| Literature DB >> 32041793 |
Mari Lilith Lund1, Giovanni Sorrentino2, Kristoffer Lihme Egerod1, Chantal Kroone3, Brynjulf Mortensen4, Filip Krag Knop1,4,5,6, Frank Reimann7, Fiona M Gribble7, Daniel J Drucker8, Eelco J P de Koning9,10, Kristina Schoonjans2, Fredrik Bäckhed1,11, Thue W Schwartz1,12, Natalia Petersen13.
Abstract
Glucagon-like peptide 1 (GLP-1) mimetics are effective drugs for treatment of type 2 diabetes, and there is consequently extensive interest in increasing endogenous GLP-1 secretion and L-cell abundance. Here we identify G-protein-coupled bile acid receptor 1 (GPBAR1) as a selective regulator of intestinal L-cell differentiation. Lithocholic acid and the synthetic GPBAR1 agonist, L3740, selectively increased L-cell density in mouse and human intestinal organoids and elevated GLP-1 secretory capacity. L3740 induced expression of Gcg and transcription factors Ngn3 and NeuroD1 L3740 also increased the L-cell number and GLP-1 levels and improved glucose tolerance in vivo. Further mechanistic examination revealed that the effect of L3740 on L cells required intact GLP-1 receptor and serotonin 5-hydroxytryptamine receptor 4 (5-HT4) signaling. Importantly, serotonin signaling through 5-HT4 mimicked the effects of L3740, acting downstream of GLP-1. Thus, GPBAR1 agonists and other powerful GLP-1 secretagogues facilitate L-cell differentiation through a paracrine GLP-1-dependent and serotonin-mediated mechanism.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32041793 PMCID: PMC7224989 DOI: 10.2337/db19-0764
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461