Wu Rong, Liu Xiao-Meng, Sun Jian-Guang, Chen Hong, Ma Jun, Dong Meng, Peng Shengyi, Wang Ji-Qiu, Ding Jian-Qing, Li Dong-Hao, Speakman John R, Ning Guang, Jin Wanzhu, Yuan Zengqiang
State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.
Key Laboratory of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China; College of life science and agronomy, Zhoukou Normal University, Zhoukou, China.
Cell Discov. 2017 Feb 14;3:16054. doi: 10.1038/celldisc.2016.54. eCollection 2017.
DJ-1 protein is involved in multiple physiological processes, including Parkinson's disease. However, the role of DJ-1 in the metabolism is largely unknown. Here we found that DJ-1 maintained energy balance and glucose homeostasisvia regulating brown adipose tissue (BAT) activity. DJ-1-deficient mice reduced body mass, increased energy expenditure and improved insulin sensitivity. DJ-1 deletion also resisted high-fat-diet (HFD) induced obesity and insulin resistance. Accordingly, DJ-1 transgene triggered autonomous obesity and glucose intolerance. Further BAT transplantation experiments clarified DJ-1 regulates energy and glucose homeostasis by modulating BAT function. Mechanistically, we found that DJ-1 promoted PTEN proteasomal degradation via an E3 ligase, mind bomb-2 (Mib2), which led to Akt activation and inhibited FoxO1-dependent Ucp1 (Uncoupling protein-1) expression in BAT. Consistently, ablation of Akt1 mitigated the obesity and BAT dysfunction induced by DJ-1 transgene. These findings define a new biological role of DJ-1 protein in regulating BAT function, with an implication of the therapeutic target in the treatment of metabolic disorders.
DJ-1蛋白参与多种生理过程,包括帕金森病。然而,DJ-1在新陈代谢中的作用在很大程度上尚不清楚。在此我们发现,DJ-1通过调节棕色脂肪组织(BAT)的活性来维持能量平衡和葡萄糖稳态。DJ-1基因缺陷小鼠体重减轻、能量消耗增加且胰岛素敏感性提高。DJ-1缺失还能抵抗高脂饮食(HFD)诱导的肥胖和胰岛素抵抗。相应地,DJ-1转基因引发了自发性肥胖和葡萄糖不耐受。进一步的BAT移植实验表明,DJ-1通过调节BAT功能来调控能量和葡萄糖稳态。从机制上来说,我们发现DJ-1通过一种E3连接酶mind bomb-2(Mib2)促进PTEN的蛋白酶体降解,这导致Akt激活并抑制BAT中FoxO1依赖的Ucp1(解偶联蛋白-1)表达。同样,敲除Akt1可减轻DJ-1转基因诱导的肥胖和BAT功能障碍。这些发现确定了DJ-1蛋白在调节BAT功能方面的新生物学作用,这对代谢紊乱治疗中的治疗靶点具有启示意义。