脂肪组织
化学
受体
脂联素
内分泌学
内科学
3T3-L1
细胞培养
基因表达
细胞生物学
生物化学
脂肪细胞
生物
胰岛素抵抗
胰岛素
基因
医学
遗传学
作者
Hiroshi Nagasaki,Takaaki Kondo,Masahiro Fuchigami,Hiroyuki Hashimoto,Yoshihisa Sugimura,Nobuaki Ozaki,Hiroshi Arima,Akira Ota,Yutaka Oiso,Yoji Hamada
出处
期刊:FEBS Letters
[Wiley]
日期:2012-01-10
卷期号:586 (4): 368-372
被引量:84
标识
DOI:10.1016/j.febslet.2012.01.001
摘要
In this study we aimed to identify the physiological roles of G protein‐coupled receptor 84 (GPR84) in adipose tissue, together with medium‐chain fatty acids (MCFAs), the specific ligands for GPR84. In mice, high‐fat diet up‐regulated GPR84 expression in fat pads. In 3T3‐L1 adipocytes, co‐culture with a macrophage cell line, RAW264, or TNFα remarkably enhanced GPR84 expression. In the presence of TNFα, MCFAs down‐regulated adiponectin mRNA expression in 3T3‐L1 adipocytes. Taken together, our results suggest that GPR84 emerges in adipocytes in response to TNFα from infiltrating macrophages and exacerbates the vicious cycle between adiposity and diabesity.
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