ABSTRACT
Objective
Type 1 diabetes mellitus (T1DM) is an autoimmune disease where immune cells attack insulin-producing beta cells. Islet transplantation is a promising treatment for T1DM. This study aims to evaluate the effects of adipose tissue-derived mesenchymal stem cells (AT-MSCs) in combination with pancreatic islet transplantation using hydrogel.
Methods
T1DM mouse model was established using streptozotocin (STZ). Islets and AT-MSCs were co-embedded in a hydrogel and transplanted into diabetic mice. Five groups with six animals in each (control, hydrogel alone, AT-MSCs embedded hydrogel, islet embedded in hydrogel, and islet + AT-MSCs co-imbedded into a hydrogel) were evaluated in terms of blood glucose, insulin levels and serum and lavage cytokine production.
Results
During 32 days, blood glucose levels decreased from over 400 mg/dl to less than 150 mg/dl in the transplanted mice. Analysis showed increased transformation growth factor beta (TGF-β1) and IL-4 levels, while IL-17 and IFN-γ levels significantly decreased in the MSC-treated groups.
Conclusion
These findings suggest that using AT-MSCs with hydrogel could be a beneficial alternative for enhancing pancreatic islet engraftment and function.
Acknowledgments
We are grateful to colleagues in the Department of Stem Cell Biology, Stem Cell Technology Research Center, for their support during this project. This study was financially supported by grants given by the Iran University of Medical Sciences (IUMS) (Grant No. 23632).
Disclosure Statement
No potential conflict of interest was reported by the author(s).
Data Availability Statement
All data generated during this study are included in this published article.
Authors’ Contributions
B.N.; Performed the experiments. Designed the study and interpreted the data. Wrote the manuscript. J.M.; Performed the experiments, Designed the study and interpreted the data. N.KH.; Review & Editing. M.V; Review & Editing, Visualization. N.T.; Supervision, Project administration, and Funding acquisition. All authors read and approved the final manuscript.