Tumor Necrosis Factor-α (TNF-α) Stimulates Chemotactic Response in Mouse Myogenic Cells
Open accessAbstract
Migration of transplanted myogenic cells occurs during both embryogenesis and regeneration of skeletal muscles and is important for successful myoblast transplantation, but little is known about factors that promote chemotaxis of these cells. Tumor necrosis factor-alpha (TNF-alpha) is known to induce chemotactic effect on several cell types. In this study, we investigated its influence on the in vitro and in vivo motility of C2C12 and primary myoblasts. In the in vitro test performed in the blind-well Boyden chambers, we showed that TNF-alpha (50-400 U/ml) significantly enhanced the ability of myogenic cells to migrate. The dose-response curve for this factor was bell shaped, with maximum activity in the 200 U/ml range. In the in vivo test, intramuscular administration of TNF-alpha was performed by an Alzet pump connected to a perforated polyethylene microtube inserted in the tibialis anterior (TA) of CD1 mice. In these experiments, myoblasts were injected under the muscle epimysium. The recipient mice were immunosuppressed with FK506. Our results showed that, 5 days after myoblast transplantation, cells migrated further in the muscles infused with TNF-alpha than in the muscles not exposed to TNF-alpha. TNF-alpha not only has a chemotactic activity but may also modify cell migration via its action on matrix metalloproteinase (MMP) expression. The proteolytic activities of the MMPs secreted in the muscles were thus also assessed by gelatin zymography. The results showed an inc…
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Initially infiltrating M1 macrophages produce chemokines and cytokines (TNF-α, IL-1β, IL-6) that are chemoattractant and mitogenic for muscle progenitor cells, including Pax7+ satellite cells.
“Briefly, a number of studies have shown that the chemokines and cytokines (TNF-α, IL-1β, IL-6) produced by initially infiltrating M1 macrophages are chemoattractant and mitogenic for muscle progenitor cells, including Pax7+ satellite cells [115–119].”
From Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine (2012) · cites this paper as [116]
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- Authors
- Torrente, Y., Fahime, E. E., Caron, N. J., Del Bo, R., Belicchi, M., Pisati, F., Tremblay, J. P., & Bresolin, N.
- Affiliations
- University of Milan (IT)
- Centre hospitalier de l'Université Laval (CA)
- Centro Dino Ferrari, Institute of Clinical Neurology, University of Milan, Milan, Italy
- Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (IT)
- Corresponding author
- Tremblay, J. P.
- Venue
- Cell Transplantation
- Publisher
- SAGE Publications
- Published
- 2003-01
- Volume
- 12
- Issue
- 1
- Pages
- 91-100
- ISSN
- 0963-6897 (ISSN-L)
- 1555-3892
- OpenAlex
- W1572327103
- Cited by
- 97
- References
- 0
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 8 · 2023: 4 · 2022: 3 · 2021: 3 · 2020: 5 · 2019: 1 · 2018: 1 · 2017: 4 · 2016: 4 · 2015: 4 · 2014: 5 · 2013: 6 · 2012: 7
- FWCI
- 1.72
- Type
- journal article
- Language
- en
- Open access
- green
- doaj.org
- Locations
- Cell Transplantation (publishedVersion)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- 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 › Genetics › Neurogenetic and Muscular Disorders Research
- Keywords
- TNF-α, chemotaxis, myoblast migration, myoblast transplantation, skeletal muscle regeneration, matrix metalloproteinases, MMP-2, MMP-9, C2C12 myoblasts, muscle damage, interferon-gamma, interleukins
- MeSH terms
- Animals, Cell Differentiation, Cells, Cultured, Chemotaxis, Dose-Response Relationship, Drug, Immunosuppressive Agents, Mice, Transgenic, Muscular Diseases, Tumor Necrosis Factor-alpha, Lymphocyte Function-Associated Antigen-1, Macrophage-1 Antigen, Cytokines, Tissue Transplantation, Treatment Outcome, Muscle, Skeletal, Matrix Metalloproteinases, Myoblasts, Mice
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