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Equine veterinary journal2012; 45(2); 193-198; doi: 10.1111/j.2042-3306.2012.00600.x

Autologous point-of-care cellular therapies variably induce equine mesenchymal stem cell migration, proliferation and cytokine expression.

Abstract: Autologous cellular therapy products including adipose-derived stromal vascular fraction (SVF), bone marrow mononuclear cells (BMMNs), cord blood mononuclear cells (CBMNs) and platelet rich plasma are options for treatment of acute orthopaedic lesions while mesenchymal stem cells (MSCs) are culture expanded. These products may contribute to healing by secreting matrix proteins or growth factors, but they may also act on endogenous MSCs to facilitate healing. Objective: To determine the effects of cell therapy products on MSCs function in vitro. The hypothesis was that cell therapy products promote MSCs functions including proliferation, migration and mediator release. Methods: Fat, bone marrow (BM), cord blood and platelets were obtained from 6 Quarter Horses. The BM-MSCs and their autologous cell therapy products were co-incubated in transwells. Mesenchymal stem cells proliferation, migration, gene expression and cytokine concentrations were determined. Results: All cell therapy products increased MSCs proliferation, but SVF induced significantly more proliferation than any other product. Also SVF elicited more MSCs chemotaxis and, along with BMMNs, significantly more MSCs chemoinvasion. Cord blood mononuclear cells stimulated MSCs to produce high concentrations of interleukin-6 (IL-6), transforming growth factor-β1 (TGF-β1), and prostaglandin E(2) (PGE(2)). Stromal vascular fraction and platelet lysate did not stimulate MSCs but SVF and platelet lysate themselves contained high concentrations of PGE(2) and IL-6 (SVF) and TGF-β1 (platelet lysate). Conclusions: Autologous cell products variably stimulate MSCs functions with 2 primary patterns apparent. Products either contained preformed mediators that may have intrinsic healing function, or products stimulated MSCs to secrete mediators. Conclusions: The specific clinical indications for these products may differ to include administration as a sole treatment modality prior to MSCs injection for intrinsic cell and cytokine activity (i.e. SVF) or administration concurrently with MSCs to activate MSCs for treatment of chronic lesions (i.e. CBMNs).
Publication Date: 2012-07-11 PubMed ID: 22780195DOI: 10.1111/j.2042-3306.2012.00600.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article investigates how autologous cell therapy products affect the function of equine mesenchymal stem cells (MSCs). It was found that these products can enhance MSC proliferation, migration, and mediator release, with varying degrees of stimulation observed. The clinical implications of these results suggest different uses for these products, either alone or in combination with MSCs for diverse lesion treatments.

Methodology

  • The study used adipose-derived stromal vascular fraction (SVF), bone marrow mononuclear cells (BMMNs), cord blood mononuclear cells (CBMNs) and platelet-rich plasma, which are all types of autologous cell therapy products.
  • These products were obtained from 6 Quarter Horses, specifically from their fat, bone marrow, cord blood, and platelets.
  • The researchers co-incubated these cell therapy products with bone marrow-derived MSCs in transwells to observe their effects.
  • The proliferation, migration, gene expression, and cytokine concentrations of the MSCs were then determined.

Results

  • The research found that all cell therapy products increased the proliferation of MSCs.
  • Among all products, SVF induced the highest level of proliferation and chemotaxis in MSCs, also eliciting significant chemoinvasion alongside BMMNs.
  • Stimulation with cord blood mononuclear cells resulted in the MSCs producing high concentrations of interleukin-6 (IL-6), transforming growth factor-β1 (TGF-β1), and prostaglandin E (PGE). However, SVF and platelet lysate did not stimulate MSCs, but they themselves contained high concentrations of PGE, IL-6 (SVF), and TGF-β1 (platelet lysate).
  • The results highlighted two primary patterns of how these cell therapy products stimulate MSCs. They either contained ready mediators with a potential healing function, or they stimulated the MSCs to secrete these healing mediators.

Conclusions

  • The findings suggest that the specific clinical uses for these cell therapy products might differ. Some might be used as a standalone treatment option for their inherent cell and cytokine activity (like SVF) or given alongside MSCs to trigger their action for the treatment of chronic lesions (like CBMNs).
  • In brief, the study demonstrated varying effects of autologous cell therapy products on the function of equine MSCs, indicating their potential role in the treatment of acute orthopedic lesions.

Cite This Article

APA
Kol A, Walker NJ, Galuppo LD, Clark KC, Buerchler S, Bernanke A, Borjesson DL. (2012). Autologous point-of-care cellular therapies variably induce equine mesenchymal stem cell migration, proliferation and cytokine expression. Equine Vet J, 45(2), 193-198. https://doi.org/10.1111/j.2042-3306.2012.00600.x

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 45
Issue: 2
Pages: 193-198

Researcher Affiliations

Kol, A
  • Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, USA.
Walker, N J
    Galuppo, L D
      Clark, K C
        Buerchler, S
          Bernanke, A
            Borjesson, D L

              MeSH Terms

              • Adipose Tissue / cytology
              • Adipose Tissue / physiology
              • Animals
              • Blood Platelets
              • Bone Marrow Transplantation / methods
              • Cell Culture Techniques / methods
              • Cell Proliferation
              • Chemotaxis
              • Cytokines / genetics
              • Cytokines / metabolism
              • Fetal Blood / cytology
              • Gene Expression Regulation / physiology
              • Mesenchymal Stem Cells / cytology
              • Mesenchymal Stem Cells / physiology
              • Point-of-Care Systems

              Citations

              This article has been cited 8 times.
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              3. Bogers SH. Cell-Based Therapies for Joint Disease in Veterinary Medicine: What We Have Learned and What We Need to Know. Front Vet Sci 2018;5:70.
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                pubmed: 27733784
              5. Tyrnenopoulou P, Karayannopoulou M, Angelopoulou S, Pyrros A, Mparous E, Koliakos G, Diakakis N. Successful management of an equine carpal chip fracture by intra-articularly injected adipose-derived stromal vascular fraction after arthroscopic removal. Iran J Vet Res 2016 Winter;17(1):59-61.
                pubmed: 27656232
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                doi: 10.1177/1947603513487553pubmed: 26069674google scholar: lookup
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              8. Gabrielyan A, Knaak S, Gelinsky M, Arnhold S, Rösen-Wolff A. Hypoxia-conditioned media allows species-specific attraction of bone marrow stromal cells without need for recombinant proteins. BMC Vet Res 2014 Mar 4;10:56.
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