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下丘脑前阿黑皮素原神经元中 Sirtuin 6 的超生理过表达通过下丘脑-脂肪轴促进肥胖。

Sirtuin 6 supra-physiological overexpression in hypothalamic pro-opiomelanocortin neurons promotes obesity via the hypothalamus-adipose axis.

机构信息

Laboratory of Clinical Pharmacy and Adverse Drug Reaction, West China Hospital of Sichuan University, Chengdu, China.

Department of Pharmacy, West China Hospital of Sichuan University, Chengdu, China.

出版信息

FASEB J. 2021 Mar;35(3):e21408. doi: 10.1096/fj.202002607.

Abstract

Sirtuin 6 (Sirt6), a member of the Sirtuin family, has important roles in maintaining glucose and lipid metabolism. Our previous studies demonstrated that the deletion of Sirt6 in pro-opiomelanocortin (POMC)-expressing cells by the loxP-Cre system resulted in severe obesity and hepatic steatosis. However, whether overexpression of Sirt6 in hypothalamic POMC neurons could ameliorate diet-induced obesity is still unknown. Thus, we generated mice specifically overexpressing Sirt6 in hypothalamic POMC neurons (PSOE) by stereotaxic injection of Cre-dependent adeno-associated viruses into the arcuate nucleus of Pomc-Cre mice. PSOE mice showed increased adiposity and decreased energy expenditure. Furthermore, thermogenesis of BAT and lipolysis of WAT were both impaired, caused by reduced sympathetic nerve innervation and activity in adipose tissues. Mechanistically, Sirt6 overexpression decreasing STAT3 acetylation, thus lowering POMC expression in the hypothalamus underlined the observed phenotypes in PSOE mice. These results demonstrate that Sirt6 overexpression specifically in the hypothalamic POMC neurons exacerbates diet-induced obesity and metabolic disorders via the hypothalamus-adipose axis.

摘要

Sirtuin 6(Sirt6)是 Sirtuin 家族的一员,在维持葡萄糖和脂质代谢方面发挥着重要作用。我们之前的研究表明,通过 loxP-Cre 系统在表达 pro-opiomelanocortin(POMC)的细胞中敲除 Sirt6 会导致严重的肥胖和肝脂肪变性。然而,Sirt6 在下丘脑 POMC 神经元中的过表达是否能改善饮食诱导的肥胖仍然未知。因此,我们通过立体定位注射 Cre 依赖性腺相关病毒到 Pomc-Cre 小鼠的弓状核中,特异性地在下丘脑 POMC 神经元中过表达 Sirt6 生成了 PSOE 小鼠。PSOE 小鼠表现出肥胖增加和能量消耗减少。此外,脂肪组织中交感神经支配和活性减少导致 BAT 的产热和 WAT 的脂肪分解都受损。从机制上讲,Sirt6 过表达降低 STAT3 乙酰化,从而降低了下丘脑 POMC 的表达,这解释了 PSOE 小鼠的表型。这些结果表明,Sirt6 在下丘脑 POMC 神经元中的特异性过表达通过下丘脑-脂肪轴加剧了饮食诱导的肥胖和代谢紊乱。

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