PRDM16
脂肪生成
脂肪细胞
白色脂肪组织
表观遗传学
褐变
褐色脂肪组织
基因敲除
生物
细胞生物学
产热
H3K4me3
细胞分化
内分泌学
脂肪组织
内科学
基因表达
遗传学
基因
生物化学
发起人
医学
作者
Lin Shuai,Lina Zhang,Bohan Li,Chunlan Tang,Lingyan Wu,Jia Li,Jingya Li
出处
期刊:Diabetes
[American Diabetes Association]
日期:2019-04-22
卷期号:68 (7): 1449-1461
被引量:36
摘要
The unique thermogenic capacity of brown adipocyte makes it an attractive target for antiobesity treatments. Several epigenetic regulators can control brown adipocyte development. In this study, we show that SIRT5, a member of the sirtuins, is required for brown adipocyte differentiation and essential for brown adipogenic gene activation in vitro. Furthermore, we find out that knockdown of SIRT5 reduces intracellular α-ketoglutarate concentration, which leads to elevated H3K9me2 and H3K9me3 levels at promoter regions of Pparγ and Prdm16 loci. Finally, we discover that SIRT5 knockout mice on the Sv129 background exhibit less browning capacity in subcutaneous white adipose tissue compared with controls and show apparent cold intolerance, suggesting that SIRT5 can modulate the browning process in vivo. Thus, our study uncovers a new biological function of SIRT5 in brown adipocyte differentiation and a mechanism by which SIRT5 regulates brown adipogenic gene activation at least partly through an indirect effect on histone modifications. Our study extends the linkage between epigenetics and cell differentiation.
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