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TGR5信号传导促进白色脂肪组织的线粒体分裂和米色重塑。

TGR5 signalling promotes mitochondrial fission and beige remodelling of white adipose tissue.

作者信息

Velazquez-Villegas Laura A, Perino Alessia, Lemos Vera, Zietak Marika, Nomura Mitsunori, Pols Thijs Willem Hendrik, Schoonjans Kristina

机构信息

Institute of Bioengineering, Ecole Polytechnique Fédérale de Lausanne, CH-1015, Lausanne, Switzerland.

Abel Salazar Biomedical Sciences Institute, University of Porto, 4050-013, Porto, Portugal.

出版信息

Nat Commun. 2018 Jan 16;9(1):245. doi: 10.1038/s41467-017-02068-0.

Abstract

Remodelling of energy storing white fat into energy expending beige fat could be a promising strategy to reduce adiposity. Here, we show that the bile acid-responsive membrane receptor TGR5 mediates beiging of the subcutaneous white adipose tissue (scWAT) under multiple environmental cues including cold exposure and prolonged high-fat diet feeding. Moreover, administration of TGR5-selective bile acid mimetics to thermoneutral housed mice leads to the appearance of beige adipocyte markers and increases mitochondrial content in the scWAT of Tgr5 mice but not in their Tgr5 littermates. This phenotype is recapitulated in vitro in differentiated adipocytes, in which TGR5 activation increases free fatty acid availability through lipolysis, hence fuelling β-oxidation and thermogenic activity. TGR5 signalling also induces mitochondrial fission through the ERK/DRP1 pathway, further improving mitochondrial respiration. Taken together, these data identify TGR5 as a druggable target to promote beiging with potential applications in the management of metabolic disorders.

摘要

将储存能量的白色脂肪重塑为消耗能量的米色脂肪可能是一种很有前景的减少肥胖的策略。在此,我们表明胆汁酸反应性膜受体TGR5在包括冷暴露和长期高脂饮食喂养在内的多种环境线索下介导皮下白色脂肪组织(scWAT)的米色化。此外,给处于热中性环境的小鼠施用TGR5选择性胆汁酸模拟物会导致米色脂肪细胞标志物的出现,并增加Tgr5小鼠而非其Tgr5同窝小鼠scWAT中的线粒体含量。这种表型在体外分化的脂肪细胞中得到重现,其中TGR5激活通过脂肪分解增加游离脂肪酸的可用性,从而为β氧化和产热活动提供燃料。TGR5信号传导还通过ERK/DRP1途径诱导线粒体分裂,进一步改善线粒体呼吸。综上所述,这些数据确定TGR5是一个可药物靶向的促进米色化的靶点,在代谢紊乱的管理中具有潜在应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8850/5770450/91386ac9ec1b/41467_2017_2068_Fig1_HTML.jpg

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