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G蛋白偶联受体与调节生长反应的信号通路。

G protein-coupled receptors and signaling pathways regulating growth responses.

作者信息

Post G R, Brown J H

机构信息

Department of Pharmacology, University of California, San Diego, La Jolla 92093, USA.

出版信息

FASEB J. 1996 May;10(7):741-9. doi: 10.1096/fasebj.10.7.8635691.

Abstract

Hormones that interact with seven-transmembrane spanning receptors, generally considered to be involved in acute signaling functions, also induce longer term effects on gene expression and cell growth. These genetic and proliferative effects can be induced by activation of receptors that signal through heterotrimeric GTP-binding proteins (G-proteins) of the Gq family, pertussis toxin-sensitive Gi/Go proteins, Gs, or G12/G13. Numerous growth-promoting G protein-coupled receptors activate the low molecular weight G-protein Ras and stimulate mitogen-activated protein kinase. Recent data suggest that c-Jun NH2-terminal kinase is also activated, possibly through interaction with low molecular weight G-proteins of the Rho family. Because G protein-coupled receptors lack intrinsic tyrosine kinase activity, the mechanisms by which heterotrimeric G-proteins couple to these kinase cascades remain to be elucidated. By analogy to growth factor receptors, G protein-coupled receptors may access these kinase cascades through binding of adapter proteins or recruitment of cytosolic tyrosine kinases. It is likely that interactions between multiple signaling pathways are required for G protein-coupled receptors to propagate signals to the nucleus.

摘要

通常认为与七次跨膜受体相互作用的激素参与急性信号传导功能,它们也会对基因表达和细胞生长产生更长期的影响。这些遗传和增殖效应可由通过Gq家族的异三聚体GTP结合蛋白(G蛋白)、百日咳毒素敏感的Gi/Go蛋白、Gs或G12/G13发出信号的受体激活所诱导。许多促进生长的G蛋白偶联受体激活低分子量G蛋白Ras并刺激丝裂原活化蛋白激酶。最近的数据表明,c-Jun氨基末端激酶也可能通过与Rho家族的低分子量G蛋白相互作用而被激活。由于G蛋白偶联受体缺乏内在的酪氨酸激酶活性,异三聚体G蛋白与这些激酶级联反应偶联的机制仍有待阐明。与生长因子受体类似,G蛋白偶联受体可能通过衔接蛋白的结合或胞质酪氨酸激酶的募集来接入这些激酶级联反应。G蛋白偶联受体可能需要多个信号通路之间的相互作用才能将信号传递至细胞核。

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