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Published on: August 1, 2020
Mesenchymal Stem Cell Therapy on Tendon/Ligament Healing.
Connie S Chamberlain1, Erin E Saether1, Erdem Aktas2
1Department of Orthopedics and Rehabilitation, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Mesenchymal stem/stromal cells (MSCs) can improve ligament and tendon healing by reprogramming inflammatory cells. Pre-conditioned MSCs significantly enhanced tissue repair and strength, outperforming unconditioned MSCs in animal models.
Area of Science:
- Regenerative Medicine
- Immunology
- Biomaterials Science
Background:
- Ligament and tendon rupture healing typically results in scar tissue, compromising function.
- Early suppression of inflammation is key to achieving more regenerative healing.
- Mesenchymal stem/stromal cells (MSCs) can modulate the immune response during healing by reprogramming macrophages.
Purpose of the Study:
- To investigate the efficacy of MSCs in treating ligament and tendon injuries by modulating the inflammatory response.
- To evaluate the dose-dependent effects of MSCs on ligament healing.
- To assess the impact of pre-conditioned MSCs on inflammation and tissue repair.
Main Methods:
- Allogeneic mesenchymal stem/stromal cells (MSCs) were administered to rat medial collateral ligament (MCL) and Achilles tendon injury models.
- Dose-dependency studies compared low (1 × 10^6) and high (4 × 10^6) doses of MSCs.
- Pre-conditioned MSCs, designed for enhanced anti-inflammatory properties, were compared to unconditioned MSCs.
Main Results:
- A low dose of MSCs reduced inflammation and M1 macrophages in MCL healing, improving ligament strength.
- Pre-conditioned MSCs significantly decreased inflammation by shifting macrophages from M1 to M2 phenotypes.
- Treatment with pre-conditioned MSCs restored tissue strength to levels comparable to intact tissue.
Conclusions:
- MSC therapy holds promise for improving ligament and tendon healing.
- Pre-conditioning MSCs enhances their anti-inflammatory and regenerative capabilities.
- MSC treatment, particularly with pre-conditioned cells, promotes a more robust, paracrine-mediated immunosuppressive response for superior tissue repair.
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