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类 Meteorin 是一种调节免疫-脂肪相互作用以增加米色脂肪产热的激素。

Meteorin-like is a hormone that regulates immune-adipose interactions to increase beige fat thermogenesis.

作者信息

Rao Rajesh R, Long Jonathan Z, White James P, Svensson Katrin J, Lou Jesse, Lokurkar Isha, Jedrychowski Mark P, Ruas Jorge L, Wrann Christiane D, Lo James C, Camera Donny M, Lachey Jenn, Gygi Steven, Seehra Jasbir, Hawley John A, Spiegelman Bruce M

机构信息

Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Cell. 2014 Jun 5;157(6):1279-1291. doi: 10.1016/j.cell.2014.03.065.

Abstract

Exercise training benefits many organ systems and offers protection against metabolic disorders such as obesity and diabetes. Using the recently identified isoform of PGC1-α (PGC1-α4) as a discovery tool, we report the identification of meteorin-like (Metrnl), a circulating factor that is induced in muscle after exercise and in adipose tissue upon cold exposure. Increasing circulating levels of Metrnl stimulates energy expenditure and improves glucose tolerance and the expression of genes associated with beige fat thermogenesis and anti-inflammatory cytokines. Metrnl stimulates an eosinophil-dependent increase in IL-4 expression and promotes alternative activation of adipose tissue macrophages, which are required for the increased expression of the thermogenic and anti-inflammatory gene programs in fat. Importantly, blocking Metrnl actions in vivo significantly attenuates chronic cold-exposure-induced alternative macrophage activation and thermogenic gene responses. Thus, Metrnl links host-adaptive responses to the regulation of energy homeostasis and tissue inflammation and has therapeutic potential for metabolic and inflammatory diseases.

摘要

运动训练对许多器官系统有益,并能预防肥胖和糖尿病等代谢紊乱。我们利用最近鉴定出的PGC1-α异构体(PGC1-α4)作为发现工具,报告了类陨石蛋白(Metrnl)的鉴定,它是一种循环因子,运动后在肌肉中诱导产生,冷暴露时在脂肪组织中诱导产生。增加循环中的Metrnl水平可刺激能量消耗,改善葡萄糖耐量,并增加与米色脂肪产热和抗炎细胞因子相关的基因表达。Metrnl刺激嗜酸性粒细胞依赖性的IL-4表达增加,并促进脂肪组织巨噬细胞的替代性激活,这是脂肪中产热和抗炎基因程序表达增加所必需的。重要的是,在体内阻断Metrnl的作用可显著减弱慢性冷暴露诱导的替代性巨噬细胞激活和产热基因反应。因此,Metrnl将宿主适应性反应与能量稳态和组织炎症的调节联系起来,对代谢和炎症性疾病具有治疗潜力。

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