Literature DB >> 35050792

Diaphragm muscle fibrosis involves changes in collagen organization with mechanical implications in Duchenne muscular dystrophy.

Ridhi Sahani1, C Hunter Wallace1, Brian K Jones1, Silvia S Blemker1,2,3.   

Abstract

In Duchenne muscular dystrophy (DMD), diaphragm muscle dysfunction results in respiratory insufficiency, a leading cause of death in patients. Increased muscle stiffness occurs with buildup of fibrotic tissue, characterized by excessive accumulation of extracellular matrix (ECM) components such as collagen, and prevents the diaphragm from achieving the excursion lengths required for respiration. However, changes in mechanical properties are not explained by collagen amount alone and we must consider the complex structure and mechanics of fibrotic tissue. The goals of our study were to 1) determine if and how collagen organization changes with the progression of DMD in diaphragm muscle tissue and 2) predict how collagen organization influences the mechanical properties of the ECM. We first visualized collagen structure with scanning electron microscopy (SEM) images and then developed an analysis framework to quantify collagen organization and generate image-based finite-element models. Image analysis revealed increased collagen fiber straightness and alignment in mdx over wild type (WT) at 3 mo (straightness: mdx = 0.976 ± 0.0108, WT = 0.887 ± 0.0309, alignment: mdx = 0.876 ± 0.0333, WT = 0.759 ± 0.0416) and 6 mo (straightness: mdx = 0.942 ± 0.0182, WT = 0.881 ± 0.0163, alignment: mdx = 0.840 ± 0.0315, WT = 0.759 ± 0.0368). Collagen fibers retained a transverse orientation relative to muscle fibers (70°-90°) in all groups. Mechanical models predicted an increase in the transverse relative to longitudinal (muscle fiber direction) stiffness, with stiffness ratio (transverse/longitudinal) increased in mdx over WT at 3 mo (mdx = 5.45 ± 2.04, WT = 1.97 ± 0.670) and 6 mo (mdx = 4.05 ± 0.985, WT = 1.96 ± 0.506). This study revealed changes in diaphragm ECM structure and mechanics during disease progression in the mdx muscular dystrophy mouse phenotype, highlighting the need to consider the role of collagen organization on diaphragm muscle function.NEW & NOTEWORTHY Scanning electron microscopy images of decellularized diaphragm muscle from WT and mdx, Duchenne muscular dystrophy model, mice revealed that collagen fibers in the epimysium are oriented transverse to muscle fibers, with age- and disease-dependent changes in collagen arrangement. Finite-element models generated from these images predicted that changes in collagen arrangement during disease progression influence the mechanical properties of the extracellular matrix. Thus, changes in collagen fiber-level structure are implicated on tissue-level properties during fibrosis.

Entities:  

Keywords:  Duchenne muscular dystrophy; collagen organization; extracellular matrix mechanics; fibrosis

Mesh:

Substances:

Year:  2022        PMID: 35050792      PMCID: PMC9076426          DOI: 10.1152/japplphysiol.00248.2021

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  76 in total

1.  Ligament material behavior is nonlinear, viscoelastic and rate-independent under shear loading.

Authors:  Jeffrey A Weiss; John C Gardiner; Carlos Bonifasi-Lista
Journal:  J Biomech       Date:  2002-07       Impact factor: 2.712

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Journal:  J Physiol       Date:  2016-12-14       Impact factor: 5.182

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Journal:  Muscle Nerve       Date:  2011-02       Impact factor: 3.217

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9.  Spatial and age-related changes in the microstructure of dystrophic and healthy diaphragms.

Authors:  Catherine C Henry; Kyle S Martin; Bridget B Ward; Geoffrey G Handsfield; Shayn M Peirce; Silvia S Blemker
Journal:  PLoS One       Date:  2017-09-06       Impact factor: 3.240

10.  An improved method for studying mouse diaphragm function.

Authors:  Chady H Hakim; Thais B Lessa; Gregory J Jenkins; Nora N Yang; Carlos E Ambrosio; Dongsheng Duan
Journal:  Sci Rep       Date:  2019-12-19       Impact factor: 4.379

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  1 in total

1.  Characterisation of Progressive Skeletal Muscle Fibrosis in the Mdx Mouse Model of Duchenne Muscular Dystrophy: An In Vivo and In Vitro Study.

Authors:  Matteo Giovarelli; Francesca Arnaboldi; Silvia Zecchini; Laura Brigida Cornaghi; Ambra Nava; Michele Sommariva; Emilio Giuseppe Ignazio Clementi; Nicoletta Gagliano
Journal:  Int J Mol Sci       Date:  2022-08-05       Impact factor: 6.208

  1 in total

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