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脂肪细胞 Piezo1 通过 FGF1/FGFR1 信号通路在小鼠中介导肥胖性脂肪生成。

Adipocyte Piezo1 mediates obesogenic adipogenesis through the FGF1/FGFR1 signaling pathway in mice.

机构信息

Max Planck Institute for Heart and Lung Research, Department of Pharmacology, Ludwigstr. 43, 61231, Bad Nauheim, Germany.

Cardiovascular Research Center, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Key Laboratory of Environment and Genes Related to Diseases, No.76 West Yanta Road, Yanta District, Xi'an, China.

出版信息

Nat Commun. 2020 May 8;11(1):2303. doi: 10.1038/s41467-020-16026-w.

Abstract

White adipose tissue (WAT) expansion in obesity occurs through enlargement of preexisting adipocytes (hypertrophy) and through formation of new adipocytes (adipogenesis). Adipogenesis results in WAT hyperplasia, smaller adipocytes and a metabolically more favourable form of obesity. How obesogenic WAT hyperplasia is induced remains, however, poorly understood. Here, we show that the mechanosensitive cationic channel Piezo1 mediates diet-induced adipogenesis. Mice lacking Piezo1 in mature adipocytes demonstrated defective differentiation of preadipocyte into mature adipocytes when fed a high fat diet (HFD) resulting in larger adipocytes, increased WAT inflammation and reduced insulin sensitivity. Opening of Piezo1 in mature adipocytes causes the release of the adipogenic fibroblast growth factor 1 (FGF1), which induces adipocyte precursor differentiation through activation of the FGF-receptor-1. These data identify a central feed-back mechanism by which mature adipocytes control adipogenesis during the development of obesity and suggest Piezo1-mediated adipocyte mechano-signalling as a mechanism to modulate obesity and its metabolic consequences.

摘要

肥胖症中白色脂肪组织(WAT)的扩张是通过增大已有脂肪细胞(肥大)和形成新的脂肪细胞(脂肪生成)来实现的。脂肪生成导致 WAT 增生,脂肪细胞变小,肥胖的代谢状态更有利。然而,肥胖相关的 WAT 增生是如何被诱导的,目前仍知之甚少。在这里,我们表明机械敏感阳离子通道 Piezo1 介导了饮食诱导的脂肪生成。当高脂饮食喂养时,成熟脂肪细胞中缺乏 Piezo1 的小鼠表现出前脂肪细胞向成熟脂肪细胞分化的缺陷,导致脂肪细胞增大、WAT 炎症增加和胰岛素敏感性降低。成熟脂肪细胞中 Piezo1 的开放导致脂肪生成因子 1(FGF1)的释放,该因子通过激活 FGF 受体 1 诱导脂肪细胞前体分化。这些数据确定了一个中心反馈机制,通过该机制,成熟脂肪细胞在肥胖的发展过程中控制脂肪生成,并表明 Piezo1 介导的脂肪细胞机械信号传导是调节肥胖及其代谢后果的一种机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24c9/7211025/edb70f95949c/41467_2020_16026_Fig1_HTML.jpg

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