Hatayama I, Yamada Y, Tanaka K, Ichihara A, Sato K
Second Department of Biochemistry, Hirosaki University School of Medicine.
Jpn J Cancer Res. 1991 Jul;82(7):807-14. doi: 10.1111/j.1349-7006.1991.tb02706.x.
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 1-chloro-2,4-dinitrobenzene and 1,2-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 blot analysis of GSTs revealed that GST-P, which is not present in freshly isolated hepatocytes, was markedly induced and that GST subunits 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 be regulated by JUN and FOS proteins.
在无血清培养基中原代培养的大鼠肝细胞中,研究了表皮生长因子(EGF,10 ng/ml)和胰岛素(100 nM)对谷胱甘肽S-转移酶(GSTs)表达的影响,特别是GST-P形式(GST 7-7)。用EGF和胰岛素培养时,对1-氯-2,4-二硝基苯和1,2-二氯-4-硝基苯的GST活性在第2天短暂下降至新鲜分离肝细胞活性的10%,然后在第4天增加至新鲜分离细胞活性的60%至100%。对GSTs的蛋白质印迹分析显示,新鲜分离的肝细胞中不存在的GST-P被显著诱导,并且添加EGF和/或胰岛素后,Mu类的GST亚基3和4也增加,而Alpha类的亚基1和2消失。RNA印迹分析表明,添加EGF和胰岛素后,GST-P mRNA水平也升高,并且核原癌基因c-jun和c-fos的表达增强。这些结果表明,EGF或胰岛素在原代培养的大鼠肝细胞中诱导的GST-P表达增强可能受JUN和FOS蛋白调控。