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Journal of anatomy2019; 236(4); 688-700; doi: 10.1111/joa.13125

Age-related changes of tendon fibril micro-morphology and gene expression.

Abstract: Aging is hypothesized to be associated with changes in tendon matrix composition which may lead to alteration of tendon material properties and hence propensity to injury. Altered gene expression may offer insights into disease pathophysiology and thus open new perspectives toward designing pathophysiology-driven therapeutics. Therefore, the current study aimed at identifying naturally occurring differences in tendon micro-morphology and gene expression of newborn, young and old horses. Age-related differences in the distribution pattern of tendon fibril thickness and in the expression of the tendon relevant genes collagen type 1 (Col1), Col3, Col5, tenascin-C, decorin, tenomodulin, versican, scleraxis and cartilage oligomeric matrix protein were investigated. A qualitative and quantitative gene expression and collagen fibril diameter analysis was performed for the most frequently injured equine tendon, the superficial digital flexor tendon, in comparison with the deep digital flexor tendon. Most analyzed genes (Col1, Col3, Col5, tenascin-C, tenomodulin, scleraxis) were expressed at a higher level in foals (age ≤ 6 months) than in horses of 2.75 years (age at which flexor tendons become mature in structure) and older, decorin expression increased with age. Decorin was previously reported to inhibit the lateral fusion of collagen fibrils, causing a thinner fibril diameter with increased decorin concentration. The results of this study suggested that reduction of tendon fibril diameters commonly seen in equine tendons with increasing age might be a natural age-related phenomenon leading to greater fibril surface areas with increased fibrillar interaction and reduced sliding at the fascicular/fibrillar interface and hence a stiffer interfascicular/interfibrillar matrix. This may be a potential reason for the higher propensity to tendinopathies with increasing age.
Publication Date: 2019-12-03 PubMed ID: 31792963PubMed Central: PMC7083562DOI: 10.1111/joa.13125Google Scholar: Lookup
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  • Journal Article

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.

The study investigates how aging influences the micro-structure and gene expression in tendons, using horses as the subject. The findings could potentially help understand why tendons are more prone to injury as they age.

Objectives and Methodology

  • The research aimed to identify changes in tendon micro-structure and gene expression in newborn, young, and old horses. This could assist in understanding the changes in the tendon matrix with aging and how this influences tendon properties and susceptibility to injury.
  • Researchers examined age-related differences in tendon fibril thickness and tendon-related gene expressions – specifically collagen type 1 (Col1), Col3, Col5, tenascin-C, decorin, tenomodulin, versican, scleraxis and cartilage oligomeric matrix protein.
  • The study mainly focused on the superficial digital flexor tendon, which is the tendon most frequently injured in horses, compared with the deep digital flexor tendon.

Results and Implications

  • Most of the analyzed genes (including Col1, Col3, Col5, tenascin-C, tenomodulin, scleraxis) were expressed at a higher level in foals (age ≤ 6 months) than in horses aged 2.75 years and older.
  • The study found decorin gene expression increased with age, which is significant as decorin is known to inhibit the lateral fusion of collagen fibrils, resulting in a slimmer fibril diameter with increased decorin concentration.
  • The research suggests that the reduction of tendon fibril diameters often seen in horse tendons as they age could be a natural phenomenon. This might create greater fibril surface areas, increased fibrillar interaction and reduced sliding at the fascicular/fibrillar interface, thus a stiffer interfascicular/interfibrillar matrix.
  • This hardening and stiffening of the tendon matrix with age may explain why there is a higher propensity for tendinopathies in older horses. This increased susceptibility to tendon problems with age is possibly due to the micro-structural and gene expression changes identified in this study.
  • The results could open up new possibilities for the design of therapies aimed at the inherent pathophysiology of tendon diseases, thus benefiting both animals and potentially humans as well.

Cite This Article

APA
Ribitsch I, Gueltekin S, Keith MF, Minichmair K, Peham C, Jenner F, Egerbacher M. (2019). Age-related changes of tendon fibril micro-morphology and gene expression. J Anat, 236(4), 688-700. https://doi.org/10.1111/joa.13125

Publication

ISSN: 1469-7580
NlmUniqueID: 0137162
Country: England
Language: English
Volume: 236
Issue: 4
Pages: 688-700

Researcher Affiliations

Ribitsch, Iris
  • Department for Companion Animals and Horses, Veterm, University Equine Hospital, Vetmeduni Vienna, Vienna, Austria.
Gueltekin, Sinan
  • Department for Companion Animals and Horses, Veterm, University Equine Hospital, Vetmeduni Vienna, Vienna, Austria.
Keith, Marlies Franziska
  • Department of Pathobiology, Unit of Histology and Embryology, Vetmeduni Vienna, Vienna, Austria.
Minichmair, Kristina
  • Department of Pathobiology, Unit of Histology and Embryology, Vetmeduni Vienna, Vienna, Austria.
Peham, Christian
  • Department for Companion Animals and Horses, Veterm, University Equine Hospital, Vetmeduni Vienna, Vienna, Austria.
Jenner, Florien
  • Department for Companion Animals and Horses, Veterm, University Equine Hospital, Vetmeduni Vienna, Vienna, Austria.
Egerbacher, Monika
  • Department of Pathobiology, Unit of Histology and Embryology, Vetmeduni Vienna, Vienna, Austria.

MeSH Terms

  • Age Factors
  • Aging / physiology
  • Animals
  • Collagen / genetics
  • Collagen / metabolism
  • Decorin / genetics
  • Decorin / metabolism
  • Gene Expression
  • Horses
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Tendons / metabolism

Conflict of Interest Statement

The authors declare that they have no conflict of interests.

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