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Mechanisms of Organ Injury and Repair by Macrophages
Open accessAbstract
Macrophages regulate tissue regeneration following injury. They can worsen tissue injury by producing reactive oxygen species and other toxic mediators that disrupt cell metabolism, induce apoptosis, and exacerbate ischemic injury. However, they also produce a variety of growth factors, such as IGF-1, VEGF-α, TGF-β, and Wnt proteins that regulate epithelial and endothelial cell proliferation, myofibroblast activation, stem and tissue progenitor cell differentiation, and angiogenesis. Proresolving macrophages in turn restore tissue homeostasis by functioning as anti-inflammatory cells, and macrophage-derived matrix metalloproteinases regulate fibrin and collagen turnover. However, dysregulated macrophage function impairs wound healing and contributes to the development of fibrosis. Consequently, the mechanisms that regulate these different macrophage activation states have become active areas of research. In this review, we discuss the common and unique mechanisms by which macrophages instruct tissue repair in the liver, nervous system, heart, lung, skeletal muscle, and intestine and illustrate how macrophages might be exploited therapeutically.
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“The relative quantification of CD68 and CD163 proteins roughly distinguishes the activation of M1 and M2 macrophages (Vannella and Wynn, 2017;Huang et al., 2018;Kim et al., 2019).”
From Nanosilver alleviates foreign body reaction and facilitates wound repair by regulating macrophage polarization (2023) · cites this paper as Vannella and Wynn, 2017
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“pro-fibrotic macrophages commonly coordinate scar formation via a range of interactions with fibroblasts, the major cellular source of pathological extracellular matrix deposition during fibrosis18,27,74–78.”
From Fibrosis: from mechanisms to medicines (2020) · cites this paper as [77]
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“Previous work has shown that proximity is crucial to allow crosstalk between macrophages and contractile fibroblasts27,77,78”
From Fibrosis: from mechanisms to medicines (2020) · cites this paper as [77]
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Metadata
- Authors
- Vannella, K. M., & Wynn, T. A.
- Affiliations
- National Institutes of Health (US)
- Venue
- Annual Review of Physiology
- Publisher
- Annual Reviews
- Published
- 2017-02-10
- Volume
- 79
- Issue
- 1
- Pages
- 593-617
- ISSN
- 0066-4278 (ISSN-L)
- 1545-1585
- OpenAlex
- W2467677013
- Semantic Scholar
- 00554bdce4ebdeef31bcb674e3634efc26188db4
- Cited by
- 656
- References
- 127
- Citations by year
- 2026: 52 · 2025: 76 · 2024: 102 · 2023: 78 · 2022: 89 · 2021: 73 · 2020: 66 · 2019: 60 · 2018: 41 · 2017: 19
- FWCI
- 5.07
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annual Review of Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases
- Topics
- Health Sciences › Medicine › Surgery › Wound Healing and Treatments
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Keywords
- macrophages, tissue repair, tissue regeneration, wound healing, macrophage polarization, reactive oxygen species, apoptosis, growth factors, angiogenesis, myofibroblast activation, matrix metalloproteinases, fibrosis, liver, nervous system, heart, lung, skeletal muscle, intestine, anti-inflammatory macrophages
- MeSH terms
- Animals, Cell Differentiation, Homeostasis, Humans, Macrophages, Regeneration, Wound Healing
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