表达的影响。无血清培养基中培养的大鼠肝细胞。在用EGF和胰岛素进行培养时,对L-氯-2,4-二硝基苯和L,2-二氯-4-硝基苯的GST活性在第2天瞬时下降,降至新鲜分离的肝细胞的GST活性的10%,然后增加到60在第4天达到新鲜分离细胞的100%。蛋白质GST的蛋白质印迹分析表明,新鲜分离的肝细胞中不存在的GST-P被显着诱导,Mu类的GST亚基3和4在之后也有所增加加入EGF和/或胰岛素,而Alpha类的亚基1和2消失了。 Northern印迹分析表明,添加EGF和胰岛素后,GST-P mRNA的水平也升高,并且核致癌基因c-jun和c-fos的表达增强。这些结果表明,EGF或胰岛素诱导的原代培养大鼠肝细胞中GST-P的表达增强可能受JUN和FOS蛋白的调节。

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