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The promising role of hypoxia-resistant insulin-producing cells in ameliorating diabetes mellitus in vivo

AIM: This study aimed to evaluate the efficacy of hypoxia-persistent insulin-producing cells (IPCs) against diabetes in vivo. MATERIALS & METHODS: Mesenchymal stem cells (MSCs) differentiation into IPCs in the presence of Se/Ti (III) or CeO(2) nanomaterials. IPCs were subjected to hypoxia and hy...

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Detalles Bibliográficos
Autores principales: Ahmed, Hanaa H, Aglan, Hadeer A, Beherei, Hanan H, Mabrouk, Mostafa, Mahmoud, Nadia S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540411/
https://www.ncbi.nlm.nih.gov/pubmed/36248064
http://dx.doi.org/10.2144/fsoa-2022-0005
Descripción
Sumario:AIM: This study aimed to evaluate the efficacy of hypoxia-persistent insulin-producing cells (IPCs) against diabetes in vivo. MATERIALS & METHODS: Mesenchymal stem cells (MSCs) differentiation into IPCs in the presence of Se/Ti (III) or CeO(2) nanomaterials. IPCs were subjected to hypoxia and hypoxia genes were analyzed. PKH-26-labeled IPCs were infused in diabetic rats to evaluate their anti-diabetic potential. RESULTS: MSCs were differentiated into functional IPCs. IPCs exhibited overexpression of anti-apoptotic genes and down-expression of hypoxia and apoptotic genes. IPCs implantation elicited glucose depletion and elevated insulin, HK and G6PD levels. They provoked VEGF and PDX-1 upregulation and HIF-1α and Caspase-3 down-regulation. IPCs transplantation ameliorated the destabilization of pancreatic tissue architecture. CONCLUSION: The chosen nanomaterials were impressive in generating hypoxia-resistant IPCs that could be an inspirational strategy for curing diabetes.