Nature communications · 2019
TonEBP/NFAT5 promotes obesity and insulin resistance by epigenetic suppression of white adipose tissue beiging.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Lee Hwan Hee, An Seung Min, Ye Byeong Jin, Lee Jun Ho, Yoo Eun Jin, Jeong Gyu Won, Kang Hyun Je, Alfadda Assim A, Lim Sun Woo, Park Jiyoung, Lee-Kwon Whaseon, Kim Jae Bum, Choi Soo Youn, Kwon Hyug Moo
Аннотация
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.
Предметные рубрики MeSH
3T3 CellsAdipocytesAdipose Tissue, BeigeAnimalsBody Mass IndexDNA (Cytosine-5-)-Methyltransferase 1DNA MethylationDiet, High-FatDisease Models, AnimalEnergy MetabolismEpigenesis, GeneticHEK293 CellsHumansInsulin ResistanceMaleMiceMice, TransgenicMicroRNAsObesityPrimary Cell CultureReceptors, Adrenergic, beta-3Subcutaneous FatThermogenesisTranscription Factors