The DOI matches its Crossref record; 115 of the 116 references it cites were found in a registry or an index.
Origin and Functions of Tissue Macrophages
Open accessAbstract
Macrophages are distributed in tissues throughout the body and contribute to both homeostasis and disease. Recently, it has become evident that most adult tissue macrophages originate during embryonic development and not from circulating monocytes. Each tissue has its own composition of embryonically derived and adult-derived macrophages, but it is unclear whether macrophages of distinct origins are functionally interchangeable or have unique roles at steady state. This new understanding also prompts reconsideration of the function of circulating monocytes. Classical Ly6c(hi) monocytes patrol the extravascular space in resting organs, and Ly6c(lo) nonclassical monocytes patrol the vasculature. Inflammation triggers monocytes to differentiate into macrophages, but whether resident and newly recruited macrophages possess similar functions during inflammation is unclear. Here, we define the tools used for identifying the complex origin of tissue macrophages and discuss the relative contributions of tissue niche versus ontological origin to the regulation of macrophage functions during steady state and inflammation.
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“Macrophages often are the first immune cells that encounter invading pathogens [219,220,221].”
From Functions of ROS in Macrophages and Antimicrobial Immunity (2021) · cites this paper as [220]
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Macrophage activation and polarization: nomenclature and experimental guidelines
Murray, P. J., Allen, J. E., Biswas, S. K., Fisher, E. A., Gilroy, D. W., Goerdt, S., Gordon, S., Hamilton, J. A., Ivashkiv, L. B., Lawrence, T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.008 · Cited by 6,337
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
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Macrophage biology in development, homeostasis and disease
Wynn, T. A., Chawla, A., & Pollard, J. W. (2013) · Nature · doi:10.1038/nature12034 · Cited by 4,684 · cited 1×
“Several detailed review articles describing different aspects of macrophage ontogeny and function have been published (Sieweke and Allen, 2013; Davies et al., 2013a; Wynn et al., 2013).”
BackgroundSynaptic Pruning by Microglia Is Necessary for Normal Brain Development
Paolicelli, R. C., Bolasco, G., Pagani, F., Maggi, L., Scianni, M., Panzanelli, P., Giustetto, M., Ferreira, T. A., Guiducci, E., Dumas, L., et al. (2011) · Science · doi:10.1126/science.1202529 · Cited by 4,244
The Classical Complement Cascade Mediates CNS Synapse Elimination
Stevens, B., Allen, N. J., Vazquez, L. E., Howell, G. R., Christopherson, K. S., Nouri, N., Micheva, K. D., Mehalow, A. K., Huberman, A. D., Stafford, B., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.036 · Cited by 3,313
Fate Mapping Reveals Origins and Dynamics of Monocytes and Tissue Macrophages under Homeostasis
Yona, S., Kim, K.-W., Wolf, Y., Mildner, A., Varol, D., Breker, M., Strauss-Ayali, D., Viukov, S., Guilliams, M., Misharin, A., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.12.001 · Cited by 3,245
TREM2 Variants in Alzheimer's Disease
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Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor
Parkhurst, C. N., Yang, G., Ninan, I., Savas, J. N., Yates, J. R., Lafaille, J. J., Hempstead, B. L., Littman, D. R., & Gan, W.-B. (2013) · Cell · doi:10.1016/j.cell.2013.11.030 · Cited by 2,599
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Defining Cardiac Recovery at Single Cell Resolution
Amrute, J. M., Lai, L., Ma, P., Koenig, A. L., Kamimoto, K., Bredemeyer, A., Shankar, T. S., Kuppe, C., Kadyrov, F. F., Schulte, L. J., et al. (2022) · doi:10.1101/2022.09.11.507463 · Cited by 6
Self-citationCarrier, M., Robert, M.-È., St-Pierre, M.-K., Ibáñez, F. G., Gonçalves de Andrade, E., Laroche, A., Picard, K., Vecchiarelli, H. A., Savage, J. C., Boilard, É., et al. (2024) · iScience · doi:10.1016/j.isci.2024.110037 · Cited by 5
Wnt Signaling Regulates Macrophage Mediated Immune Response to Pathogens
Jati, S., & Sen, M. (2020) · Macrophage Activation - Biology and Disease · doi:10.5772/intechopen.86433 · Cited by 4
Metadata
- Authors
- Epelman, S., Lavine, K. J., & Randolph, G. J.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Epelman, Slava
- Randolph, Gwendalyn J.
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2014-07
- Volume
- 41
- Issue
- 1
- Pages
- 21-35
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC4470379
- OpenAlex
- W2054540776
- Cited by
- 1,585
- References
- 116
- Citations by year
- 2026: 95 · 2025: 127 · 2024: 152 · 2023: 127 · 2022: 197 · 2021: 168 · 2020: 140 · 2019: 143 · 2018: 138 · 2017: 102 · 2016: 94 · 2015: 89 · 2014: 13
- FWCI
- 9.69
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (R01AI049653)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Keywords
- tissue macrophages, macrophage origin, embryonic development, monocyte-derived macrophages, Ly6C+ monocytes, non-classical monocytes, tissue niche, macrophage function, inflammation, macrophage heterogeneity
- MeSH terms
- Animals, Antigens, Ly, Cell Differentiation, Central Nervous System, Humans, Inflammation, Lung, Macrophages, Monocytes, Myocardium, Cell Lineage, Mice
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