Wada Taira, Ihunnah Chibueze A, Gao Jie, Chai Xiaojuan, Zeng Su, Philips Brian J, Rubin J Peter, Marra Kacey G, Xie Wen
Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA.
Mol Endocrinol. 2011 Sep;25(9):1612-23. doi: 10.1210/me.2011-1089. Epub 2011 Aug 4.
The estrogen sulfotransferase (EST) is a phase II drug-metabolizing enzyme known to catalyze the sulfoconjugation of estrogens. EST is highly expressed in the white adipose tissue of male mice, but the role of EST in the development and function of adipocytes remains largely unknown. In this report, we showed that EST played an important role in adipocyte differentiation. EST was highly expressed in 3T3-L1 preadipocytes and primary mouse preadipocytes. The expression of EST was dramatically reduced in differentiated 3T3-L1 cells and mature primary adipocytes. Overexpression of EST in 3T3-L1 cells prevented adipocyte differentiation. In contrast, preadipocytes isolated from EST knockout (EST-/-) mice exhibited enhanced differentiation. The inhibitory effect of EST on adipogenesis likely resulted from the sustained activation of ERK1/2 MAPK and inhibition of insulin signaling, leading to a failure of switch from clonal expansion to differentiation. The enzymatic activity of EST was required for the inhibitory effect of EST on adipogenesis, because an enzyme-dead EST mutant failed to inhibit adipocyte differentiation. In vivo, overexpression of EST in the adipose tissue of female transgenic mice resulted in smaller adipocyte size. Taken together, our results suggest that EST functions as a negative regulator of adipogenesis.
雌激素磺基转移酶(EST)是一种已知可催化雌激素硫酸化结合反应的II相药物代谢酶。EST在雄性小鼠的白色脂肪组织中高表达,但EST在脂肪细胞发育和功能中的作用仍 largely unknown。在本报告中,我们表明EST在脂肪细胞分化中起重要作用。EST在3T3-L1前脂肪细胞和原代小鼠前脂肪细胞中高表达。在分化的3T3-L1细胞和成熟的原代脂肪细胞中,EST的表达显著降低。在3T3-L1细胞中过表达EST可阻止脂肪细胞分化。相反,从EST基因敲除(EST-/-)小鼠分离的前脂肪细胞表现出增强的分化。EST对脂肪生成的抑制作用可能是由于ERK1/2 MAPK的持续激活和胰岛素信号传导的抑制,导致从克隆扩增到分化的转换失败。EST对脂肪生成的抑制作用需要EST的酶活性,因为酶失活的EST突变体未能抑制脂肪细胞分化。在体内,雌性转基因小鼠脂肪组织中EST的过表达导致脂肪细胞尺寸变小。综上所述,我们的结果表明EST作为脂肪生成的负调节因子发挥作用。