Multiscale analysis of Klf10's impact on the passive mechanical properties of murine skeletal muscle.

Klf10 Mechanical properties Mouse Multiscale Skeletal muscle

Journal

Journal of the mechanical behavior of biomedical materials
ISSN: 1878-0180
Titre abrégé: J Mech Behav Biomed Mater
Pays: Netherlands
ID NLM: 101322406

Informations de publication

Date de publication:
07 Dec 2023
Historique:
received: 13 01 2023
revised: 19 09 2023
accepted: 02 12 2023
medline: 14 12 2023
pubmed: 14 12 2023
entrez: 14 12 2023
Statut: aheadofprint

Résumé

Skeletal muscle is a hierarchical structure composed of multiple organizational scales. A major challenge in the biomechanical evaluation of muscle relates to the difficulty in evaluating the experimental mechanical properties at the different organizational levels of the same tissue. Indeed, the ability to integrate mechanical properties evaluated at various levels will allow for improved assessment of the entire tissue, leading to a better understanding of how changes at each level evolve over time and/or impact tissue function, especially in the case of muscle diseases. Therefore, the purpose of this study was to analyze a genetically engineered mouse model (Klf10 KO: Krüppel-Like Factor 10 knockout) with known skeletal muscle defects to compare the mechanical properties with wild-type (WT) controls at the three main muscle scales: the macroscopic (whole muscle), microscopic (fiber) and submicron (myofibril) levels. Passive mechanical tests (ramp, relaxation) were performed on two types of skeletal muscle (soleus and extensor digitorum longus (EDL)). Results of the present study revealed muscle-type specific behaviors in both genotypes only at the microscopic scale. Interestingly, loss of Klf10 expression resulted in increased passive properties in the soleus but decreased passive properties in the EDL compared to WT controls. At the submicron scale, no changes were observed between WT and Klf10 KO myofibrils for either muscle; these results demonstrate that the passive property differences observed at the microscopic scale (fiber) are not caused by sarcomere intrinsic alterations but instead must originate outside the sarcomeres, likely in the collagen-based extracellular matrix. The macroscopic scale revealed similar passive mechanical properties between WT and Klf10 KO hindlimb muscles. The present study has allowed for a better understanding of the role of Klf10 on the passive mechanical properties of skeletal muscle and has provided reference data to the literature which could be used by the community for muscle multiscale modeling.

Identifiants

pubmed: 38096609
pii: S1751-6161(23)00652-5
doi: 10.1016/j.jmbbm.2023.106298
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106298

Informations de copyright

Crown Copyright © 2023. Published by Elsevier Ltd. All rights reserved.

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

Y Tatarenko (Y)

Sorbonne University, Université de Technologie de Compiègne, CNRS UMR 7338, Biomechanics and Bioengineering, Compiègne, France; ICube, CNRS UMR 7357, University of Strasbourg, Strasbourg, France.

M Li (M)

University of Calgary, Faculty of Kinesiology, Human Performance Laboratory, Calgary, Alberta, Canada.

P Pouletaut (P)

Sorbonne University, Université de Technologie de Compiègne, CNRS UMR 7338, Biomechanics and Bioengineering, Compiègne, France.

M Kammoun (M)

Sorbonne University, Université de Technologie de Compiègne, CNRS UMR 7338, Biomechanics and Bioengineering, Compiègne, France.

J R Hawse (JR)

Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.

V Joumaa (V)

University of Calgary, Faculty of Kinesiology, Human Performance Laboratory, Calgary, Alberta, Canada.

W Herzog (W)

University of Calgary, Faculty of Kinesiology, Human Performance Laboratory, Calgary, Alberta, Canada.

S Chatelin (S)

ICube, CNRS UMR 7357, University of Strasbourg, Strasbourg, France.

S F Bensamoun (SF)

Sorbonne University, Université de Technologie de Compiègne, CNRS UMR 7338, Biomechanics and Bioengineering, Compiègne, France. Electronic address: sabine.bensamoun@utc.fr.

Classifications MeSH