Effect of liraglutide on proliferation and differentiation of human adipose stem cells

被引:21
|
作者
Cantini, Giulia [1 ]
Di Franco, Alessandra [1 ]
Samavat, Jinous [1 ]
Forti, Gianni [1 ]
Mannucci, Edoardo [2 ]
Luconi, Michaela [1 ]
机构
[1] Univ Florence, Dept Expt & Clin Biomed Sci, Endocrinol Unit, I-50121 Florence, Italy
[2] Azienda Osped Univ Careggi, Diabet Agcy, I-50141 Florence, Italy
关键词
Glucagone-Like-Peptide-1; Adipogenesis; Adipose stem cells; Weight loss; GLUCAGON-LIKE PEPTIDE-1; OPEN-LABEL; GLP-1; EXENATIDE; RECEPTOR; TWICE; PHARMACOKINETICS; METABOLISM; ANALOG;
D O I
10.1016/j.mce.2014.12.021
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucagon-Like Peptide-1 (GLP-1) receptor agonists, used as glucose-lowering drugs, also induce weight loss by inhibiting food intake. The present study was aimed at the assessment of the in vitro effects of the GLP-1 receptor agonist liraglutide on proliferation and differentiation of human adipose stem cells (ASC) obtained from subcutaneous adipose tissue of morbidly obese subjects undergoing bariatric surgery. Liraglutide (10-100 nM) significantly inhibited ASC proliferation and viability, with a maximum effect at 6 days of culture (45% and 50%, for liraglutide 10 and 100 nM, respectively); the effect was reverted by exendin 9-39. Glucose uptake was significantly reduced by liraglutide in a dose dependent manner. Treatment with liraglutide reduced intracellular lipid accumulation in differentiating ASC, together with FABP-4 mRNA expression (-18%, -23%, -46%, for 1 nM, 10 nM and 100 nM, respectively), whereas it stimulated adiponectin (APN) expression (1.86-, 2.64-, 2.28-fold increase, for 1 nM, 10 nM and 100 nM, respectively). Liraglutide exerts effects on human adipose cell precursors, inhibiting proliferation and differentiation, while stimulating the expression of the insulin-sensitizing adipokine APN. These effects could contribute to the actions of GLP-1 receptor agonists on body weight and insulin sensitivity. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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