Kharbanda S, Nakamura T, Kufe D
Laboratory of Clinical Pharmacology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.
Biochem Pharmacol. 1993 Feb 9;45(3):675-81. doi: 10.1016/0006-2952(93)90142-j.
The present work demonstrates that ethanol induces expression of the c-jun proto-oncogene in human keratinocytes. Increased c-jun mRNA levels were detectable at 1 hr of exposure to 1% ethanol and at 24 hr remained above that in control keratinocytes. An increase in c-jun expression was also detectable at ethanol concentrations of 0.1 and 0.5%. Similar findings were obtained for the related jun-B and c-fos early response genes. The results also demonstrate that ethanol exposure is associated with increases in protein kinase C activity in both the cytosol and membrane fractions. This increase was detectable at 5 min and maximal at 30-60 min. The finding that induction of c-jun expression by ethanol was inhibited by the isoquinolinesulfonamide derivative H7, but not by HA1004, suggested that this effect is mediated by protein kinase C. Furthermore, down-regulation of protein kinase C by prolonged exposure to 12-O-tetradecanoylphorbol-13-acetate was associated with a block in ethanol-induced c-jun expression. We also demonstrated that ethanol exposure is associated with rapid (5-30 min) increases in intracellular levels of diradylglycerol. Taken together, these findings demonstrate that the exposure of keratinocytes to ethanol results in the activation of protein kinase C and c-jun expression.
本研究表明,乙醇可诱导人角质形成细胞中c-jun原癌基因的表达。在暴露于1%乙醇1小时时即可检测到c-jun mRNA水平升高,且在24小时时仍高于对照角质形成细胞。在乙醇浓度为0.1%和0.5%时也可检测到c-jun表达增加。对于相关的jun-B和c-fos早期反应基因也获得了类似的结果。结果还表明,乙醇暴露与胞质溶胶和膜组分中蛋白激酶C活性的增加有关。这种增加在5分钟时即可检测到,在30 - 60分钟时达到最大值。乙醇诱导的c-jun表达被异喹啉磺酰胺衍生物H7抑制,但未被HA1004抑制,这一发现表明这种效应是由蛋白激酶C介导的。此外,长时间暴露于12-O-十四烷酰佛波醇-13-乙酸酯导致蛋白激酶C下调,这与乙醇诱导的c-jun表达受阻有关。我们还证明,乙醇暴露与二酰基甘油细胞内水平的快速(5 - 30分钟)升高有关。综上所述,这些发现表明角质形成细胞暴露于乙醇会导致蛋白激酶C的激活和c-jun表达。