Is cleaved glucagon-like peptide 1 really inactive? Effects of GLP-1(9-36) on human adipose stem cells

被引:7
作者
Cantini, Giulia [1 ]
Di Franco, Alessandra [1 ]
Mannucci, Edoardo [1 ,2 ]
Luconi, Michaela [1 ]
机构
[1] Univ Florence, Dept Expt & Clin Biomed Sci, Endocrinol Unit, Florence, Italy
[2] Careggi Hosp, Diabet Agcy, Florence, Italy
关键词
Adipose stem cells; Glucagon-like peptide-1; Alternative GLP-1R; Dipeptidyl peptidase-4 inhibitors; GLP-1; DIFFERENTIATION; METABOLISM; RECEPTOR; AMIDE;
D O I
10.1016/j.mce.2016.10.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucagon-like peptide 1(9-36) [GLP-1(9-36)] is generated by dipeptidyl peptidase-4 (DPP4) cleavage of the gut incretin hormone, GLP-1(7-36). Since GLP-1(9-36) has a very low affinity for the GLP-1 receptor (GLP-1R), it has so far been considered an inactive form of GLP-1. Here we show GLP-1(9-36) activity in human adipose stem cells (ASC) in vitro. GLR-1(9-36) inhibits human ASC proliferation, glucose uptake and adipogenesis, as well as induces cell apoptosis, to a similar extent as GLP-1(7-36) and liraglutide. Since GLP-1(9-36) effects are not reverted by the receptor antagonist exendin(9-39), which conversely reverts the effects of GLP-1(7-36), we hypothesized that the former may be mediated by a GLP-1 receptor different from the classical pancreatic one. This is the first report of GLP-1(9-36) activity in human adipose cells. Nevertheless, these findings deserve further preclinical studies to better elucidate novel and unforeseen GLP-1(9-36) activities, which could allow a better understanding of the clinical profile of DPP4 inhibitors and GLP-1R agonists. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:10 / 15
页数:6
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