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