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Protein scaffolds in MAP kinase signalling
被引:169
作者:
Brown, Matthew D.
Sacks, David B.
[1
]
机构:
[1] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
基金:
美国国家卫生研究院;
关键词:
MAPK;
Scaffolds;
Cancer;
Compartmentalisation;
GROWTH-FACTOR RECEPTOR;
CELL-ADHESION;
E-CADHERIN;
IQGAP1;
RAS;
ACTIVATION;
ERK;
LOCALIZATION;
SPECIFICITY;
ENDOCYTOSIS;
D O I:
10.1016/j.cellsig.2008.11.013
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The mitogen-activated protein kinase (MAPK) pathway allows cells to interpret external signals and respond in an appropriate way. Diverse cellular functions, ranging from differentiation and proliferation to migration and inflammation, are regulated by MAPK signalling. Therefore, cells have developed mechanisms by which this single pathway modulates numerous cellular responses from a wide range of activating factors. This specificity is achieved by several mechanisms, including temporal and spatial control of MAPK signalling components. Key to this control are protein scaffolds, which are multidomain proteins that interact with components of the MAPK cascade in order to assemble signalling complexes. Studies conducted on different scaffolds, in different biological systems, have shown that scaffolds exert substantial control over MAPK signalling, influencing the signal intensity. time course and, importantly, the cellular responses. Protein scaffolds, therefore, are integral elements to the modulation of the MAPK network in fundamental physiological processes. (C) 2008 Elsevier Inc. All rights reserved.
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页码:462 / 469
页数:8
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