Comparative study of the properties of tendinocytes derived from three different sites in the equine superficial digital flexor tendon.
Abstract: This aim of this study was to determine the characteristic differences in tendinocytes derived from three sites of the equine superficial digital flexor tendon (SDFT)-proximally the myotendinous junction (MTJ), mid-metacarpal (mM) and osteotendinous junction (OTJ)-in morphology, proliferation, and ability for synthesis of collagen and matrix metalloproteinases (MMPs). Little difference was observed in cell proliferation. Addition of tumor necrosis factor (TNF) alpha to the culture medium resulted in increased collagen synthesis by tendinocytes from all three sites. The amount of collagen synthesized by tendinocytes derived from the mM and OTJ was much larger than that synthesized by untreated tendinocytes. A collagen zymogram revealed that proMMP-13 synthesis was increased towards the distal site. However, TNFalpha treatment resulted in a significant decrease in the amount of proMMP-13 synthesized by tendinocytes from all three sites. On the other hand, a gelatin zymogram showed that the synthesis level of proMMP-9 tended to decrease towards the distal site, but there was little difference between synthesis levels of proMMP-9 before and after TNFalpha treatment. These results indicated that tendinocytes in the same tendon have different characteristics and that these characterisities would reflect the function of tendinocytes in vivo. Also, the isolated tendinocytes provided much information on the characteristics and properties of tendons for the ECM turnover system and on the responsiveness of tendinocytes to complex inflammatory responses in a tendinopathy condition.
Publication Date: 2010-03-06 PubMed ID: 20203418DOI: 10.2220/biomedres.31.35Google Scholar: Lookup
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- Comparative Study
- Journal Article
Summary
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The research compares the cell properties of tendinocytes (cells that form tendons) from different parts of a horse’s superficial digital flexor tendon. The study found that these cells displayed different characteristics such as morphology, proliferation, and collagen and matrix metalloproteinases (MMPs) synthesis abilities, which could reflect their function in the living organism.
Cellular Differences Within the Same Tendon
- The research sought to understand the differences in tendinocytes that were derived from three different locations within the superficial digital flexor tendon (SDFT) – the myotendinous junction (MTJ), mid-metacarpal (mM), and osteotendinous junction (OTJ).
- The researchers examined differences in cell morphology (structure), proliferation (growth and multiplication), and their ability to synthesize collagen and matrix metalloproteinases (MMPs). Collagen is a protein responsible for providing structural support in connective tissues, whereas MMPs have a role in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling.
Influence of Tumor Necrosis Factor (TNF) Alpha
- The study found that the addition of tumor necrosis factor (TNF) alpha to the culture medium led to an increase in collagen synthesis in tendinocytes from all three sites.
- Interestingly, the amount of collagen made by tendinocytes from the mM and OTJ sites was much larger than by those without TNF alpha treatment.
Impact on Matrix Metalloproteinase (MMP) Synthesis
- In terms of MMP synthesis, the study revealed that the production of proMMP-13, an inactive form of the enzyme, increased towards the distal site (further from the body’s centre).
- However, upon the administration of TNF alpha, the amount of proMMP-13 produced by tendinocytes from all three sites significantly decreased.
- Contrarily, the synthesis level of proMMP-9 (another MMP enzyme) didn’t show much difference before and after the treatment with TNF alpha, but its production trend decreased towards the distal site.
Functional Implications and Future Potential
- These findings led to the conclusion that locations within the same tendon have tendinocytes with different characteristics, which may reflect their specific functions in vivo (within the living body).
- Isolated tendinocytes could provide insights into the properties and functionality of tendons, especially concerning the extracellular matrix turnover system (the process of tissue repair and remodelling).
- Furthermore, the research highlighted how tendinocytes respond to complex inflammatory responses, which could be useful for understanding conditions like tendinopathy where tendon inflammation occurs.
Cite This Article
APA
Hosaka YZ, Uratsuji T, Ueda H, Uehara M, Takehana K.
(2010).
Comparative study of the properties of tendinocytes derived from three different sites in the equine superficial digital flexor tendon.
Biomed Res, 31(1), 35-44.
https://doi.org/10.2220/biomedres.31.35 Publication
Researcher Affiliations
- Department of Veterinary Anatomy, Tottori University, Japan. y-hosa@muses.tottori-u.ac.jp
MeSH Terms
- Animals
- Cell Proliferation
- Cells, Cultured
- Collagen / biosynthesis
- Enzyme Precursors / biosynthesis
- Gene Expression Regulation / drug effects
- Gene Expression Regulation / physiology
- Horses
- Matrix Metalloproteinase 13 / biosynthesis
- Matrix Metalloproteinase 9 / biosynthesis
- Tendons / cytology
- Tendons / metabolism
- Tumor Necrosis Factor-alpha / pharmacology
Citations
This article has been cited 5 times.- Chisari E, Rehak L, Khan WS, Maffulli N. Tendon healing is adversely affected by low-grade inflammation.. J Orthop Surg Res 2021 Dec 4;16(1):700.
- Oh SY, Kim DK, Han SH, Lee HH, Jeong Y, Baek M, Kim H, Ahn W, Lee S. Sustained Exposure of Substance P Causes Tendinopathy.. Int J Mol Sci 2020 Nov 16;21(22).
- Morita W, Dakin SG, Snelling SJB, Carr AJ. Cytokines in tendon disease: A Systematic Review.. Bone Joint Res 2017 Dec;6(12):656-664.
- Biasutti S, Dart A, Smith M, Blaker C, Clarke E, Jeffcott L, Little C. Spatiotemporal variations in gene expression, histology and biomechanics in an ovine model of tendinopathy.. PLoS One 2017;12(10):e0185282.
- Nemoto M, Kizaki K, Yamamoto Y, Oonuma T, Hashizume K. Tenascin-C Expression in Equine Tendon-derived Cells During Proliferation and Migration.. J Equine Sci 2013;24(2):17-24.
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