GPR41 and GPR43 in Obesity and inflammation - Protective or Causative?

被引:210
作者
Ang, Zhiwei [1 ]
Ding, Jeak Ling [1 ]
机构
[1] Natl Univ Singapore, Fac Sci, Dept Biol Sci, Singapore 117548, Singapore
来源
FRONTIERS IN IMMUNOLOGY | 2016年 / 7卷
基金
英国医学研究理事会;
关键词
GPR41; GPR43; gut microbiota; short-chain fatty acids; obesity and inflammation; FATTY-ACID RECEPTOR; PROTEIN-COUPLED RECEPTOR; GUT MICROBIOTA; HISTONE DEACETYLATION; SODIUM-BUTYRATE; MOUSE MODELS; SUPPRESSION; EXPRESSION; FERMENTATION; ACCUMULATION;
D O I
10.3389/fimmu.2016.00028
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
GPR41 and GPR43 are a pair of mammalian G protein-coupled receptors (GPCRs) expressed in human adipocytes, colon epithelial cells, and peripheral blood mononuclear cells. These receptors are activated by short-chain fatty acids (SCFAs) such as acetate, propionate, and butyrate - which are produced during dietary fiber fermentation by resident gut bacteria. This unique ligand specificity suggests that GPR41 and GPR43 may mediate the interaction between the human host and the gut microbiome. Indeed, studies on knockout mice implicate GPR41 and GPR43 in chronic inflammatory disorders such as obesity, colitis, asthma and arthritis. However, whether GPR41 and GPR43 are protective or causative is inconsistent between studies. This discrepancy may be due to differences in the disease models used, the inbred mouse strains, or non-specific knockout effects. Here, we review the latest findings on GPR41 and GPR43, highlighting contradictory observations. With GPR41 and GPR43 being considered as drug targets, it is pertinent that their role is fully elucidated. We propose that future studies on human tissues, ex vivo, may allow us to confirm the role of GPR41 and GPR43 in humans, be it protective or causative.
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页数:5
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