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Updated: May 23, 2026

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Isolation and Identification of Mesenchymal Stem Cells Derived from Adipose Tissue of Sprague Dawley Rats
Published on: April 7, 2023
Interaction between adipose tissue-derived mesenchymal stem cells and regulatory T-cells
Anja U Engela1, Carla C Baan, Annemiek M A Peeters
1Department of Internal Medicine, Transplantation Laboratory/Nephrology, Erasmus University Medical Center, Rotterdam, The Netherlands. a.grohnert@erasmusmc.nl
Cell Transplantation
|April 5, 2012
Summary
Allogeneic mesenchymal stem cells (MSCs) and host regulatory T-cells (Tregs) do not impede each other
Area of Science:
- Immunology
- Cell Therapy
- Transplantation Science
Background:
- Mesenchymal stem cells (MSCs) possess immunosuppressive properties, making them promising for cell therapy in transplant recipients.
- The functional interaction between allogeneic MSCs and host regulatory T-cells (Tregs) remains unclear.
Purpose of the Study:
- To investigate the reciprocal functional influence between adipose tissue-derived MSCs (ASCs) from kidney donors and host Tregs.
- To assess the impact of Tregs on ASC immunomodulatory capacity and vice versa in the context of kidney transplantation.
Main Methods:
- Utilized perirenal adipose tissue-derived MSCs (ASCs) from kidney donors.
- Co-cultured ASCs with regulatory T-cells (Tregs) from healthy donors and kidney recipients 6 months post-transplantation.
- Assessed immune cell function, cytokine secretion (IFN-γ, TNF-α, IL-10), and indoleamine 2,3-dioxygenase (IDO) expression.
Main Results:
- ASCs' immunomodulatory capacity was unaffected by Tregs from both healthy donors and transplant recipients.
- Tregs supported ASC function without altering IFN-γ secretion, indicating ASC activation and efficiency.
- ASCs suppressed immune responses via IDO expression, reduced TNF-α, and induced IL-10 production in effector cells and Tregs.
Conclusions:
- Donor ASCs and recipient Tregs do not negatively impact each other's function.
- This mutual functional compatibility supports the potential of MSC therapy for preventing graft rejection in solid organ transplantation.
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