Free Fatty Acid Receptors 2 and 3 as Microbial Metabolite Sensors to Shape Host Health: Pharmacophysiological View

被引:67
|
作者
Mishra, Sidharth P. [1 ,2 ]
Karunakar, Prashantha [3 ]
Taraphder, Subhash [2 ]
Yadav, Hariom [1 ,4 ]
机构
[1] Wake Forest Sch Med, Dept Internal Med, Mol Med, Winston Salem, NC 27101 USA
[2] West Bengal Univ Anim & Fishery Sci, Dept Anim Genet & Breeding, Kolkata 700037, W Bengal, India
[3] PES Univ, Dept Biotechnol, Bangalore 560085, Karnataka, India
[4] Wake Forest Sch Med, Dept Microbiol & Immunol, Mol Med, Winston Salem, NC 27101 USA
基金
美国国家卫生研究院;
关键词
FFAR2; FFAR3; microbiota; gut; immune; SCFA; PROTEIN-COUPLED RECEPTOR; GUT MICROBIOTA; GENE-EXPRESSION; DIETARY FIBER; ADIPOSE-TISSUE; ENTEROENDOCRINE CELLS; BETA-HYDROXYBUTYRATE; INSULIN-SECRETION; FUNCTIONAL-CHARACTERIZATION; INFLAMMATORY RESPONSES;
D O I
10.3390/biomedicines8060154
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
The role of the gut microbiome in human health is becoming apparent. The major functional impact of the gut microbiome is transmitted through the microbial metabolites that are produced in the gut and interact with host cells either in the local gut environment or are absorbed into circulation to impact distant cells/organs. Short-chain fatty acids (SCFAs) are the major microbial metabolites that are produced in the gut through the fermentation of non-digestible fibers. SCFAs are known to function through various mechanisms, however, their signaling through free fatty acid receptors 2 and 3 (FFAR2/3; type of G-coupled protein receptors) is a new therapeutic approach. FFAR2/3 are widely expressed in diverse cell types in human and mice, and function as sensors of SCFAs to change several physiological and cellular functions. FFAR2/3 modulate neurological signaling, energy metabolism, intestinal cellular homeostasis, immune response, and hormone synthesis. FFAR2/3 function through Gi and/or Gq signaling, that is mediated through specific structural features of SCFAs-FFAR2/3 bindings and modulating specific signaling pathway. In this review, we discuss the wide-spread expression and structural homologies between human and mice FFAR2/3, and their role in different human health conditions. This information can unlock opportunities to weigh the potential of FFAR2/3 as a drug target to prevent human diseases.
引用
收藏
页数:45
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