内分泌学
内科学
产热
褐色脂肪组织
白色脂肪组织
FGF21型
产热素
脂肪细胞
脂肪组织
生物
下调和上调
能量稳态
PRDM16
受体
成纤维细胞生长因子
医学
肥胖
基因
生物化学
作者
Osamu Hashimoto,Masayuki Funaba,Kazunari Sekiyama,Satoru Doi,Daichi Shindo,Ryo Satoh,Hiroshi Itoi,Hiroaki Oiwa,Masahiro Morita,Chisato Suzuki,Makoto Sugiyama,Norio Yamakawa,Hitomi Takada,Shigenobu Matsumura,Kazuo Inoue,Seiichi Oyadomari,Hiromu Sugino,Akira Kurisaki
出处
期刊:Cell Reports
[Cell Press]
日期:2018-10-01
卷期号:25 (5): 1193-1203
被引量:59
标识
DOI:10.1016/j.celrep.2018.10.008
摘要
Brown adipocyte activation or beige adipocyte emergence in white adipose tissue (WAT) increases energy expenditure, leading to a reduction in body fat mass and improved glucose metabolism. We found that activin E functions as a hepatokine that enhances thermogenesis in response to cold exposure through beige adipocyte emergence in inguinal WAT (ingWAT). Hepatic activin E overexpression activated thermogenesis through Ucp1 upregulation in ingWAT and other adipose tissues including interscapular brown adipose tissue and mesenteric WAT. Hepatic activin E-transgenic mice exhibited improved insulin sensitivity. Inhibin βE gene silencing inhibited cold-induced Ucp1 induction in ingWAT. Furthermore, in vitro experiments suggested that activin E directly stimulated expression of Ucp1 and Fgf21, which was mediated by transforming growth factor-β or activin type I receptors. We uncovered a function of activin E to stimulate energy expenditure through brown and beige adipocyte activation, suggesting a possible preventive or therapeutic target for obesity.
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