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In vitro differentiation of human multilineage differentiating stress-enduring (Muse) cells into insulin producing cells.
Fouad, Ali M; Gabr, Mahmoud M; Abdelhady, Elsayed K; Zakaria, Mahmoud M; Khater, Sherry M; Ismail, Amani M; Refaie, Ayman F.
Afiliação
  • Fouad AM; Department of Biotechnology, Urology and Nephrology Center, Mansoura 35516, Egypt.
  • Gabr MM; Department of Biotechnology, Urology and Nephrology Center, Mansoura 35516, Egypt.
  • Abdelhady EK; Department of Zoology, Faculty of Science, Mansoura University, Mansoura 35516, Egypt.
  • Zakaria MM; Department of Biotechnology, Urology and Nephrology Center, Mansoura 35516, Egypt.
  • Khater SM; Department of Biotechnology, Urology and Nephrology Center, Mansoura 35516, Egypt.
  • Ismail AM; Department of Biotechnology, Urology and Nephrology Center, Mansoura 35516, Egypt.
  • Refaie AF; Nephrology Department, Urology and Nephrology Center, Mansoura 35516, Egypt.
J Genet Eng Biotechnol ; 16(2): 433-440, 2018 Dec.
Article em En | MEDLINE | ID: mdl-30733757
ABSTRACT
Mesenchymal stem cells (MSCs) is a heterogeneous population. Muse cells is a rare pluripotent subpopulation within MSCs. This study aims to evaluate the pulirpotency and the ability of Muse cells to generate insulin producing cells (IPCs) after in vitro differentiation protocol compared to the non-Muse cells. Muse cells were isolated by FACSAria III cell sorter from adipose-derived MSCs and were evaluated for its pluripotency. Following in vitro differentiation, IPCs derived from Muse and non-Muse cells were evaluated for insulin production. Muse cells comprised 3.2 ±â€¯0.7% of MSCs, approximately 82% of Muse cells were positive for anti stage-specific embryonic antigen-3 (SSEA-3). Pluripotent markers were highly expressed in Muse versus non-Muse cells. The percentage of generated IPCs by flow cytometric analysis was higher in Muse cells. Under confocal microscopy, Muse cells expressed insulin and c-peptide while it was undetected in non-Muse cells. Our results introduced Muse cells as a new adult pluripotent subpopulation, which is capable to produce higher number of functional IPCs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Genet Eng Biotechnol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Genet Eng Biotechnol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Egito