| Literature DB >> 30380411 |
Osamu Hashimoto1, Masayuki Funaba2, Kazunari Sekiyama3, Satoru Doi3, Daichi Shindo3, Ryo Satoh3, Hiroshi Itoi3, Hiroaki Oiwa3, Masahiro Morita3, Chisato Suzuki3, Makoto Sugiyama3, Norio Yamakawa4, Hitomi Takada5, Shigenobu Matsumura6, Kazuo Inoue6, Seiichi Oyadomari7, Hiromu Sugino4, Akira Kurisaki8.
Abstract
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.Entities:
Keywords: Inhbe; activin E; beige adipocyte; brown adipocyte; browning; hepatokine; insulin sensitivity; nonshivering thermogenesis; obesity
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Year: 2018 PMID: 30380411 DOI: 10.1016/j.celrep.2018.10.008
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423