The role and function of Fcγ receptors on myeloid cells
Open accessAbstract
A key determinant for the survival of organisms is their capacity to recognize and respond efficiently to foreign antigens. This is largely accomplished by the orchestrated activity of the innate and adaptive branches of the immune system. Antibodies are specifically generated in response to foreign antigens, facilitating thereby the specific recognition of antigens of almost infinite diversity. Receptors specific for the Fc domain of antibodies, Fc receptors, are expressed on the surface of the various myeloid leukocyte populations and mediate the binding and recognition of antibodies by innate leukocytes. By directly linking the innate and the adaptive components of immunity, Fc receptors play a central role in host defense and the maintenance of tissue homeostasis through the induction of diverse proinflammatory, anti-inflammatory, and immunomodulatory processes that are initiated upon engagement by the Fc domain. In this chapter, we discuss the mechanisms that regulate Fc domain binding to the various types of Fc receptors and provide an overview of the astonishing diversity of effector functions that are mediated through Fc-FcR interactions on myeloid cells. Lastly, we discuss the impact of FcR-mediated interactions in the context of IgG-mediated inflammation, autoimmunity, susceptibility to infection, and responsiveness to antibody-based therapeutics.
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Phagocytosis-related genes FCER1G, FCGR2A, TYROBP, and GAS6 are down-regulated in AD monocytes compared with AC monocytes, indicating a reduced ability of AD monocytes to phagocytose Aβ.
“We found that the expression of phagocytosis-related genes, including FCER1G, FCGR2A, TYROBP, and GAS6 (46–48), was down-regulated in AD monocytes as compared to AC monocytes (Fig. 3C), indicating a reduced ability of AD monocytes to phagocytose Aβ.”
From Understanding monocyte-driven neuroinflammation in Alzheimer’s disease using human cortical organoid microphysiological systems (2025) · cites this paper as [46]
The sections on FcγR types and on Phagocytosis and Antigen Presentation (page unavailable) identify FCER1G as encoding an Fc-receptor signaling chain, FCGR2A as encoding FcγRIIa, and Fcγ receptors as mediators of phagocytosis. The citation is attached to the description of the genes as phagocytosis-related, not to the citing authors’ own finding of down-regulation. Our copy does not establish that TYROBP or GAS6 are phagocytosis-related, so it supports only part of the cited gene list. (LLM, conf=0.86)
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Pathogenesis of Lupus Nephritis
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- Authors
- Bournazos, S., Wang, T. T., & Ravetch, J. V.
- Affiliations
- Rockefeller University (US)
- Corresponding author
- Ravetch, Jeffrey V.
- Venue
- Microbiology Spectrum
- Publisher
- American Society for Microbiology
- Published
- 2016-12-23
- Volume
- 4
- Issue
- 6
- ISSN
- 2165-0497 (ISSN-L)
- PMC
- PMC5240797
- OpenAlex
- W2594777914
- Cited by
- 138
- References
- 219
- Citations by year
- 2026: 14 · 2025: 12 · 2024: 13 · 2023: 10 · 2022: 20 · 2021: 20 · 2020: 20 · 2019: 20 · 2018: 8 · 2017: 1
- FWCI
- 8.39
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Microbiology Spectrum (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Bill and Melinda Gates Foundation
- National Institutes of Health
- Defense Advanced Research Projects Agency
- National Cancer Institute (P01CA190174, R35CA196620)
- National Institute of Allergy and Infectious Diseases (U19AI109946, U19AI111825, P01AI100148)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- Fc gamma receptor, myeloid cells, Fc receptor binding, innate immunity, adaptive immunity, autoimmunity, infection susceptibility, therapeutic antibodies, immunomodulation, innate-adaptive immune crosstalk
- MeSH terms
- Animals, Antibodies, Humans, Immunity, Innate, Protein Binding, Receptors, IgG, Myeloid Cells, Adaptive Immunity
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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