Exendin-4 promotes proliferation of adipose-derived stem cells through PI3K/Akt-Wnt signaling pathways

• Published in: Neuroscience letters Vol. 685; pp. 196 - 202
• Main Authors: Ye, Xiaolu, Cheng, Shimeng, Dong, Yabing, Ren, Jie, Su, Lina, Liu, Jianlan, Zhou, Jing, Liu, Qingmei, Zhu, Ningwen
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 15.10.2018
• Subjects: Adipose-derived stem cell; Exendin-4; GSK3β; PI3K-Akt; Proliferation; Wnt-β-catenin pathway; GSK3β; Proliferation; Adipose-derived stem cell; PI3K-Akt; Wnt-β-catenin pathway; Exendin-4
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2018.06.028

•It’s the first time to evidence that Exendin-4 is effective in promoting ADSCs proliferation via PI3K-Akt-Wnt pathway.•Exendin-4 activates the PI3K-Akt-GSK3β signaling pathway.•Exendin-4 activates the Wnt signaling pathway. Adipose-derived stem cell (ADSC) transplantation has emerged as a potential tool for the treatment of cardiovascular disease and skin wounds. However, with a limited renewal capacity and the need for mass cells during the engraftment, strategies are needed to enhance ADSC proliferative capacity. In this study, we explored the effects of Exendin-4, a glucagon-like peptide-1 analog, on the growth of ADSCs, focusing in particular on phosphatidylinositol 3-kinase (PI3K)-protein kinase B (Akt) and Wnt signaling pathways. Firstly, ADSCs were isolated and cultured in vitro. Then, flow cytometry demonstrated that ADSCs were positive for CD44, CD90 and CD29 but negative for CD31, CD34, and CD45. Exendin-4 (0–200 nM) treatment increased ADSC proliferation. In order to examine specific signaling pathways, a western blotting assay was performed. Our results demonstrate that after treated with 50 nM Exendin-4 for 48 h, the phosphorylation of PI3K, Akt, and GSK3β were increased and phosphorylation of β-catenin was decreased. From these results, we concluded that PI3K-Akt and Wnt-β-catenin signaling pathways mediate Exendin-4 induced ADSC proliferation, the function of which might contribute to the regulation of ADSC proliferation. Our findings provided new insights into the function of the mechanisms underlying Exendin-4 of ADSCs.