Department of Biochemistry, Kindai University Faculty of Medicine, Osaka-Sayama, Osaka, Japan.
Department of Molecular Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Sci Rep. 2019 Jul 11;9(1):10036. doi: 10.1038/s41598-019-46445-9.
Obesity increases the risk of metabolic disorders like diabetes mellitus and dyslipidemia. However, how metabolic status is sensed and regulates cellular behavior is unclear. Utx is an H3K27 demethylase that influences adipocyte function in vitro. To examine its role in vivo, we generated mice lacking Utx in adipocytes (UtxAKO). Although all UtxAKO mice grew normally on a normal chow diet (NCD), female UtxAKO mice on a high fat diet (HFD) showed striking reductions in body fat compared to control mice (Ctrl). Gene expression profiling of adipose tissues of HFD-fed UtxAKO female mice revealed decreased expression of rate-limiting enzymes of triacylglycerol synthesis but increased expression of those of cholesterol/steroid hormone synthesis. Moreover, these animals resisted adiposity induced by ovariectomy and exhibited increased estrogen in visceral adipose tissues. Thus, upon HFD feeding, Utx regulates lipid metabolism in adipose tissues by influencing the local hormonal microenvironment. Conversely, Utx deficiency skews lipid catabolism to enhance cholesterol/steroid hormone production and repress obesity.
肥胖增加了代谢紊乱的风险,如糖尿病和血脂异常。然而,代谢状态是如何被感知和调节细胞行为的还不清楚。UTX 是一种 H3K27 去甲基化酶,它影响体外脂肪细胞的功能。为了研究其在体内的作用,我们生成了脂肪细胞中缺乏 UTX 的小鼠(UTxAKO)。尽管所有 UtxAKO 小鼠在正常饮食(NCD)下正常生长,但高脂肪饮食(HFD)喂养的雌性 UtxAKO 小鼠与对照组相比,体脂明显减少。对高脂肪饮食喂养的 UtxAKO 雌性小鼠脂肪组织的基因表达谱分析显示,三酰甘油合成的限速酶表达降低,但胆固醇/类固醇激素合成的限速酶表达增加。此外,这些动物抵抗了卵巢切除引起的肥胖,并表现出内脏脂肪组织中雌激素增加。因此,在高脂肪饮食喂养下,UTX 通过影响局部激素微环境来调节脂肪组织中的脂质代谢。相反,UTX 缺乏会使脂质分解代谢偏向于增强胆固醇/类固醇激素的产生,并抑制肥胖。