The small Rho GTPase Rac1 controls normal human dermal fibroblasts proliferation with phosphorylation of the oncoprotein c-myc

被引:7
作者
Nikolova, Ekaterina
Mitev, Vanio
Zhelev, Nikolal
Deroanne, Christophe F.
Poumay, Yves [1 ]
机构
[1] Univ Namur, URPHYM, Cell & Tissue Lab, FUNDP, B-5000 Namur, Belgium
[2] Med Univ Sofia, Dept Chem & Biochem, Sofia 1431, Bulgaria
[3] Univ Abertay, Sch Contemporary Sci, Dundee, Scotland
[4] Univ Liege, GBIG GIGA Res Ctr, Lab Connect Tissues Biol, B-4000 Sart Tilman Par Liege, Belgium
关键词
normal human skin fibroblasts; Rac1; phospho-ERK1/2; phospho-p38; phospho-c-myc; proliferation;
D O I
10.1016/j.bbrc.2007.05.214
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
Proliferation of dermal fibroblasts is crucial for the maintenance of skin. The small Rho GTPase, Rac1, has been identified as a key transducer of proliferative signals in various cell types, but in normal human dermal fibroblasts its significance to cell growth control has not been studied. In this study, we applied the method of RNA interference to suppress endogenous Rac1 expression and examined the consequences on human skin fibroblasts. Rac1 knock-down resulted in inhibition of DNA synthesis. This effect was not mediated by inhibition of the central transducer of proliferative stimuli, ERK1/2 or by activation of the pro-apoptotic p38. Rather, as a consequence of the suppressed Racl expression we observed a significant decrease in phosphorylation of c-myc, revealing for the first time that in human fibroblasts Rac1 exerts control on proliferation through c-myc phosphorylation. Thus Rac1 activates proliferation of normal fibroblasts through stimulation of c-myc phosphorylation without affecting ERK1/2 activity. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:834 / 839
页数:6
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