GPR120 Is an Omega-3 Fatty Acid Receptor Mediating Potent Anti-inflammatory and Insulin-Sensitizing Effects

被引:2247
作者
Oh, Da Young [1 ]
Talukdar, Saswata [1 ]
Bae, Eun Ju [1 ]
Imamura, Takeshi [2 ]
Morinaga, Hidetaka [1 ]
Fan, WuQiang [1 ]
Li, Pingping [1 ]
Lu, Wendell J. [1 ]
Watkins, Steven M. [3 ]
Olefsky, Jerrold M. [1 ]
机构
[1] Univ Calif San Diego, Dept Med, Div Endocrinol & Metab, La Jolla, CA 92093 USA
[2] Shiga Univ Med Sci, Div Pharmacol, Otsu, Shiga 5202192, Japan
[3] Tethys Biosci, W Sacramento, CA 95691 USA
基金
美国国家卫生研究院;
关键词
FREE FATTY-ACIDS; PROTEIN-COUPLED RECEPTORS; BETA-ARRESTIN; ADIPOSE-TISSUE; OBESITY; INFLAMMATION; RESISTANCE; ACTIVATION; SECRETION; CELLS;
D O I
10.1016/j.cell.2010.07.041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Omega-3 fatty acids (omega-3 FAs), DHA and EPA, exert anti-inflammatory effects, but the mechanisms are poorly understood. Here, we show that the G protein-coupled receptor 120 (GPR120) functions as an omega-3 FA receptor/sensor. Stimulation of GPR120 with omega-3 FAs or a chemical agonist causes broad anti-inflammatory effects in monocytic RAW 264.7 cells and in primary intraperitoneal macrophages. All of these effects are abrogated by GPR120 knock-down. Since chronic macrophage-mediated tissue inflammation is a key mechanism for insulin resistance in obesity, we fed obese WT and GPR120 knockout mice a high-fat diet with or without omega-3 FA supplementation. The omega-3 FA treatment inhibited inflammation and enhanced systemic insulin sensitivity in WT mice, but was without effect in GPR120 knockout mice. In conclusion, GPR120 is a functional omega-3 FA receptor/sensor and mediates potent insulin sensitizing and antidiabetic effects in vivo by repressing macrophage-induced tissue inflammation.
引用
收藏
页码:687 / 698
页数:12
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