Age‐related changes of tendon fibril micro‐morphology and gene expression. Issue 4 (3rd December 2019)

• Record Type: Journal Article
• Authors: Ribitsch, Iris; Gueltekin, Sinan; Keith, Marlies Franziska; Minichmair, Kristina; Peham, Christian; Jenner, Florien; Egerbacher, Monika
• Is Part Of: Journal of anatomy. Volume 236:Issue 4(2020)
• Page Start: 688
• Page End: 700
• Publication Date: 2019-12-03
• Subjects: age -- animal model -- decorin -- equine -- fibril diameter -- gene expression -- horse -- tendon; Anatomy -- Periodicals; 571.3
• DOI: 10.1111/joa.13125
• Languages: English
• ISSNs: 0021-8782

Abstract

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. Abstract : TEM pictures and histograms showing collagen fibril distribution changes for the SDFT and DDFT with age. Whereas a Gaussian‐like distribution of fibril diameters was observed in tendons of foals up to 6 months of age, a marked shift towards much thinner fibrils was seen in tendons of horses 2.75 years of age or older.