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胰岛素、百日咳毒素和霍乱毒素对3T3成纤维细胞蛋白质合成及二酰基甘油生成的影响:胰岛素信号机制中G蛋白介导的磷脂酶C激活的证据

Effects of insulin, pertussis toxin and cholera toxin on protein synthesis and diacylglycerol production in 3T3 fibroblasts: evidence for a G-protein mediated activation of phospholipase C in the insulin signal mechanism.

作者信息

Hesketh J E, Campbell G P

机构信息

Rowett Research Institute, Bucksburn, Aberdeen.

出版信息

Biosci Rep. 1987 Jul;7(7):533-41. doi: 10.1007/BF01119769.

Abstract

The rapid increase in protein synthesis that occurs on addition of insulin (1 mU/ml) to stepped-down 3T3 cells was blocked by pre-incubation of the cells with pertussis toxin. Cholera toxin on the other hand stimulated protein synthesis and this effect was insensitive to actinomycin D and inhibited by pre-treatment of the cells with phorbol dibutyrate to deplete cell protein kinase C. Insulin was found to cause a rapid and transient increase in diacylglycerol (DAG) synthesis. The insulin-induced increase in diacylglycerol was blocked by pertussis toxin. Exogenous DAG (10 microM) stimulated protein synthesis within 1 hour. The results suggest that insulin stimulates ribosomal activity through a signal mechanism that involves a G-protein mediated activation of phospholipase C to increase DAG levels.

摘要

向逐步传代的3T3细胞中添加胰岛素(1 mU/ml)后,蛋白质合成迅速增加,而这种增加在细胞预先用百日咳毒素孵育后被阻断。另一方面,霍乱毒素刺激蛋白质合成,且这种效应不受放线菌素D的影响,并且在用佛波醇二丁酸酯预处理细胞以耗尽细胞蛋白激酶C后受到抑制。发现胰岛素会导致二酰基甘油(DAG)合成迅速且短暂地增加。胰岛素诱导的二酰基甘油增加被百日咳毒素阻断。外源性DAG(10 microM)在1小时内刺激蛋白质合成。结果表明,胰岛素通过一种信号机制刺激核糖体活性,该机制涉及G蛋白介导的磷脂酶C激活以增加DAG水平。

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