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TonEBP/NFAT5 promotes obesity and insulin resistance by epigenetic suppression of white adipose tissue beiging

机译:TINEBP / NFAT5通过表观抑制的白色脂肪抑制促进肥胖和胰岛素抵抗力

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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.
机译:滋生响应增强剂结合蛋白(Typebp或NFAT5)是对高渗,巨噬细胞活化和T细胞发育的细胞适应的调节因子。在这里,我们举报Tinebp是热生成和肥胖的表观遗传调节因子。在小鼠皮下adipocytes中,TypeBP表达响应高脂饮食(HFD)喂养而增加?> 50倍。具有Tonybp Haplo缺乏或脂肪细胞特异性TineBP缺乏的小鼠对HFD诱导的肥胖和代谢缺陷(高血糖,高脂血症和高胰岛素血症)抵抗力。它们还显示出增加的氧气消耗,耐低温和皮下脂肪组织的抗病。 TINEBP在离体和培养的脂肪细胞中抑制β3-肾上腺素受体基因的启动子,脂肪分解和热生成的临界调节剂。这涉及募集DNMT1 DNA甲基酶和启动子的甲基化。在人皮下脂肪细胞中,TINEBP表达显示与体重指数的相关性,但与β3-肾上腺素表达的反比相关。因此,TINEBP是一种有吸引力的肥胖,胰岛素抵抗和高脂血症的治疗靶标。

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