Yamamoto N, Maki A, Swann J D, Berezesky I K, Trump B F
Department of Pathology, University of Maryland, School of Medicine, Baltimore.
Ren Fail. 1993;15(2):163-71. doi: 10.3109/08860229309046148.
This study was designed to investigate the influence of intracellular ionized calcium ([Ca2+]i) on the induction of c-fos, c-jun, c-myc, and hsp70 genes after oxidant stress induced by xanthine/xanthine oxidase (X/XOD) treatment or after heat shock using primary cultures of rat proximal tubule epithelium (PTE). X/XOD (500 microM/25 mU/mL) induced all of these genes; ionomycin also resulted in similar kinetics of induction of all genes. The expression of both c-fos following X/XOD treatment and hsp70 following heat shock was markedly decreased through chelation of [Ca2+]i by Quin 2/AM. The c-fos expression following X/XOD treatment was partly reduced by a protein kinase C inhibitor, staurosporine (ST), and markedly inhibited by another protein kinase inhibitor, 2-aminopurine (2AP), while both ST and 2AP markedly reduced hsp70 expression. The ADP-ribosylation transferase inhibitor 3-aminobenzamide had no effect on either c-fos or hsp70 expression. These results suggest that cell injuries leading to increased [Ca2+]i in PTE result in induction of c-fos, c-jun, c-myc, and hsp70; and that the activation of c-fos and hsp70 genes may be regulated by [Ca2+]i and [Ca2+]i-dependent protein kinases.
本研究旨在探讨细胞内游离钙([Ca2+]i)对黄嘌呤/黄嘌呤氧化酶(X/XOD)处理诱导的氧化应激后或热休克后大鼠近端肾小管上皮细胞(PTE)原代培养物中c-fos、c-jun、c-myc和hsp70基因诱导的影响。X/XOD(500 microM/25 mU/mL)诱导了所有这些基因;离子霉素也导致所有基因的诱导动力学相似。通过用喹啉2/AM螯合[Ca2+]i,X/XOD处理后的c-fos表达和热休克后的hsp70表达均明显降低。X/XOD处理后的c-fos表达被蛋白激酶C抑制剂星形孢菌素(ST)部分降低,并被另一种蛋白激酶抑制剂2-氨基嘌呤(2AP)显著抑制,而ST和2AP均显著降低hsp70表达。ADP-核糖基转移酶抑制剂3-氨基苯甲酰胺对c-fos或hsp70表达均无影响。这些结果表明,导致PTE中[Ca2+]i升高的细胞损伤会导致c-fos、c-jun、c-myc和hsp70的诱导;并且c-fos和hsp70基因的激活可能受[Ca2+]i和[Ca2+]i依赖性蛋白激酶的调节。