EGF对甲状腺滤泡cAMP形成的抑制作用是由细胞内ca2 ++介导的。

W. Greil, G. Niedernhuber, D. Stübner, R. Gärtner
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引用次数: 5

摘要

在离体猪甲状腺滤泡中研究了EGF对camp抑制作用的机制。EGF对tsh诱导的camp形成的抑制作用最大可达40%,这种作用持续到孵育前1小时。钙离子载体a23187也能抑制camp的形成,但其作用在1 h后减弱。磷酸酯TPA对camp的形成有双相影响,在持续抑制(60 min)之前有短暂的增加(5 min);二酰基甘油- 1-油基-2-乙酰基-甘油模拟了抑制作用。外源花生四烯酸对camp形成的抑制作用很小且短暂。我们得出结论,EGF通过提高细胞内Ca++以及直接激活蛋白激酶C来抑制camp的形成,这表明磷酸化产物可能是抑制腺苷酸环化酶的介质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of cAMP formation by EGF in thyroid follicles is mediated by intracellular Ca++.
The mechanism of cAMP-inhibition by EGF was studied in isolated porcine thyroid follicles. EGF inhibited TSH-induced cAMP-formation maximally by 40%, this effect remained up to 1 h of pre-incubation. The calcium-ionophore A 23 187 also inhibited cAMP-formation, but its effect was relieved after 1 h. The phorbolester TPA had a biphasic influence on cAMP-formation, with a transient increase (5 min) before a sustained inhibition (60 min); the inhibitory effect was mimicked by the diacylglycerol 1-oleoyl-2-acetyl-glycerol. Exogenous arachidonic acid had only a small and transient inhibitory effect on cAMP-formation. We conclude, that EGF inhibits cAMP-formation by a raise of intracellular Ca++, as well as by the direct activation of proteinkinase C, indicating, that a phosphorylated product could be a mediator for the inhibition of adenylate cyclase.
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