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SENP2 通过 SUMO 特异性蛋白酶控制脂肪生成。

Control of adipogenesis by the SUMO-specific protease SENP2.

机构信息

Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, and Department of Internal Medicine, College of Medicine, Seoul National University, 28 Yongon-dong, Chongno-gu, Seoul 110-744, South Korea.

出版信息

Mol Cell Biol. 2010 May;30(9):2135-46. doi: 10.1128/MCB.00852-09. Epub 2010 Mar 1.

Abstract

Here, we demonstrate that SENP2, a desumoylating enzyme, plays a critical role in the control of adipogenesis. SENP2 expression was markedly increased upon the induction of adipocyte differentiation, and this increase was dependent on protein kinase A activation. Remarkably, knockdown of SENP2 led to a dramatic attenuation of adipogenesis with a marked decrease in PPARgamma and C/EBPalpha mRNA levels. Knockdown of SENP2 also caused a marked reduction in the level of C/EBPbeta protein but not in that of C/EBPbeta mRNA. Interestingly, sumoylation of C/EBPbeta dramatically increased its ubiquitination and destabilization, and this increase could be reversed by SENP2. In addition, overexpression of C/EBPbeta could overcome the inhibitory effect of SENP2 knockdown on adipogenesis. Furthermore, SENP2 was absolutely required for adipogenesis of preadipocytes implanted into mice. These results establish a critical role for SENP2 in the regulation of adipogenesis by desumoylation and stabilization of C/EBPbeta and in turn by promoting the expression of its downstream effectors, such as PPARgamma and C/EBPalpha.

摘要

在这里,我们证明 SENP2(去 SUMO 酶)在脂肪生成的调控中起着关键作用。在诱导脂肪细胞分化时,SENP2 的表达明显增加,而这种增加依赖于蛋白激酶 A 的激活。值得注意的是,SENP2 的敲低导致脂肪生成显著减弱,PPARγ 和 C/EBPα mRNA 水平明显降低。SENP2 的敲低还导致 C/EBPβ 蛋白水平显著降低,但 C/EBPβ mRNA 水平没有降低。有趣的是,C/EBPβ 的 SUMO 化显著增加了其泛素化和不稳定性,而这种增加可以被 SENP2 逆转。此外,C/EBPβ 的过表达可以克服 SENP2 敲低对脂肪生成的抑制作用。此外,SENP2 对于植入小鼠的前脂肪细胞的脂肪生成是绝对必需的。这些结果确立了 SENP2 通过去 SUMO 化和稳定 C/EBPβ 以及反过来通过促进其下游效应物(如 PPARγ 和 C/EBPα)的表达,在调节脂肪生成中起着关键作用。

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