Departamento de Biología Celular y Desarrollo, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Ap. Postal 70-248, México D.F. 04510.
Eur J Pharmacol. 2010 Dec 1;648(1-3):1-5. doi: 10.1016/j.ejphar.2010.08.049. Epub 2010 Sep 7.
Receptor tyrosine kinases and G protein-coupled receptors modulate physiological processes and are also involved in the pathogenesis of some diseases. These receptors have intense bidirectional crosstalks leading to interactions in their signaling pathways and also modulation of the receptors themselves. In some cases, the receptor tyrosine kinases phosphorylate G protein-coupled receptors whereas in others phosphoinositide 3-kinase, protein kinase B and protein kinase C are key elements in these crosstalks. Two paracrine/ autocrine processes also participate, i.e., epidermal growth factor transactivation and sphingosine 1-phosphate generation and signaling. G proteins seem to mediate actions of receptor tyrosine kinases, but how this takes place is far from completely understood; some models are presented. Recent data indicate that the mitogen activated protein kinase cascade also mediate crosstalks. In the present perspective these processes are outlined using information from receptors that have been intensively studied, and important gaps in our knowledge are indicated.
受体酪氨酸激酶和 G 蛋白偶联受体调节生理过程,也参与一些疾病的发病机制。这些受体具有强烈的双向串扰,导致信号通路中的相互作用以及受体本身的调节。在某些情况下,受体酪氨酸激酶磷酸化 G 蛋白偶联受体,而在其他情况下,磷酸肌醇 3-激酶、蛋白激酶 B 和蛋白激酶 C 是这些串扰中的关键因素。两种旁分泌/自分泌过程也参与其中,即表皮生长因子的转激活和鞘氨醇 1-磷酸的产生和信号转导。G 蛋白似乎介导受体酪氨酸激酶的作用,但这是如何发生的还远未完全了解;提出了一些模型。最近的数据表明,丝裂原活化蛋白激酶级联也介导串扰。在本研究中,使用已经深入研究的受体的信息概述了这些过程,并指出了我们知识中的重要空白。