Evidence map›Paper›PMID 39395701›Full record

ArticleActa biomaterialia2024

Structural determinants of tendon multiscale mechanics and their sensitivity to mechanical stimulation during development in an embryonic chick model.

Benjamin E Peterson, Maria L Canonicco Castro, Helen O McCarthy, Niamh Buckley, Nicholas Dunne, Rebecca A Rolfe, Paula Murphy, Spencer E Szczesny

Abstract read
In one paragraph

Article in Acta biomaterialia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Embryo movement is required for limb tendon maturation.Frontiers in cell and developmental biology · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Benjamin E PetersonDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, USA.
Maria L Canonicco CastroDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, USA.
Helen O McCarthySchool of Pharmacy, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Niamh BuckleySchool of Pharmacy, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Nicholas DunneSchool of Mechanical & Manufacturing Engineering, Dublin City University, Dublin, Ireland.
Rebecca A RolfeDepartment of Zoology, School of Natural Sciences, Trinity College Dublin, Dublin, Ireland.
Paula MurphyDepartment of Zoology, School of Natural Sciences, Trinity College Dublin, Dublin, Ireland.
Spencer E SzczesnyDepartment 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.

Funding

Studying Mechanotransduction in Late Embryonic Development to Inform Tendon Tissue EngineeringR21AR075941 · NIAMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SZCZESNY, SPENCER · 2019 to 2020
$346k
NIAMS NIH HHS R21 AR075941
6 · The paper itself

Abstract

There is an abrupt increase in the multiscale mechanical properties and load-bearing capabilities of tendon during 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 that 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 relationships 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 engineered tendon replacements.

Indexed as

TendonsAnimalsBiomechanical PhenomenaChick EmbryoModels, BiologicalStress, MechanicalCrosslinkingDevelopmentFibrillogenesisMultiscale mechanicsShear lag modelTendon

Identifiers

PMID39395701
PMCPMC11614687

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.