Short Term High Fat Diet Challenge Promotes Alternative Macrophage Polarization in Adipose Tissue via Natural Killer T Cells and Interleukin-4

被引:123
作者
Ji, Yewei [1 ]
Sun, Shengyi [2 ]
Xia, Sheng [1 ]
Yang, Liu
Li, Xiaoqing [1 ]
Qi, Ling [1 ,2 ]
机构
[1] Cornell Univ, Div Nutr Sci, Ithaca, NY 14853 USA
[2] Cornell Univ, Grad Program Biochem Mol & Cell Biol, Ithaca, NY 14853 USA
基金
美国国家卫生研究院;
关键词
INDUCED INSULIN-RESISTANCE; INVARIANT NKT CELLS; IN-VIVO; LIVER-DISEASE; ACTIVATION; INFLAMMATION; OBESITY; MECHANISM; SENSITIVITY; PRECURSOR;
D O I
10.1074/jbc.M112.371807
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inflammation in adipose tissue plays an important role in the pathogenesis of obesity-associated complications. However, the detailed cellular events underlying the inflammatory changes at the onset of obesity have not been characterized. Here we show that an acute HFD challenge is unexpectedly associated with elevated alternative (M2) macrophage polarization in adipose tissue mediated by Natural Killer T (NKT) cells. Upon 4d HFD feeding, NKT cells are activated, promote M2 macrophage polarization and induce arginase 1 expression via interleukin (IL)-4 in adipose tissue, not in the liver. In NKT-deficient CD1d(-/-) mice, M2 macrophage polarization in adipose tissue is reduced while systemic glucose homeostasis and insulin tolerance are impaired upon 4d HFD challenge. Thus, our study demonstrate, for the first time to our knowledge, that acute HFD feeding is associated with remarkably pronounced and dynamic immune responses in adipose tissue, and adipose-resident NKT cells may link acute HFD feeding with inflammation.
引用
收藏
页码:24378 / 24386
页数:9
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