The effects of forskolin on adenylate cyclase in S49 wild type and cyc- cells.

R W Downs, G D Aurbach
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Abstract

The effect of forskolin on adenylate cyclase in S49 wild type and cyc- cells was tested. Forskolin stimulated adenylate cyclase activity in cyc- membranes, particularly with Mn++ as cofactor. Forskolin stimulation of adenylate cyclase in wild type membranes was greater than in cyc- membranes, and the ability of forskolin to stimulate cyc- membranes was enhanced by Lubrol PX extracts of human erythrocyte membranes. Compared to its potent effect on intact wild type cells, forskolin was a poor stimulator of cAMP accumulation in cyc- cells. Cyc- cells proliferated in medium containing forskolin, while the growth of wild type cells in such medium was inhibited and the wild type cells ultimately died. Clones selected from a suspension of wild type cells on the basis of forskolin resistance showed the characteristics of cyc- cells. Thus, forskolin does not substantially activate adenylate cyclase activity in intact cyc- cells. Our data indicate that the guanine nucleotide regulatory protein (G/F) enhances forskolin activation of adenylate cyclase.

福斯克林对S49野生型和cyc细胞腺苷酸环化酶的影响。
研究了福斯克林对S49野生型和cyc细胞腺苷酸环化酶的影响。Forskolin刺激环膜腺苷酸环化酶的活性,特别是与Mn++作为辅助因子。福斯可林对野生型细胞膜腺苷酸环化酶的刺激作用大于对cyc-细胞膜的刺激作用,人红细胞膜的Lubrol PX提取物增强了福斯可林对cyc-细胞膜的刺激作用。与其对完整野生型细胞的有效作用相比,forskolin在cyc-细胞中对cAMP积累的刺激作用较差。Cyc-细胞在含forskolin的培养基中增殖,而野生型细胞在含forskolin的培养基中生长受到抑制,最终死亡。从野生型细胞悬浮液中选择的克隆显示出周期细胞的特征。因此,在完整的细胞周期中,福斯克林并不能实质上激活腺苷酸环化酶的活性。我们的数据表明,鸟嘌呤核苷酸调节蛋白(G/F)增强福斯克林活化腺苷酸环化酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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