The many faces of macrophage activation
Abstract
Journal of Leukocyte Biology considers manuscripts of original investigations focusing on the origins, developmental biology, biochemistry and functions of granulocytes, lymphocytes, mononuclear phagocytes, and other cells involved in host defense. These include full-length papers on original research, rapid communications of new discoveries, letters, commentaries, and invited reviews.
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Classical macrophage activation occurs after induction by IFN-γ and exposure to microbial products such as LPS.
“Classical macrophage activation occurs after induction by IFN-γ and exposure to microbial products such as LPS.[122]”
From Foreign body reaction to biomaterials (2008) · cites this paper as [122]
In early wound repair, infiltrating monocytes and resident macrophages acquire a pro-inflammatory M1 phenotype.
“In the early phase of wound repair, upon exposure to pro-inflammatory cytokines, IFNs, microbial products or DAMPs, infiltrating monocytes and resident macrophages are activated and mainly acquire a pro-inflammatory M1 phenotype (Fig. 2) [57].”
From Transition from inflammation to proliferation: a critical step during wound healing (2016) · cites this paper as [57]
The M1 phenotype emerges from macrophage interaction with pro-inflammatory signals such as IFN-g and LPS.
“The 'classically activated' or M1 phenotype emerges as a result of macrophage interaction with pro-inflammatory signals such as Interferon-g (IFN-g) and microbial products such as lipopolysaccharide (LPS) [17].”
From Biomaterial based modulation of macrophage polarization: a review and suggested design principles (2015) · cites this paper as [17]
Macrophages are a heterogeneous cell population with different markers and functions.
“Macrophages, like the monocytes from which they derive, are a heterogeneous cell population each with different markers and functions [1,8–12].”
From Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine (2012) · cites this paper as [11]
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- Authors
- Mosser, D. M.
- Affiliations
- University of Maryland, College Park (US)
- Corresponding author
- Mosser, David M
- ORCID
- Mosser, David M
- Venue
- Journal of Leukocyte Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2003-02-01
- Volume
- 73
- Issue
- 2
- Pages
- 209-212
- ISSN
- 0741-5400 (ISSN-L)
- 1938-3673
- OpenAlex
- W2016293419
- Cited by
- 1,902
- References
- 38
- Citations by year
- 2026: 16 · 2025: 30 · 2024: 57 · 2023: 42 · 2022: 67 · 2021: 76 · 2020: 68 · 2019: 81 · 2018: 65 · 2017: 92 · 2016: 115 · 2015: 111 · 2014: 139 · 2013: 129 · 2012: 133
- FWCI
- 5.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Leukocyte Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Keywords
- macrophage activation, macrophages, mononuclear phagocytes, host defense, granulocytes, lymphocytes, cell development
- MeSH terms
- Animals, Humans, Interferon-gamma, Macrophage Activation, Macrophages, Interleukin-4, Interleukin-10
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