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Review
. 2025 Apr 19;15(8):1175.
doi: 10.3390/ani15081175.

Mesenchymal Stem Cells in Veterinary Medicine-Still Untapped Potential

Affiliations
Review

Mesenchymal Stem Cells in Veterinary Medicine-Still Untapped Potential

Magdalena Morawska-Kozłowska et al. Animals (Basel). .

Abstract

Mesenchymal stem cells (MSCs) hold significant therapeutic potential in veterinary medicine due to their regenerative and immunomodulatory properties. This review examines the clinical applications of MSCs across multiple animal species, including equine, canine, feline, and bovine medicine. MSC therapies have demonstrated promising outcomes in treating musculoskeletal disorders, osteoarthritis, inflammatory diseases, and tissue injuries, particularly in horses and dogs. In cats, MSCs show potential for managing chronic kidney disease, inflammatory bowel disease, and asthma, while in bovine medicine, they offer alternative treatment approaches for mastitis and orthopedic injuries. Despite these advancements, challenges such as treatment standardization, cell sourcing, and potential adverse effects, including tumorigenicity, remain under investigation. The emerging field of MSC-based veterinary medicine highlights its capacity to enhance healing, reduce inflammation, and improve clinical outcomes. However, further research is necessary to optimize treatment protocols and address safety concerns, ensuring the widespread adoption of MSC therapies in veterinary practice.

Keywords: MSC; stem cell therapy; stem cells; veterinary regenerative medicine.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
(A). Microscopic image of stem cell differentiation into a chondrocyte population. The picture shows a chondrocyte monolayer. Own research. (B). Mesenchymal stem cells are obtained from a bitch uterus. Own research.
Figure 2
Figure 2
A diagram showing mesenchymal stem cells’ influence on the body’s immune response. Red arrows represent negative impacts, and green arrows represent positive impacts. Abbreviations: PGE2: prostaglandin E2; IFN-γ: interferon-γ; TNF-α: tumor necrosis factor-α; TGF-β1: transforming growth factor-β1; IDO: indoleamine-pyrrole 2,3-dioxygenase; IL: interleukin; PD-1/PD-L1: programmed death-1/programmed death-ligand 1; CCR6: chemokine receptor 6; CCL-2: C-C motif chemokine ligand 2; CCL-18: C-C motif chemokine ligand 18.

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