Regulation of PDGF and its receptors in fibrotic diseases
Abstract
Platelet-derived growth factor (PDGF) isoforms play a major role in stimulating the replication, survival, and migration of myofibroblasts during the pathogenesis of fibrotic diseases. During fibrogenesis, PDGF is secreted by a variety of cell types as a response to injury, and many pro-inflammatory cytokines mediate their mitogenic effects via the autocrine release of PDGF. PDGF action is determined by the relative expression of PDGF alpha-receptors (PDGFRalpha) and beta-receptors (PDGFRbeta) on the surface of myofibroblasts. These receptors are induced during fibrogenesis, thereby amplifying biological responses to PDGF isoforms. PDGF action is also modulated by extracellular binding proteins and matrix molecules. This review summarizes the literature on the role of PDGF and its receptors in the development of fibrosis in a variety of organ systems, including lung, liver, kidney, and skin.
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PDGF released by macrophages induces proliferation of myofibroblasts, which over time cover the entire surface of the implant.
“PDGF—also released by macrophages—induces the proliferation of myofibroblasts, which over time cover the entire surface of the implant (Bonner, 2004).”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Bonner, 2004
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Hayes, B. J., Riehle, K. J., Shimizu-Albergine, M., Bauer, R. L., Hudkins, K. L., Johansson, F., Yeh, M. M., Mahoney, W. M., Yeung, R. S., & Campbell, J. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092925 · Cited by 59 · see citing works
Protective effect of EX-527 against high-fat diet-induced diabetic nephropathy in Zucker rats
Kundu, A., Richa, S., Dey, P., Kim, K. S., Son, J. Y., Kim, H. R., Lee, S.-Y., Lee, B.-H., Lee, K. Y., Kacew, S., et al. (2020) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2020.114899 · Cited by 27 · see citing works
Drugs of the future for Peyronie’s disease
Gur, S., Kadowitz, P. J., & Hellstrom, W. J. G. (2012) · Medical Hypotheses · doi:10.1016/j.mehy.2011.11.008 · Cited by 10 · see citing works
- Authors
- Bonner, J. C.
- Affiliations
- National Institute of Environmental Health Sciences (US)
- Corresponding author
- Bonner, James C
- ORCID
- Bonner, James C
- Venue
- Cytokine & Growth Factor Reviews
- Publisher
- Elsevier BV
- Published
- 2004-08
- Volume
- 15
- Issue
- 4
- Pages
- 255-273
- ISSN
- 1359-6101 (ISSN-L)
- OpenAlex
- W2002999999
- Cited by
- 768
- References
- 190
- Citations by year
- 2026: 29 · 2025: 29 · 2024: 29 · 2023: 29 · 2022: 26 · 2021: 42 · 2020: 38 · 2019: 41 · 2018: 32 · 2017: 43 · 2016: 47 · 2015: 41 · 2014: 44 · 2013: 39 · 2012: 56
- FWCI
- 3.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cytokine & Growth Factor Reviews (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Keywords
- platelet-derived growth factor, PDGF receptor, PDGFRA, PDGFRβ, fibrosis, fibrogenesis, myofibroblasts, autocrine signaling, inflammatory cytokines, extracellular matrix, pulmonary fibrosis, liver fibrosis, renal fibrosis, skin fibrosis
- MeSH terms
- Animals, Fibroblasts, Fibrosis, Gene Expression Regulation, Humans, Inflammation, Interleukin-1, Kidney, Liver, Lung, Models, Biological, Muscles, Platelet-Derived Growth Factor, Scleroderma, Systemic, Tissue Distribution, Signal Transduction, Transforming Growth Factor beta, Protein Isoforms, Receptor, Platelet-Derived Growth Factor alpha, Receptor, Platelet-Derived Growth Factor beta, Transforming Growth Factor beta1
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