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Updated: Jan 29, 2026

Isolation of Rat Adipose Tissue Mesenchymal Stem Cells for Differentiation into Insulin-producing Cells
Published on: August 29, 2022
In vitro differentiation of human multilineage differentiating stress-enduring (Muse) cells into insulin producing
Ali M Fouad1, Mahmoud M Gabr1, Elsayed K Abdelhady2
1Department of Biotechnology, Urology and Nephrology Center, Mansoura 35516, Egypt.
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 ± 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.
Insights
Muse cells, a rare subpopulation within mesenchymal stem cells (MSCs), demonstrate superior potential for generating insulin-producing cells (IPCs). This study highlights Muse cells as a promising source for functional IPCs.
Area of Science:
- Stem cell biology
- Cellular differentiation
- Endocrinology
Background:
- Mesenchymal stem cells (MSCs) are a heterogeneous cell population.
- Muse cells represent a rare, pluripotent subpopulation within MSCs.
- Understanding Muse cell characteristics is crucial for regenerative medicine.
Purpose of the Study:
- To evaluate the pluripotency of Muse cells.
- To compare the ability of Muse cells versus non-Muse cells in generating insulin-producing cells (IPCs) after in vitro differentiation.
- To assess the functionality of generated IPCs.
Main Methods:
- Isolation of Muse cells from adipose-derived MSCs using FACSAria III cell sorter.
- Evaluation of pluripotency markers and stage-specific embryonic antigen-3 (SSEA-3) expression.
- In vitro differentiation protocol followed by flow cytometry and confocal microscopy to assess IPC generation and insulin production.
Main Results:
- Muse cells constituted approximately 3.2% of MSCs, with 82% expressing SSEA-3.
- Pluripotent markers were significantly higher in Muse cells compared to non-Muse cells.
- A higher percentage of functional IPCs, expressing insulin and C-peptide, were generated from Muse cells.
Conclusions:
- Muse cells are identified as a distinct adult pluripotent subpopulation.
- Muse cells possess a superior capacity for generating functional insulin-producing cells compared to non-Muse cells.
- These findings suggest Muse cells hold significant potential for cell-based therapies in diabetes treatment.
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