Cited by 375Muscle Physiology and DisordersSpaceflight effects on biologyCardiac Fibrosis and Remodeling

Macrophages promote muscle membrane repair and muscle fibre growth and regeneration during modified muscle loading in mice in vivo

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Tidball, James G., Wehling‐Henricks, Michelle·2007·The Journal of Physiology

Abstract

Muscle injury or modified muscle use can stimulate muscle invasion by leucocytes that have the potential to increase tissue damage or promote tissue growth and repair. In the present investigation, we examined the role of macrophages in muscle injury, repair and regeneration during modified muscle loading. Weight-bearing was removed from the hindlimbs of mice for 10 days followed by reloading through normal ambulation. During the unloading period, soleus muscle fibre cross-section decreased by 38%. Prior to the onset of reloading, mice received a series of intraperitoneal injections of anti-F4/80, which binds a mouse macrophage surface antigen. Although anti-F4/80 injections did not affect macrophage numbers in soleus muscles at 2 days of reloading, macrophages were reduced by 86% at 4 days of reloading. Muscle membrane lysis during the reloading period did not differ at 2 days of reloading between anti-F4/80-treated mice and mice that received isotype control antibody. However, control animals showed large decreases in the number of fibres with membrane lesions at 4 days of reloading, but this membrane repair did not occur in macrophage-depleted mice. Macrophage-depletion also reduced muscle regeneration (indicated by central nucleation) and satellite cell differentiation (indicated by reductions in MyoD-expressing satellite cells) and prevented growth of muscle fibres that normally occurred in control animals between days 2 and 4 of reloading. These findings collectively sh…

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Crossref · 10.1113/jphysiol.2006.118265

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  • Depletion of circulating monocytes reduces removal of cellular debris and delays muscle tissue remodeling after injury.

    “A number of studies have shown that reduction of the number of monocytes available to participate in the response following muscle injury via depletion of circulating cells results in slowed removal of cellular debris and delayed muscle tissue remodeling [112–114].”
  • The M2 environment attenuates inflammation and cytotoxic nitric oxide and drives differentiation and fusion of cells.

    “The transition to an M2 environment not only serves to attenuate the inflammatory response and potentially cytotoxic production of nitric oxide, but also to drive the differentiation and fusion of cells [114,124].”

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References 45 · Cited by 375

Authors
Tidball, J. G., & Wehling‐Henricks, M.
Affiliations
University of California, Los Angeles (US)
Venue
The Journal of Physiology
Publisher
Wiley
Published
2006-12-21
Volume
578
Issue
1
Pages
327-336
ISSN
  • 0022-3751 (ISSN-L)
  • 1469-7793
OpenAlex
W2098940221
Cited by
375
References
45
Citations by year
2026: 8 · 2025: 11 · 2024: 14 · 2023: 10 · 2022: 10 · 2021: 27 · 2020: 22 · 2019: 25 · 2018: 18 · 2017: 16 · 2016: 17 · 2015: 21 · 2014: 27 · 2013: 32 · 2012: 25
FWCI
5.84
Type
journal article
Language
en
Open access
Locations
  • The Journal of Physiology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR047855, AR-47721, R01AR047721, AR47855)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Health Sciences › Medicine › Physiology › Spaceflight effects on biology
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
Keywords
macrophages, muscle regeneration, muscle membrane repair, muscle unloading, muscle reloading, muscle atrophy, satellite cells, MyoD, soleus muscle, muscle damage
MeSH terms
Animals, Cell Differentiation, Cell Membrane, Cell Membrane Permeability, Immunohistochemistry, Macrophages, Mice, Inbred C57BL, Regeneration, MyoD Protein, Muscle, Skeletal, Muscle Fibers, Skeletal, Satellite Cells, Skeletal Muscle, Mice

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