Chrétien Aline, Dierick Jean-François, Delaive Edouard, Larsen Martin Røssel, Dieu Marc, Raes Martine, Deroanne Christophe F, Roepstorff Peter, Toussaint Olivier
Research Unit on Cellular Biology, University of Namur, B-5000 Namur, Belgium.
Free Radic Biol Med. 2008 May 1;44(9):1732-51. doi: 10.1016/j.freeradbiomed.2008.01.026. Epub 2008 Feb 12.
The role of TGF-beta1 in hydrogen peroxide-induced senescence-like morphogenesis has been described. The aim of this work was to investigate whether TGF-beta1-independent changes in protein synthesis are involved in this morphogenesis and to study possible mechanisms occurring earlier than TGF-beta1 overexpression. Among the multiple TGF-beta1-independent changes in protein neosynthesis, followed or not by posttranslational modifications, identified by proteomic analysis herein, those of ezrin, L-caldesmon, and HSP27 were particularly studied. Rho-GTPase cdc42 was shown to be responsible for p38(MAPK) activation, in turn triggering phosphorylation of L-caldesmon and HSP27. Cdc42 was also shown to be mainly responsible for the increase in TGF-beta1 mRNA level observed at 24 h after treatment with H(2)O(2) and onward. This study further clarified the mechanisms of senescence-like morphogenesis in addition to the previously demonstrated role of TGF-beta1 signaling pathways.
TGF-β1在过氧化氢诱导的衰老样形态发生中的作用已被描述。本研究的目的是调查蛋白质合成中不依赖TGF-β1的变化是否参与这种形态发生,并研究比TGF-β1过表达更早发生的可能机制。在本文通过蛋白质组学分析确定的蛋白质新合成中多种不依赖TGF-β1的变化(无论是否伴随翻译后修饰)中,尤其研究了埃兹蛋白、L-钙调蛋白和热休克蛋白27(HSP27)的变化。Rho-GTP酶cdc42被证明是p38(丝裂原活化蛋白激酶)激活的原因,进而引发L-钙调蛋白和HSP27的磷酸化。Cdc42还被证明主要是过氧化氢(H₂O₂)处理24小时及之后观察到的TGF-β1 mRNA水平升高的原因。除了先前证明的TGF-β1信号通路的作用外,本研究进一步阐明了衰老样形态发生的机制。