Microbial regulation of enteroendocrine cells

被引:30
作者
Arora, Tulika [1 ]
Vanslette, Amanda Marie [1 ]
Hjorth, Siv Annegrethe [1 ]
Backhed, Fredrik [1 ,2 ,3 ]
机构
[1] Univ Copenhagen, Novo Nordisk Fdn Ctr Basic Metab Res, Fac Hlth & Med Sci, DK-2200 Copenhagen, Denmark
[2] Univ Gothenburg, Sahlgrenska Acad, Inst Med, Wallenberg Lab,Dept Mol & Clin Med, S-41345 Gothenburg, Sweden
[3] Sahlgrens Univ Hosp, Dept Clin Physiol, Reg Vastra Gotaland, Gothenburg, Sweden
来源
MED | 2021年 / 2卷 / 05期
关键词
GLUCAGON-LIKE PEPTIDE-1; CHAIN FATTY-ACIDS; PROTEIN-COUPLED RECEPTOR; Y GASTRIC BYPASS; VERTICAL SLEEVE GASTRECTOMY; HUMAN GUT MICROBIOME; GLUCOSE-TOLERANCE; BILE-ACIDS; INSULIN-SECRETION; GLP-1; SECRETION;
D O I
10.1016/j.medj.2021.03.018
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
There has been an enormous interest to investigate impact of gut microbiota on host physiology over the past decade. To further understand its role at organismal level, it is important to delineate host-microbiota interaction at tissue and cell level. Diet, antibiotics, disease, or surgery produce shifts in composition of the gut microbiota that further alter levels of microbial-derived metabolites. Enteroendocrine cells (EEGs) are specialized hormone-producing cells in the gut epithelium that sense changes in the intestinal milieu through chemosensing G protein-coupled receptors. Accordingly, microbial metabolites interact with the EECs to stimulate or suppress hormone secretion, which act through endocrine and paracrine signaling to regulate local intestinal and diverse physiological functions and impact overall host metabolism. The remarkable success of glucagon-like peptide-1-based drugs for treatment of type 2 diabetes and obesity highlights the relevance to investigate microbial regulation of EEGs to tackle metabolic diseases through novel microbiota-based therapies.
引用
收藏
页码:553 / 570
页数:18
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