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The promising role of hypoxia-resistant insulin-producing cells in ameliorating diabetes mellitus in vivo.
Ahmed, Hanaa H; Aglan, Hadeer A; Beherei, Hanan H; Mabrouk, Mostafa; Mahmoud, Nadia S.
Afiliação
  • Ahmed HH; Hormones Department, Medical Research & Clinical Studies Institute, National Research Centre, Giza, 12622, Egypt.
  • Aglan HA; Stem Cells Lab, Center of Excellence for Advanced Sciences, National Research Centre, Giza, 12622, Egypt.
  • Beherei HH; Hormones Department, Medical Research & Clinical Studies Institute, National Research Centre, Giza, 12622, Egypt.
  • Mabrouk M; Stem Cells Lab, Center of Excellence for Advanced Sciences, National Research Centre, Giza, 12622, Egypt.
  • Mahmoud NS; Refractories, Ceramics & Building Materials Department, Advanced Materials Technology & Mineral Resources Research Institute, National Research Centre, Giza, 12622, Egypt.
Future Sci OA ; 8(7): FSO811, 2022 Aug.
Article em En | MEDLINE | ID: mdl-36248064
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 CeO2 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Future Sci OA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Future Sci OA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito País de publicação: Reino Unido