Cited by 99Muscle Physiology and DisordersWound Healing and TreatmentsCardiac Fibrosis and Remodeling

Regeneration versus fibrosis in skeletal muscle

Moyer, Adam L., Wagner, Kathryn R.·2011·Current Opinion in Rheumatology

Abstract

PURPOSE OF REVIEW: This review evaluates recently published literature examining various muscle tissue cells and their modulators that determine whether injured skeletal muscle will fully regenerate or become fibrotic. RECENT FINDINGS: Muscle regeneration is a complex process involving several interacting cell types. Macrophages initiate a cytokine response to injury that both directs the subsequent inflammatory response and promotes nonmyeloid proliferation. Muscle cells and their progenitors produce autocrine and paracrine growth factors that help inhibit or stimulate muscle growth and regeneration. Cells of the connective tissue, including fibroblasts and newly described fibro/adipogenic progenitors, can support myogenic cells and remodel the extracellular matrix. However in certain environments, fibrosis can become a self-perpetuating process leading to incomplete muscle regeneration. SUMMARY: Several cell types are involved in the muscle repair process, interacting through multiple signaling molecules and pathways. This provides a richness of potential therapeutic targets to reduce fibrosis and facilitate skeletal muscle regeneration.

Integrity signals

Registry

Crossref · 10.1097/bor.0b013e32834bac92

Cites

29 of 29 references verified0 citation errors · 0 not checkable

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  • Chronic inflammation and persistent Mp accumulation are often associated with tissue destruction and fibrosis.

    “However, chronic inflammation and persistent Mp accumulation are often associated with tissue destruction and fibrosis [6 -8].”

    From Macrophage phenotypes during tissue repair (2013) · cites this paper as [7]

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Authors
Moyer, A. L., & Wagner, K. R.
Affiliations
Kennedy Krieger Institute (US)
Corresponding author
Wagner, Kathryn R.
Venue
Current Opinion in Rheumatology
Published
2011-11
Volume
23
Issue
6
Pages
568-573
ISSN
1040-8711 (ISSN-L)
OpenAlex
W2314732254
Cited by
99
References
29
Citations by year
2026: 4 · 2025: 5 · 2024: 7 · 2023: 4 · 2022: 4 · 2021: 8 · 2020: 12 · 2019: 2 · 2018: 8 · 2017: 5 · 2016: 8 · 2015: 7 · 2014: 4 · 2013: 14 · 2012: 7
FWCI
3.24
Type
journal article
Language
en
Open access
closed
Locations
  • Current Opinion in Rheumatology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Muscular Dystrophy Association
  • National Institutes of Health
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
Keywords
skeletal muscle regeneration, muscle fibrosis, muscle damage, macrophages, inflammation, cytokines, myogenic progenitor cells, fibroblasts, fibro-adipogenic progenitors, extracellular matrix remodeling, growth factors, muscle repair
MeSH terms
Animals, Connective Tissue Cells, Fibrosis, Humans, Regeneration, Signal Transduction, Muscle, Skeletal, Muscle Fibers, Skeletal, Myoblasts, Skeletal

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