Seven-transmembrane receptor signalling and ERK compartmentalization

被引:65
作者
Caunt, Christopher J. [1 ]
Finch, Ann R. [1 ]
Sedgley, Kathleen R. [1 ]
McArdle, Craig A. [1 ]
机构
[1] Univ Bristol, Henry Wellcome Labs Integrat Neurosci & Endocrino, Bristol BS1 3NY, Avon, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.tem.2006.07.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vast numbers of extracellular signalling molecules exert effects on their target cells by activation of a relatively limited number of mitogen-activated protein kinase (MAPK) cascades, raising the question of how specificity is achieved. To a large extent, this appears to be attributable to differences in kinetics and compartmentalization of MAPK protein activation that are dictated by MAPK-associated proteins serving as scaffolds, anchors, activators or effectors. Here, we review spatiotemporal aspects of signalling via the Ras-Raf-extracellular signal-regulated kinase pathway, emphasizing recent work on roles of arrestins as scaffolds and transducers for seven transmembrane receptor signalling.
引用
收藏
页码:276 / 283
页数:8
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