The endocannabinoid system links gut microbiota to adipogenesis

被引:529
作者
Muccioli, Giulio G. [1 ]
Naslain, Damien [2 ]
Backhed, Fredrik [3 ]
Reigstad, Christopher S. [3 ]
Lambert, Didier M.
Delzenne, Nathalie M. [2 ]
Cani, Patrice D. [2 ]
机构
[1] Catholic Univ Louvain, LDRI, Bioanal & Pharmacol Bioact Lipids Lab, B-1200 Brussels, Belgium
[2] Metab & Nutr Res Grp, Brussels, Belgium
[3] Univ Gothenburg, Dept Mol & Clin Med, Sahlgrenska Ctr Cardiovasc & Metab Res, Wallenberg Lab, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
adipose tissue; endocannabinoids; gut microbiota; lipopolysaccharide (LPS); obesity; DIET-INDUCED OBESITY; HIGH-FAT DIET; CANNABINOID TYPE-1 RECEPTOR; HUMAN ABDOMINAL OBESITY; ADIPOSE-TISSUE; INSULIN-RESISTANCE; INDUCED INFLAMMATION; NONALCOHOLIC STEATOHEPATITIS; PREADIPOCYTE DIFFERENTIATION; IMPAIRED ADIPOGENESIS;
D O I
10.1038/msb.2010.46
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
Obesity is characterised by altered gut microbiota, low-grade inflammation and increased endocannabinoid (eCB) system tone; however, a clear connection between gut microbiota and eCB signalling has yet to be confirmed. Here, we report that gut microbiota modulate the intestinal eCB system tone, which in turn regulates gut permeability and plasma lipopolysaccharide (LPS) levels. The impact of the increased plasma LPS levels and eCB system tone found in obesity on adipose tissue metabolism (e. g. differentiation and lipogenesis) remains unknown. By interfering with the eCB system using CB1 agonist and antagonist in lean and obese mouse models, we found that the eCB system controls gut permeability and adipogenesis. We also show that LPS acts as a master switch to control adipose tissue metabolism both in vivo and ex vivo by blocking cannabinoid-driven adipogenesis. These data indicate that gut microbiota determine adipose tissue physiology through LPS-eCB system regulatory loops and may have critical functions in adipose tissue plasticity during obesity. Molecular Systems Biology 6: 392; published online 27 July 2010; doi:10.1038/msb.2010.46 Subject Categories: molecular biology of disease
引用
收藏
页数:15
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