Regulation of mitogen-activated protein kinase pathways by the plasma membrane Na+/H+ exchanger, NHE1

被引:42
作者
Pedersen, Stine Falsig [1 ]
Darborg, Barbara Vasek [1 ]
Rentsch, Maria Louise [1 ]
Rasmussen, Maria [1 ]
机构
[1] Univ Copenhagen, Dept Mol Biol, DK-2100 Copenhagen, Denmark
关键词
JNK; ERK; p38; MAPK; intracellular pH; intracellular sodium concentration; scaffold; cell volume regulation; osmotic stress; ischemia; hypertrophy; SIGNAL-TRANSDUCTION PATHWAYS; PHOSPHATASE MKP-1; CELL SHRINKAGE; ERM PROTEINS; MAP KINASES; P38; MAPK; STRESS; ISOFORM-1; CASCADE; GROWTH;
D O I
10.1016/j.abb.2006.12.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mitogen-activated protein kinases (MAPKs), including extracellular signal-regulated kinase (ERK), e-Jun N-terminal kinase (JNK), and p38 MAPK, play a major role in the regulation of pivotal cellular processes such as cell death/survival balance, cell cycle progression, and cell migration. MAPK activity is regulated by a three-tiered phosphorelay system, which is in turn regulated by a complex network of signaling events and scaffolding proteins. The ubiquitous plasma membrane Na+/H+ exchanger NHE1 is activated by, and implicated in, the physiological/pathophysiologicaI responses to many of the same stimuli that modulate MAPK activity. While under some conditions, NHE1 is regulated by MAPKs, a number of studies have, conversely, implicated NHE1 in the regulation of MAPK activity. Here, we discuss the current evidence indicating the involvement of NHE1] in MAPK regulation, the mechanisms by which this may occur, and the possible physiological and pathophysiological relevance of this phenomenon. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:195 / 201
页数:7
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