Qin Haojie, Zhong Yi, Huang Jinhui, Miao Yanli, Du Meng, Huang Kai
Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Adv Sci (Weinh). 2025 Apr;12(13):e2414073. doi: 10.1002/advs.202414073. Epub 2025 Feb 10.
In mammals, the activation of thermogenic adipocytes, such as beige and brown adipocytes, can significantly increase overall energy expenditure, offering a promising strategy to combat metabolic diseases. Despite its considerable potential, the regulatory mechanisms governing this activation remain largely elusive. This study bridges this gap by elucidating that tripartite motif 56 (TRIM56), an E3 ubiquitin ligase, is upregulated in response to cold stimuli, thereby promoting the recruitment of beige adipocytes. Notably, the overexpression of TRIM56 in adipocytes is shown to help mice maintain a core temperature under cold conditions, as well as confer protection against diet-induced obesity. Mechanistically, TRIM56 facilitates the degradation of the transducin-like enhancer protein 3 (TLE3) protein by promoting its K48-linked ubiquitination, which subsequently triggers the activation of thermogenic genes in subcutaneousl white adipose tissue and improved the metabolic profiles. These findings unveil a novel function for TRIM56 in adipocyte browning, suggesting its potential as a therapeutic target for the treatment of metabolic disorders.
在哺乳动物中,产热脂肪细胞(如米色和棕色脂肪细胞)的激活可显著增加总体能量消耗,为对抗代谢性疾病提供了一种有前景的策略。尽管其潜力巨大,但控制这种激活的调节机制在很大程度上仍不清楚。本研究通过阐明E3泛素连接酶三聚体基序56(TRIM56)在冷刺激下上调,从而促进米色脂肪细胞的募集,填补了这一空白。值得注意的是,脂肪细胞中TRIM56的过表达被证明有助于小鼠在寒冷条件下维持核心体温,并对饮食诱导的肥胖提供保护。机制上,TRIM56通过促进转导素样增强子蛋白3(TLE3)的K48连接的泛素化来促进其蛋白质降解,随后触发皮下白色脂肪组织中产热基因的激活并改善代谢状况。这些发现揭示了TRIM56在脂肪细胞棕色化中的新功能,表明其作为治疗代谢紊乱的治疗靶点的潜力。