The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Highly Efficient, Functional Engraftment of Skeletal Muscle Stem Cells in Dystrophic Muscles
Open accessAbstract
Satellite cells reside beneath the basal lamina of skeletal muscle fibers and include cells that act as precursors for muscle growth and repair. Although they share a common anatomical localization and typically are considered a homogeneous population, satellite cells actually exhibit substantial heterogeneity. We used cell-surface marker expression to purify from the satellite cell pool a distinct population of skeletal muscle precursors (SMPs) that function as muscle stem cells. When engrafted into muscle of dystrophin-deficient mdx mice, purified SMPs contributed to up to 94% of myofibers, restoring dystrophin expression and significantly improving muscle histology and contractile function. Transplanted SMPs also entered the satellite cell compartment, renewing the endogenous stem cell pool and participating in subsequent rounds of injury repair. Together, these studies indicate the presence in adult skeletal muscle of prospectively isolatable muscle-forming stem cells and directly demonstrate the efficacy of myogenic stem cell transplant for treating muscle degenerative disease.
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“Skeletal muscle repair is facilitated by a population of dedicated muscle stem cells (MuSCs), also known as satellite cells, that reside in anatomically defined niches within muscle tissues.”
From The central role of muscle stem cells in regenerative failure with aging (2015) · cites this paper as [6]
In the citing paper
“Subsequently, MuSCs undergo multiple rounds of self-renewing divisions that are essential to their function in regeneration, as demonstrated by transplantation, genetic ablation, and lineage tracing experiments5–12.”
From The central role of muscle stem cells in regenerative failure with aging (2015) · cites this paper as [6]
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“Several groups have reported successful replenishment of the stem cell pool by satellite cell transplantation into dystrophic or irradiated/injured muscles in mice120,139,140, although the rarity of satellite cells in muscle tissue has been a challenge for translating muscle stem cell transplantation to clinical practice141”
From Stem cell aging: mechanisms, regulators and therapeutic opportunities (2014) · cites this paper as [139]
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Metadata
- Authors
- Cerletti, M., Jurga, S., Witczak, C. A., Hirshman, M. F., Shadrach, J. L., Goodyear, L. J., & Wagers, A. J.
- Affiliations
- Joslin Diabetes Center (US)
- Corresponding author
- Wagers, Amy J.
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2008-07
- Volume
- 134
- Issue
- 1
- Pages
- 37-47
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC3665268
- OpenAlex
- W2019428638
- Cited by
- 472
- References
- 49
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 16 · 2023: 14 · 2022: 9 · 2021: 24 · 2020: 31 · 2019: 23 · 2018: 19 · 2017: 18 · 2016: 29 · 2015: 29 · 2014: 33 · 2013: 39 · 2012: 46
- FWCI
- 18.26
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK068626)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (F32AR051663)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Genetics (clinical) › Neurogenetic and Muscular Disorders Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Keywords
- skeletal muscle stem cells, satellite cells, dystrophic muscle, mdx mice, dystrophin deficiency, cell transplantation, muscle regeneration, stem cell heterogeneity, stem cell engraftment
- MeSH terms
- Animals, Cell Separation, Humans, Membrane Proteins, Mice, Inbred C57BL, Muscle Contraction, Muscular Dystrophy, Animal, Dystrophin, Muscle, Skeletal, Satellite Cells, Skeletal Muscle, Stem Cell Transplantation, Mice, Adult Stem Cells
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