Structural Determinants of Tendon Multiscale Mechanics and Their Sensitivity to Mechanical Stimulation During Development in an Embryonic Chick Model.

Crosslinking Development Fibrillogenesis Multiscale Mechanics Shear Lag Model Tendon

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
10 Oct 2024
Historique:
received: 01 03 2024
revised: 04 10 2024
accepted: 08 10 2024
medline: 13 10 2024
pubmed: 13 10 2024
entrez: 12 10 2024
Statut: aheadofprint

Résumé

There is an abrupt increase in the multiscale mechanical properties and load-bearing capabilities of tendon during embryonic development. While prior work has identified numerous changes that occur within the collagenous structure during this developmental period, the primary structural elements that give rise to this abrupt increase in mechanical functionality, and their mechanobiological sensitivity, remain unclear. To address this knowledge gap, we used a shear lag model along with ultrastructural imaging, biochemical/thermodynamic assays, and multiscale mechanical testing to investigate the dynamic structure-function relationships during late-stage embryonic chick development and to establish their sensitivity to mechanical stimulation. Mechanical testing and modeling suggested the rapid increase in multiscale mechanics can be explained by increases in fibril length, intrafibrillar crosslinking, and fibril area fraction. To partially test this, we inhibited collagen crosslinking during development and observed a drastic reduction in multiscale mechanical behavior that was explained by a reduction in both fibril modulus and length. Using muscle paralysis to investigate mechanosensitivity, we observed a significantly impaired multiscale mechanical response despite minimal changes in fibril diameter and fibril area fraction. Additionally, the shear lag model found a trend toward lower fibril lengths with paralysis and experimental data found decreased crosslinking and fibril modulus values following flaccid paralysis. Together, these data suggest that both intrafibrillar crosslink formation and fibril elongation are critical to the formation of load-bearing capabilities in tenogenesis and are sensitive to mechanical loading. These findings provide critical insights into the biological and structural mechanisms that give rise to tensile load-bearing soft tissue. STATEMENT OF SIGNIFICANCE: Despite prior work investigating the structural and mechanical changes that occur during tendon development, there has not been a comprehensive analysis of how these simultaneous changes in structure and function are connected. In this study, we performed a comprehensive battery of mechanical and structural assessments of embryonic chick tendons and input these data into a shear lag model to estimate the individual importance of each structural change to the tendon mechanical properties. Additionally, we inhibited muscle activity in the embryos to evaluate the impact of mechanical stimulation on these evolving structure-function during tendon development. These data provide insight into the primary structural elements that produce the tensile load-bearing capabilities of tendon, which will inform efforts to produce tissue engineering tendon replacements.

Identifiants

pubmed: 39395701
pii: S1742-7061(24)00594-4
doi: 10.1016/j.actbio.2024.10.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Benjamin E Peterson (BE)

Department of Biomedical Engineering, Pennsylvania State University, University Park PA, USA.

Maria L Canonicco Castro (ML)

Department of Biomedical Engineering, Pennsylvania State University, University Park PA, USA.

Helen O McCarthy (HO)

School of Pharmacy, Queen's University Belfast, Belfast, Northern Ireland.

Niamh Buckley (N)

School of Pharmacy, Queen's University Belfast, Belfast, Northern Ireland.

Nicholas Dunne (N)

School of Mechanical & Manufacturing Engineering, Dublin City University, Dublin, Ireland.

Rebecca A Rolfe (RA)

Department of Zoology, School of Natural Sciences, Trinity College Dublin, Dublin, Ireland.

Paula Murphy (P)

Department of Zoology, School of Natural Sciences, Trinity College Dublin, Dublin, Ireland.

Spencer E Szczesny (SE)

Department of Biomedical Engineering, Pennsylvania State University, University Park PA, USA; Department of Orthopaedics and Rehabilitation, Pennsylvania State University, Hershey PA, USA. Electronic address: ses297@psu.edu.

Classifications MeSH