Comparison of equine tendon-, muscle-, and bone marrow-derived cells cultured on tendon matrix.
Abstract: To compare viability and biosynthetic capacities of cells isolated from equine tendon, muscle, and bone marrow grown on autogenous tendon matrix. Methods: Cells from 4 young adult horses. Methods: Cells were isolated, expanded, and cultured on autogenous cell-free tendon matrix for 7 days. Samples were analyzed for cell viability, proteoglycan synthesis, collagen synthesis, and mRNA expression of collagen type I, collagen type III, and cartilage oligomeric matrix protein (COMP). Results: Tendon- and muscle-derived cells required less time to reach confluence (approx 2 weeks) than did bone marrow-derived cells (approx 3 to 4 weeks); there were fewer bone marrow-derived cells at confluence than the other 2 cell types. More tendon- and muscle-derived cells were attached to matrices after 7 days than were bone marrow-derived cells. Collagen and proteoglycan synthesis by tendon- and muscle-derived cells was significantly greater than synthesis by bone marrow-derived cells. On a per-cell basis, tendon-derived cells had more collagen synthesis, although this was not significant. Collagen type I mRNA expression was similar among groups. Tendon-derived cells expressed the highest amounts of collagen type III and COMP mRNAs, although the difference for COMP was not significant. Conclusions: Tendon- and muscle-derived cells yielded greater cell culture numbers in shorter time and, on a per-cell basis, had comparable biosynthetic assays to bone marrow-derived cells. More in vitro experiments with higher numbers may determine whether tendon-derived cells are a useful resource for tendon healing.
Publication Date: 2009-06-06 PubMed ID: 19496665DOI: 10.2460/ajvr.70.6.750Google Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research compares the growth and performance of cells from horse tendon, muscle, and bone marrow when cultured on a specific material. Findings indicate that tendon and muscle cells proliferate faster and exhibit higher bioactivity than bone marrow cells.
Methods and Materials
- The study involved cells taken from four young, adult horses.
- These cells were extracted from the selected animals’ tendons, muscles, and bone marrow.
- Once isolated, the cells were then expanded and cultured on a cell-free tendon matrix – a scaffold-like material made from tendons.
- The entire cultivation process lasted for seven days, during which the researchers painstakingly observed the vital attributes of the cells.
Results
- The researchers observed that cells derived from the tendon and muscle reached confluence in approximately two weeks, faster than the bone marrow-derived cells, which took about three to four weeks.
- The number of bone marrow-derived cells observed at confluence was significantly lower compared to the other two types.
- Following seven days of cultivation, more tendon and muscle cells adhered to the tendon matrix than did bone marrow cells.
- Both tendon and muscle cells had greater levels of collagen and proteoglycan synthesis than those derived from bone marrow.
- Among the three cell types, tendon cells showed the highest collagen synthesis on a per-cell basis, but the difference was not statistically significant.
- All three cell types expressed similar levels of collagen type I mRNA, a genetic material related to collagen production.
- Tendon-derived cells had the highest expression of collagen type III and cartilage oligomeric matrix protein (COMP), two components essential for healthy tissues, but the difference in COMP expression among the different cells types was not statistically significant.
Conclusions
- The research showed that compared to bone marrow-derived cells, both tendon and muscle cells yield greater cell culture numbers in a shorter time frame.
- In terms of biosynthetic activity, tendon- and muscle-derived cells were comparable to bone marrow-derived cells.
- Despite these promising results, the authors argued that more experiments with larger sample sizes must be conducted to definitively establish if tendon-derived cells could be used to aid the healing of tendons.
Cite This Article
APA
Stewart AA, Barrett JG, Byron CR, Yates AC, Durgam SS, Evans RB, Stewart MC.
(2009).
Comparison of equine tendon-, muscle-, and bone marrow-derived cells cultured on tendon matrix.
Am J Vet Res, 70(6), 750-757.
https://doi.org/10.2460/ajvr.70.6.750 Publication
Researcher Affiliations
- Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois, Urbana, IL 61802, USA.
MeSH Terms
- Animals
- Bone Marrow Cells / cytology
- Cell Culture Techniques / veterinary
- Culture Media
- Horses / physiology
- Muscle Fibers, Skeletal / cytology
- Tendons / cytology
- Tendons / physiology
Citations
This article has been cited 12 times.- Janczarek I, Kędzierski W, Tkaczyk E, Kaczmarek B, Łuszczyński J, Mucha K. Thermographic Analysis of the Metacarpal and Metatarsal Areas in Jumping Sport Horses and Leisure Horses in Response to Warm-Up Duration.. Animals (Basel) 2021 Jul 6;11(7).
- Shojaee A, Parham A. Strategies of tenogenic differentiation of equine stem cells for tendon repair: current status and challenges.. Stem Cell Res Ther 2019 Jun 18;10(1):181.
- Ceusters J, Lejeune JP, Sandersen C, Niesten A, Lagneaux L, Serteyn D. From skeletal muscle to stem cells: an innovative and minimally-invasive process for multiple species.. Sci Rep 2017 Apr 6;7(1):696.
- Roth SP, Glauche SM, Plenge A, Erbe I, Heller S, Burk J. Automated freeze-thaw cycles for decellularization of tendon tissue - a pilot study.. BMC Biotechnol 2017 Feb 14;17(1):13.
- White NA 2nd, Barrett JG. Magnetic Resonance Imaging-Guided Treatment of Equine Distal Interphalangeal Joint Collateral Ligaments: 2009-2014.. Front Vet Sci 2016;3:73.
- Youngstrom DW, Barrett JG. Engineering Tendon: Scaffolds, Bioreactors, and Models of Regeneration.. Stem Cells Int 2016;2016:3919030.
- Radtke CL, Nino-Fong R, Rodriguez-Lecompte JC, Esparza Gonzalez BP, Stryhn H, McD○ LA. Osteogenic potential of sorted equine mesenchymal stem cell subpopulations.. Can J Vet Res 2015 Apr;79(2):101-8.
- Youngstrom DW, Rajpar I, Kaplan DL, Barrett JG. A bioreactor system for in vitro tendon differentiation and tendon tissue engineering.. J Orthop Res 2015 Jun;33(6):911-8.
- Radtke CL, Nino-Fong R, Esparza Gonzalez BP, McD○ LA. Application of a novel sorting system for equine mesenchymal stem cells (MSCs).. Can J Vet Res 2014 Oct;78(4):290-6.
- Burk J, Erbe I, Berner D, Kacza J, Kasper C, Pfeiffer B, Winter K, Brehm W. Freeze-thaw cycles enhance decellularization of large tendons.. Tissue Eng Part C Methods 2014 Apr;20(4):276-84.
- Via AG, Frizziero A, Oliva F. Biological properties of mesenchymal Stem Cells from different sources.. Muscles Ligaments Tendons J 2012 Jul;2(3):154-62.
- Youngstrom DW, Barrett JG, Jose RR, Kaplan DL. Functional characterization of detergent-decellularized equine tendon extracellular matrix for tissue engineering applications.. PLoS One 2013;8(5):e64151.
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