Title of article :
Effects of Exendine-4 on The Differentiation of Insulin Producing Cells from Rat Adipose-Derived Mesenchymal Stem Cells
Author/Authors :
Khorsandi، Layasadat نويسنده Cellular and Molecular Research Center, Jundishapur University of Medical Sciences, Ahvaz, IR Iran , , Saremy، Sadegh نويسنده Cell and Molecular Biology, Center Lab, Jundishapur Medical Science University, Ahvaz, IR Iran , , Khodadadi، Abbas ali نويسنده , , Dehbashi، Fereshteh Negad نويسنده Cellular and Molecular Research Center, Jundishapur University of Medical Sciences, Ahvaz, IR Iran ,
Issue Information :
فصلنامه با شماره پیاپی 68 سال 2016
Pages :
10
From page :
720
To page :
729
Abstract :
Objective: To evaluate the effect of Exendine-4 (EX-4), a Glucagon-like peptide 1 (GLP-1) receptor agonist, on the differentiation of insulin-secreting cells (IPCs) from rat adipose-derived mesenchymal stem cells(ADMSCs). Materials and Methods: In this experimental study, ADMSCs were isolated from rat adipose tissue and exposed to induction media with or without EX-4. After induction, the existence of IPCs was confirmed by morphology analysis, expression pattern analysis of islet-specific genes (Pdx-1, Glut-2 and Insulin) and insulin synthesis and secretion. Results: IPCs induced in presence of EX-4 were morphologically similar to pancreatic islet-like cells. Expression of Pdx-1, Glut-2 and Insulin genes in EX-4 treated cells was significantly higher than the cells exposed to differentiation media without EX-4. Compared to EX-4 untreated ADMSCs, insulin release from EX-4 treated ADMSCs showed a nearly 2.5 fold (P < 0.05) increase when exposed to a high glucose (25 mM) medium. The percentage of insulin positive cells in the EX-4 treated group was approximately 4-fold higher than in the EX-4 untreated ADMSCs. Conclusion: The present study has demonstrated that EX-4 enhances the differentiation of ADMSCs into IPCs. Improvement of this method may help the formation of an unlimited source of cells for transplantation.
Journal title :
Cell Journal (Yakhteh)
Serial Year :
2016
Journal title :
Cell Journal (Yakhteh)
Record number :
2385275
Link To Document :
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