TonEBP/NFAT5 promotes obesity and insulin resistance by epigenetic suppression of white adipose tissue beiging.
Hwan Hee LeeSeung Min AnByeong Jin YeJun Ho LeeEun Jin YooGyu Won JeongHyun Je KangAssim A AlfaddaSun Woo LimJiyoung ParkWhaseon Lee-KwonJae Bum KimSoo Youn ChoiHyug Moo KwonPublished in: Nature communications (2019)
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.
Keyphrases
- adipose tissue
- insulin resistance
- high fat diet
- high fat diet induced
- dna methylation
- binding protein
- transcription factor
- polycystic ovary syndrome
- poor prognosis
- gene expression
- body mass index
- endothelial cells
- genome wide
- type diabetes
- physical activity
- skeletal muscle
- long non coding rna
- high glucose
- signaling pathway
- immune response
- smoking cessation
- drug induced
- induced pluripotent stem cells