Regulation of mitogen-activated protein kinases in cardiac myocytes through the small G protein Rac1

被引:128
作者
Clerk, A
Pham, FH
Fuller, SJ
Sahai, E
Aktories, K
Marais, R
Marshall, C
Sugden, PH
机构
[1] Imperial Coll Sch Med, Div Biomed Sci, Mol Pathol Sect, London SW7 2AZ, England
[2] Imperial Coll Sch Med, NHLI Div, Cardiac Med Sect, London SW3 6LY, England
[3] Inst Canc Res, Chester Beatty Labs, London SW3 6JB, England
[4] Univ Freiburg, Inst Pharmakol & Toxikol, D-79104 Freiburg, Germany
关键词
D O I
10.1128/MCB.21.4.1173-1184.2001
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
Small guanine nucleotide-binding proteins of the Ras and Rho (Rac, Cdc42, and Rho) families have been implicated in cardiac myocyte hypertrophy, and this may involve the extracellular signal-related kinase (ERK), c-Jun N-terminal kinase (NK), and/or p38 mitogen-activated protein kinase (MAPK) cascades. In other systems, Rac and Cdc42 have been particularly implicated in the activation of JNKs and p38-MAPKs. We examined the activation of Rho family small G proteins and the regulation of MAPKs through Rad in cardiac myocytes, Endothelin 1 and phenylephrine (both hypertrophic agonists) induced rapid activation of endogenous Rad, and endothelin 1 also promoted significant activation of RhoA, Toxin B (which inactivates Rho Family proteins) attenuated the activation of JNKs by hyperosmotic shock or endothelin 1 but had no effect on p38-MAPK activation. Toxin B also inhibited the activation of the ERK cascade by these stimuli. Tn transfection experiments, dominant-negative N17Rac1 inhibited activation of ERK by endothelin 1, whereas activated V12Rac1 cooperated with c-RaF to activate ERK, Rac1 may stimulate the ERK cascade either by promoting the phosphorylation of c-Raf or by increasing MEK1 and/or -2 association with c-Raf to facilitate MEK1 and/or -2 activation. In cardiac myocytes, toxin B attenuated c-Raf(Ser-338) phosphorylation (50 to 70% inhibition), but this had no effect on c-Raf activity. However, toxin B decreased both the association of MEK1 and/or -2 with c-Raf and c-Raf-associated ERK-activating activity. V12Rac1 cooperated with c-Raf to increase expression of atrial natriuretic factor (ANF), whereas N17Rac1 inhibited endothelin 1-stimulated ANF expression, indicating that the synergy between Rad and c-Raf is potentially physiologically important. We conclude that activation of Rad by hypertrophic stimuli contributes to the hypertrophic response by modulating the ERK and/or possibly the JNK (but not the p38-MAPK) cascades.
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页码:1173 / 1184
页数:12
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