Analyze Diet
Equine veterinary journal2013; 46(5); 589-595; doi: 10.1111/evj.12142

In vitro analysis of equine, bone marrow-derived mesenchymal stem cells demonstrates differences within age- and gender-matched horses.

Abstract: Stem cell therapies are used routinely in equine practice. Most published reports characterise stem cells derived from younger horses; however, middle-aged horses are often in athletic performance, and experience degenerative medical conditions. Thus, mesenchymal stem cells (MSCs) from this group should be investigated. Objective: To describe differences in in vitro adherence, proliferation and potential for differentiation of equine bone marrow-derived MSCs (equine BMMSCs) harvested from middle-aged (10-13 years old) female donors. Methods: Descriptive study of stem cell characteristics. Methods: Equine BMMSCs from 6 horses were cultured in vitro and evaluated for viability, proliferation, osteogenesis, chondrogenesis, adipogenesis, cluster-of-differentiation markers and gene expression. Results: Equine BMMSCs from all 6 donors demonstrated fibroblastic, cellular morphology, adherence to plastic and expression of cluster-of-differentiation markers. They varied in their rate of proliferation and trilineage differentiation. The equine BMMSCs of one of 6 donors demonstrated a higher rate of proliferation, enhanced ability for cell passaging and a more robust in vitro differentiation. Comparatively, equine BMMSCs from 2 donors demonstrated a lower rate of proliferation and lack of osteogenic and chondrogenic differentiation. Conclusions: The results of this study confirm that donor-to-donor variation in equine BMMSCs exists and this variation can be documented using in vitro assays. Subjective assessment suggests that the rate of proliferation tends to correlate with differentiation potential.
Publication Date: 2013-12-17 PubMed ID: 23855680DOI: 10.1111/evj.12142Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This study examined the differences in the characteristics and behaviour of stem cells derived from middle-aged horses’ bone marrow. It found notable variations among donors in aspects such as cell proliferation and the potential for differentiation into specific types of cells.

Research Background and Objective

  • The study was prompted by the common use of stem cell therapies in equine practice, typically using cells from younger horses. However, middle-aged horses often continue to have athletic use and develop degenerative medical conditions, warranting investigation into the potential of their stem cells.
  • The main objective was to observe any differences among stem cells from middle-aged (10-13 years old) female horses, in terms of their ability to stick to surfaces (adherence), multiply (proliferation), and change into different cell types (differentiation).

Methods

  • The researchers conducted an in-depth study of the stem cells’ features, cultivating them in a laboratory setting (in vitro).
  • Bone marrow-derived mesenchymal stem cells (BMMSCs) were collected from 6 horses and examined for several criteria, including cell survival, multiplication, potential for differentiation into bone, cartilage and fat cells, presence of specific surface markers, and gene expression.

Results

  • All the harvested stem cells showed the expected properties of fibroblastic cell shape, the ability to stick to plastic, and characteristically expressed markers.
  • Notably, there were appreciable differences in the rate of cell multiplication and the capacity for differentiation into three cell types. One of the six horse donors’ stem cells showed a high rate of multiplication, better potential for maintaining a cell line, and robust ability to differentiate in the laboratory setting.
  • In contrast, stem cells from two other donors showed a lower multiplication rate and failed to differentiate into bone and cartidge cells.

Conclusions

  • The findings confirmed the existence of donor-to-donor variation in horse BMMSCs, as highlighted by the in vitro assays used in the study.
  • The researchers also observed a tendency for higher rates of cell multiplication to go hand-in-hand with better potential for differentiation. This implies that more robust cell proliferation might signal a greater therapeutic potential of stem cells from certain donors.

Cite This Article

APA
Carter-Arnold JL, Neilsen NL, Amelse LL, Odoi A, Dhar MS. (2013). In vitro analysis of equine, bone marrow-derived mesenchymal stem cells demonstrates differences within age- and gender-matched horses. Equine Vet J, 46(5), 589-595. https://doi.org/10.1111/evj.12142

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 46
Issue: 5
Pages: 589-595

Researcher Affiliations

Carter-Arnold, J L
  • Department of Large Animal Clinical Sciences, University of Tennessee, USA.
Neilsen, N L
    Amelse, L L
      Odoi, A
        Dhar, M S

          MeSH Terms

          • Animals
          • Biomarkers
          • Bone Marrow Cells / cytology
          • Bone Marrow Cells / physiology
          • Cell Differentiation
          • Cell Proliferation
          • Cell Survival
          • Cells, Cultured
          • Female
          • Gene Expression Regulation / physiology
          • Horses / physiology
          • Mesenchymal Stem Cells / cytology
          • Mesenchymal Stem Cells / physiology

          Citations

          This article has been cited 16 times.
          1. Caruso M, Shuttle S, Amelse L, Elkhenany H, Schumacher J, Dhar MS. A pilot study to demonstrate the paracrine effect of equine, adult allogenic mesenchymal stem cells in vitro, with a potential for healing of experimentally-created, equine thoracic wounds in vivo.. Front Vet Sci 2022;9:1011905.
            doi: 10.3389/fvets.2022.1011905pubmed: 36452146google scholar: lookup
          2. Bowers K, Amelse L, Bow A, Newby S, MacDonald A, Sun X, Anderson D, Dhar M. Mesenchymal Stem Cell Use in Acute Tendon Injury: In Vitro Tenogenic Potential vs. In Vivo Dose Response.. Bioengineering (Basel) 2022 Aug 22;9(8).
            doi: 10.3390/bioengineering9080407pubmed: 36004932google scholar: lookup
          3. Nino-Fong R, Esparza Gonzalez BP, Rodriguez-Lecompte JC, Montelpare W, McD○ L. Development of a biologically immortalized equine stem cell line.. Can J Vet Res 2021 Oct;85(4):293-301.
            pubmed: 34602734
          4. Zayed M, Adair S, Dhar M. Effects of Normal Synovial Fluid and Interferon Gamma on Chondrogenic Capability and Immunomodulatory Potential Respectively on Equine Mesenchymal Stem Cells.. Int J Mol Sci 2021 Jun 15;22(12).
            doi: 10.3390/ijms22126391pubmed: 34203758google scholar: lookup
          5. Lee HJ, Lee H, Na CB, Song IS, Ryu JJ, Park JB. Evaluation of the Age- and Sex-Related Changes of the Osteogenic Differentiation Potentials of Healthy Bone Marrow-Derived Mesenchymal Stem Cells.. Medicina (Kaunas) 2021 May 22;57(6).
            doi: 10.3390/medicina57060520pubmed: 34067350google scholar: lookup
          6. Ribitsch I, Oreff GL, Jenner F. Regenerative Medicine for Equine Musculoskeletal Diseases.. Animals (Basel) 2021 Jan 19;11(1).
            doi: 10.3390/ani11010234pubmed: 33477808google scholar: lookup
          7. Bagge J, MacLeod JN, Berg LC. Cellular Proliferation of Equine Bone Marrow- and Adipose Tissue-Derived Mesenchymal Stem Cells Decline With Increasing Donor Age.. Front Vet Sci 2020;7:602403.
            doi: 10.3389/fvets.2020.602403pubmed: 33363241google scholar: lookup
          8. MacDonald ES, Barrett JG. The Potential of Mesenchymal Stem Cells to Treat Systemic Inflammation in Horses.. Front Vet Sci 2019;6:507.
            doi: 10.3389/fvets.2019.00507pubmed: 32039250google scholar: lookup
          9. Colbath AC, Dow SW, Hopkins LS, Phillips JN, McIlwraith CW, Goodrich LR. Single and repeated intra-articular injections in the tarsocrural joint with allogeneic and autologous equine bone marrow-derived mesenchymal stem cells are safe, but did not reduce acute inflammation in an experimental interleukin-1β model of synovitis.. Equine Vet J 2020 Jul;52(4):601-612.
            doi: 10.1111/evj.13222pubmed: 31821594google scholar: lookup
          10. Pessôa LVF, Pires PRL, Del Collado M, Pieri NCG, Recchia K, Souza AF, Perecin F, da Silveira JC, de Andrade AFC, Ambrosio CE, Bressan FF, Meirelles FV. Generation and miRNA Characterization of Equine Induced Pluripotent Stem Cells Derived from Fetal and Adult Multipotent Tissues.. Stem Cells Int 2019;2019:1393791.
            doi: 10.1155/2019/1393791pubmed: 31191664google scholar: lookup
          11. Roberts EL, Dang T, Lepage SIM, Alizadeh AH, Walsh T, Koch TG, Kallos MS. Improved expansion of equine cord blood derived mesenchymal stromal cells by using microcarriers in stirred suspension bioreactors.. J Biol Eng 2019;13:25.
            doi: 10.1186/s13036-019-0153-8pubmed: 30949237google scholar: lookup
          12. Baird A, Lindsay T, Everett A, Iyemere V, Paterson YZ, McClellan A, Henson FMD, Guest DJ. Osteoblast differentiation of equine induced pluripotent stem cells.. Biol Open 2018 May 10;7(5).
            doi: 10.1242/bio.033514pubmed: 29685993google scholar: lookup
          13. Zayed M, Caniglia C, Misk N, Dhar MS. Donor-Matched Comparison of Chondrogenic Potential of Equine Bone Marrow- and Synovial Fluid-Derived Mesenchymal Stem Cells: Implications for Cartilage Tissue Regeneration.. Front Vet Sci 2016;3:121.
            doi: 10.3389/fvets.2016.00121pubmed: 28149840google scholar: lookup
          14. Pezzanite LM, Fortier LA, Antczak DF, Cassano JM, Brosnahan MM, Miller D, Schnabel LV. Equine allogeneic bone marrow-derived mesenchymal stromal cells elicit antibody responses in vivo.. Stem Cell Res Ther 2015 Apr 12;6(1):54.
            doi: 10.1186/s13287-015-0053-xpubmed: 25889095google scholar: lookup
          15. Visser J, Levett PA, te Moller NC, Besems J, Boere KW, van Rijen MH, de Grauw JC, Dhert WJ, van Weeren PR, Malda J. Crosslinkable hydrogels derived from cartilage, meniscus, and tendon tissue.. Tissue Eng Part A 2015 Apr;21(7-8):1195-206.
            doi: 10.1089/ten.TEA.2014.0362pubmed: 25557049google scholar: lookup
          16. Cruz Villagrán C, Amelse L, Neilsen N, Dunlap J, Dhar M. Differentiation of equine mesenchymal stromal cells into cells of neural lineage: potential for clinical applications.. Stem Cells Int 2014;2014:891518.
            doi: 10.1155/2014/891518pubmed: 25506367google scholar: lookup