Dissecting how receptor tyrosine kinases modulate G protein-coupled receptor function

被引:21
作者
Adolfo Garcia-Sainz, J. [1 ]
Teresa Romero-Avila, M. [1 ]
del Carmen Medina, Luz [2 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Fisiol Celular, Dept Biol Celular & Desarrollo, Mexico City 04510, DF, Mexico
[2] Univ Autonoma Metropolitana Iztapalapa, Dept Reprod Biol, Div CBS, Mexico City 09340, DF, Mexico
关键词
G protein-coupled receptors; Receptor tyrosine kinase; Crosstalk; Desensitization; Receptor phosphorylation; GROWTH-FACTOR-I; AGONIST-DEPENDENT MODULATION; G-BETA-GAMMA; ALPHA(1B)-ADRENERGIC RECEPTOR; BETA(2)-ADRENERGIC RECEPTOR; INSULIN-RECEPTOR; MAMMALIAN-CELLS; OPIOID RECEPTOR; EGF RECEPTOR; PHOSPHORYLATION;
D O I
10.1016/j.ejphar.2010.08.049
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
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