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Review
. 2014 Nov;262(1):25-35.
doi: 10.1111/imr.12215.

Origin, development, and homeostasis of tissue-resident macrophages

Affiliations
Review

Origin, development, and homeostasis of tissue-resident macrophages

Malay Haldar et al. Immunol Rev. 2014 Nov.

Abstract

Macrophages are versatile cells of the hematopoietic system that display remarkable functional diversity encompassing innate immune responses, tissue development, and tissue homeostasis. Macrophages are present in almost all tissues of the body and display distinct location-specific phenotypes and gene expression profiles. Recent studies also demonstrate distinct origins of tissue-resident macrophages. This emerging picture of ontological, functional, and phenotypic heterogeneity within tissue macrophages has altered our understanding of these cells, which play important roles in many human diseases. In this review, we discuss the different origins of tissue macrophages, the transcription factors regulating their development, and the mechanisms underlying their homeostasis at steady state.

Keywords: cell differentiation; immune system ontogeny; lineage commitment; monocytes/macrophages.

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Conflict of interest statement

The authors have no conflicts of interest to declare.

Figures

Fig. 1
Fig. 1. Embryonic and postnatal origins of tissue-resident macrophages
Macrophages are color coded to indicate origin. Arrows connecting macrophages indicate persistence into postnatal phase.

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References

    1. Metchnikoff E. Leçons sur la pathologie comparée de l’inflammation. Masson. 1892
    1. Austyn JM, Gordon S. F4/80, a monoclonal antibody directed specifically against the mouse macrophage. Eur. J. Immunol. 1981;11:805–815. - PubMed
    1. Holness CL, Simmons DL. Molecular cloning of CD68, a human macrophage marker related to lysosomal glycoproteins. Blood. 1993;81:1607–1613. - PubMed
    1. Gordon S, Hamann J, Lin H-H, Stacey M. F4/80 and the related adhesion-GPCRs. Eur. J. Immunol. 2011;41:2472–2476. - PubMed
    1. Taylor PR, Martinez-Pomares L, Stacey M, Lin H-H, Brown GD, Gordon S. Macrophage receptors and immune recognition. Annu. Rev. Immunol. 2005;23:901–944. - PubMed

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