Choe Hun Jee, Lee Ji Seon, Park Jong Yoen, Lee Seung-Ah, Park Young Joo, Chung Sung Soo, Park Kyong Soo
Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Department of Internal Medicine, Hallym University Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Republic of Korea.
Exp Mol Med. 2025 Jun;57(6):1283-1293. doi: 10.1038/s12276-025-01458-5. Epub 2025 Jun 27.
Brown adipose tissue (BAT) is responsible for energy homeostasis and adaptive thermogenesis. SUMO-specific protease 2 (SENP2) plays an essential role in adipogenesis; however, the role of SENP2 in BAT metabolism has not been explored. Here we investigated the role of SENP2 in mature brown adipocytes with a brown adipocyte-specific SENP2 knockout (Senp2-BKO) mouse model generated using the uncoupling protein 1 (Ucp1)-Cre. High-fat diet-induced insulin resistance was aggravated in Senp2-BKO mice compared with control mice. In Senp2-BKO mice, adaptive thermogenesis upon acute cold exposure was impaired and UCP1 expression was barely induced upon cold or β-adrenergic stimulation. SENP2-mediated deSUMOylation of estrogen-related receptor alpha (ERRα) significantly enhanced Ucp1 promoter activity through activation of the ERRα/PGC1α complex. The absence of SENP2 inhibited formation of ERRα, cAMP-response element-binding protein (CREB) and RNA Polymerase II transcriptional complex at the Ucp1 promoter following β3-adrenergic stimulation. In addition, SUMOylation of ERRα severely interfered with binding of ERRα to its DNA-binding site (ERRE) in the promoter of Ucp1. Our findings revealed that SENP2 plays a role in the metabolic flexibility and thermogenic efficiency of BAT, particularly in response to β3-adrenergic activation.
棕色脂肪组织(BAT)负责能量稳态和适应性产热。小泛素样修饰特异性蛋白酶2(SENP2)在脂肪生成中起重要作用;然而,SENP2在BAT代谢中的作用尚未得到探索。在这里,我们使用解偶联蛋白1(Ucp1)-Cre构建的棕色脂肪细胞特异性SENP2基因敲除(Senp2-BKO)小鼠模型,研究了SENP2在成熟棕色脂肪细胞中的作用。与对照小鼠相比,高脂饮食诱导的胰岛素抵抗在Senp2-BKO小鼠中加重。在Senp2-BKO小鼠中,急性冷暴露后的适应性产热受损,冷刺激或β-肾上腺素能刺激后UCP1表达几乎未被诱导。SENP2介导的雌激素相关受体α(ERRα)去SUMO化通过激活ERRα/PGC1α复合物显著增强Ucp1启动子活性。缺乏SENP2抑制了β3-肾上腺素能刺激后Ucp1启动子处ERRα、环磷酸腺苷反应元件结合蛋白(CREB)和RNA聚合酶II转录复合物的形成。此外,ERRα的SUMO化严重干扰了ERRα与其在Ucp1启动子中的DNA结合位点(ERRE)的结合。我们的研究结果表明,SENP2在BAT的代谢灵活性和产热效率中发挥作用,特别是在对β3-肾上腺素能激活的反应中。