Titel
Molecular Mechanisms of Fetal Tendon Regeneration Versus Adult Fibrous Repair
Autor*in
Iris Ribitsch
VETERM, Equine Surgery Unit, Department of Companion Animals and Horses, University of Veterinary Medicine Vienna
Autor*in
Alexander D. Aldoshin
Chair of Bioinformatics, Department of Biotechnology, Boku University Vienna
... show all
Abstract
Tendinopathies are painful, disabling conditions that afflict 25% of the adult human population. Filling an unmet need for realistic large-animal models, we here present an ovine model of tendon injury for the comparative study of adult scarring repair and fetal regeneration. Complete regeneration of the fetal tendon within 28 days is demonstrated, while adult tendon defects remained macroscopically and histologically evident five months post-injury. In addition to a comprehensive histological assessment, proteome analyses of secretomes were performed. Confirming histological data, a specific and pronounced inflammation accompanied by activation of neutrophils in adult tendon defects was observed, corroborated by the significant up-regulation of pro-inflammatory factors, neutrophil attracting chemokines, the release of potentially tissue-damaging antimicrobial and extracellular matrix-degrading enzymes, and a response to oxidative stress. In contrast, secreted proteins of injured fetal tendons included proteins initiating the resolution of inflammation or promoting functional extracellular matrix production. These results demonstrate the power and relevance of our novel ovine fetal tendon regeneration model, which thus promises to accelerate research in the field. First insights from the model already support our molecular understanding of successful fetal tendon healing processes and may guide improved therapeutic strategies.
Stichwort
tendon healingregenerationinflammationtendinopathyproteomicsanimal modelfetal
Objekt-Typ
Sprache
Englisch [eng]
Persistent identifier
phaidra.univie.ac.at/o:1615013
Erschienen in
Titel
International Journal of Molecular Sciences
Band
22
Ausgabe
11
ISSN
1422-0067
Erscheinungsdatum
2021
Publication
MDPI AG
Fördergeber
Erscheinungsdatum
2021
Zugänglichkeit
Rechteangabe
© 2021 by the authors

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