School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan, 44919, Republic of Korea.
Obesity Research Center, College of Medicine, King Saud University, Riyadh, 11461, Saudi Arabia.
Nat Commun. 2019 Aug 6;10(1):3536. doi: 10.1038/s41467-019-11302-w.
Tonicity-responsive enhancer binding protein (TonEBP or NFAT5) is a regulator of cellular adaptation to hypertonicity, macrophage activation and T-cell development. Here we report that TonEBP is an epigenetic regulator of thermogenesis and obesity. In mouse subcutaneous adipocytes, TonEBP expression increases > 50-fold in response to high-fat diet (HFD) feeding. Mice with TonEBP haplo-deficiency or adipocyte-specific TonEBP deficiency are resistant to HFD-induced obesity and metabolic defects (hyperglycemia, hyperlipidemia, and hyperinsulinemia). They also display increased oxygen consumption, resistance to hypothermia, and beiging of subcutaneous fat tissues. TonEBP suppresses the promoter of β3-adrenoreceptor gene, a critical regulator of lipolysis and thermogenesis, in ex vivo and cultured adipocytes. This involves recruitment of DNMT1 DNA methylase and methylation of the promoter. In human subcutaneous adipocytes TonEBP expression displays a correlation with body mass index but an inverse correlation with β3-adrenoreceptor expression. Thus, TonEBP is an attractive therapeutic target for obesity, insulin resistance, and hyperlipidemia.
张力反应增强结合蛋白(TonEBP 或 NFAT5)是细胞适应高渗环境、巨噬细胞激活和 T 细胞发育的调节剂。本文报道称,TonEBP 是产热和肥胖的表观遗传调节剂。在小鼠皮下脂肪细胞中,TonEBP 的表达在高脂肪饮食(HFD)喂养后增加了 50 多倍。TonEBP 单倍体缺陷或脂肪细胞特异性 TonEBP 缺陷的小鼠对 HFD 诱导的肥胖和代谢缺陷(高血糖、高血脂和高胰岛素血症)具有抗性。它们还表现出耗氧量增加、对低温的抵抗力增强以及皮下脂肪组织的褐变。TonEBP 在离体和培养的脂肪细胞中抑制β3-肾上腺素能受体基因的启动子,该基因是脂肪分解和产热的关键调节剂。这涉及到 DNMT1 DNA 甲基转移酶的募集和启动子的甲基化。在人类皮下脂肪细胞中,TonEBP 的表达与体重指数呈正相关,但与β3-肾上腺素能受体的表达呈负相关。因此,TonEBP 是肥胖、胰岛素抵抗和高血脂的有吸引力的治疗靶点。