Khor Victor K, Tong Ming Han, Qian Yueming, Song Wen-Chao
Department of Pharmacology and Institute for Translational Medicine and Therapeutics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Endocrinology. 2008 Nov;149(11):5440-8. doi: 10.1210/en.2008-0271. Epub 2008 Jul 31.
Although primarily regarded as a sex steroid, estrogen plays an important role in many other physiological processes including adipose development and disposition. Estrogen sulfotransferase (EST) regulates estrogen activity by catalyzing the sulfoconjugation and inactivation of estrogens. In the present study, we report the gender-specific expression of EST in adipose tissues of the mouse and describe contrasting mechanisms of EST regulation in the fat and liver. EST is expressed in the white adipose tissues of the male but not female mouse. Within the various fat depots of male mice, it is most abundantly expressed in the epididymal fat pad, with variable levels in other white fats and no expression in the brown fat. Fractionation of epididymal fat cells showed EST to be predominantly associated with stromal vascular cells (preadipocyte). EST expression in male mouse adipose tissues is dependent on testosterone as castration ablated, and administration of exogenous testosterone restored, EST expression. Furthermore, testosterone treatment induced abnormal EST expression in the parametrial fat of female mice. EST induction by testosterone in female mice is tissue specific because testosterone treatment had no effect on liver EST expression. Conversely, the liver X receptor agonist TO-901317 induced EST expression in female mouse liver but not in their adipose tissues. Finally, we demonstrate that male EST knockout mice developed increased epididymal fat accumulation with enlarged adipocyte size. We conclude that EST is expressed in adipose tissues in a sexually dimorphic manner, is regulated by testosterone, and plays a physiological role in regulating adipose tissue accumulation in male mice.
尽管雌激素主要被视为一种性类固醇,但它在许多其他生理过程中发挥着重要作用,包括脂肪的发育和分布。雌激素磺基转移酶(EST)通过催化雌激素的硫酸化结合和失活来调节雌激素活性。在本研究中,我们报告了EST在小鼠脂肪组织中的性别特异性表达,并描述了其在脂肪和肝脏中不同的调节机制。EST在雄性小鼠而非雌性小鼠的白色脂肪组织中表达。在雄性小鼠的各种脂肪库中,它在附睾脂肪垫中表达最为丰富,在其他白色脂肪中的表达水平各异,而在棕色脂肪中不表达。对附睾脂肪细胞进行分级分离显示,EST主要与基质血管细胞(前脂肪细胞)相关。雄性小鼠脂肪组织中的EST表达依赖于睾酮,因为去势会消除EST表达,而给予外源性睾酮可恢复其表达。此外,睾酮处理可诱导雌性小鼠子宫旁脂肪中EST异常表达。睾酮对雌性小鼠EST的诱导具有组织特异性,因为睾酮处理对肝脏EST表达没有影响。相反,肝脏X受体激动剂TO-901317可诱导雌性小鼠肝脏而非其脂肪组织中的EST表达。最后,我们证明雄性EST基因敲除小鼠的附睾脂肪积累增加,脂肪细胞大小增大。我们得出结论,EST在脂肪组织中以性别二态性方式表达,受睾酮调节,并在调节雄性小鼠脂肪组织积累中发挥生理作用。