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Human dermal CD14(+) cells are a transient population of monocyte-derived macrophages
Open accessAbstract
Dendritic cells (DCs), monocytes, and macrophages are leukocytes with critical roles in immunity and tolerance. The DC network is evolutionarily conserved; the homologs of human tissue CD141(hi)XCR1⁺ CLEC9A⁺ DCs and CD1c⁺ DCs are murine CD103⁺ DCs and CD64⁻ CD11b⁺ DCs. In addition, human tissues also contain CD14⁺ cells, currently designated as DCs, with an as-yet unknown murine counterpart. Here we have demonstrated that human dermal CD14⁺ cells are a tissue-resident population of monocyte-derived macrophages with a short half-life of <6 days. The decline and reconstitution kinetics of human blood CD14⁺ monocytes and dermal CD14⁺ cells in vivo supported their precursor-progeny relationship. The murine homologs of human dermal CD14⁺ cells are CD11b⁺ CD64⁺ monocyte-derived macrophages. Human and mouse monocytes and macrophages were defined by highly conserved gene transcripts, which were distinct from DCs. The demonstration of monocyte-derived macrophages in the steady state in human tissue supports a conserved organization of human and mouse mononuclear phagocyte system.
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“This does indeed happen, for example in the gut or the dermis (53,54).”
From The impact of ageing on monocytes and macrophages (2021) · cites this paper as [54]
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Identification of a novel lymphoid population in the murine epidermis
Almeida, F. F., Tenno, M., Brzostek, J., Li, J. L. Y., Allies, G., Hoeffel, G., See, P., Ng, L. G., Fehling, H. J., Gascoigne, N. R. J., et al. (2015) · Scientific Reports · doi:10.1038/srep12554 · Cited by 19
Self-citationTissue‐resident macrophages — how to humanize our knowledge
Schlitzer, A., & Schultze, J. L. (2016) · Immunology and Cell Biology · doi:10.1038/icb.2016.82 · Cited by 20
Self-citationVaccines for Herpes Simplex: Recent Progress Driven by Viral and Adjuvant Immunology
Sandgren, K. J., Truong, N. R., Smith, J. B., Bertram, K. M., & Cunningham, A. L. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9814-2_2 · Cited by 18
Date, I., Koya, T., Sakamoto, T., Togi, M., Kawaguchi, H., Watanabe, A., Kato, T., & Shimodaira, S. (2020) · Vaccines · doi:10.3390/vaccines9010010 · Cited by 18
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Pericytes in Cutaneous Wound Healing
Morikawa, S., Iribar, H., Gutiérrez‐Rivera, A., Ezaki, T., & Izeta, A. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-16908-4_1 · Cited by 17
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BDCA1+CD14+ Immunosuppressive Cells in Cancer, a Potential Target?
Ee, T. J. V., Acker, H. H. V., van Oorschot, T. G. M., Tendeloo, V. F. V., Smits, E., Bakdash, G., Schreibelt, G., & de Vries, I. J. M. (2018) · Vaccines · doi:10.3390/vaccines6030065 · Cited by 14
Bourdely, P., Petti, L., Khou, S., Meghraoui, A., Elaldi, R., Cazareth, J., Mossadegh‐Keller, N., Boyer, J., Sieweke, M. H., Poissonnet, G., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.903069 · Cited by 13
Liposomes loaded with vitamin D3 induce regulatory circuits in human dendritic cells
Nagy, N. A., Vigario, F. L., Sparrius, R., van Capel, T. M. M., van Ree, R., Tas, S. W., de Vries, I. J. M., Geijtenbeek, T. B. H., Slütter, B., & de Jong, E. C. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1137538 · Cited by 13
Dendritic Cell Maturation Regulates TSPAN7 Function in HIV-1 Transfer to CD4+ T Lymphocytes
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Functional Specialization of Dendritic Cell Subsets
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Prenatal Development and Function of Human Mononuclear Phagocytes
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Self-citationFunctional specialization of short-lived and long-lived macrophage subsets in human tonsils
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CD103+CD11b− salivary gland dendritic cells have antigen cross‐presenting capacity
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Nonlinear optical microscopy for skinin vivo: Basics, development and applications
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Metadata
- Authors
- McGovern, N., Schlitzer, A., Gunawan, M., Jardine, L., Shin, A., Poyner, E., Green, K., Dickinson, R., Wang, X.-N., Low, D., Best, K., Covins, S., Milne, P., Pagan, S., Aljefri, K., Windebank, M., Miranda-Saavedra, D., Larbi, A., Wasan, P. S., Duan, K., Poidinger, M., Bigley, V., Ginhoux, F., Collin, M., & Haniffa, M.
- Affiliations
- Agency for Science, Technology and Research (SG)
- Newcastle University (GB)
- Corresponding author
- Collin, Matthew
- Haniffa, Muzlifah
- ORCID
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2014-09
- Volume
- 41
- Issue
- 3
- Pages
- 465-477
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC4175180
- OpenAlex
- W2144829409
- Cited by
- 281
- References
- 54
- Citations by year
- 2026: 3 · 2025: 12 · 2024: 13 · 2023: 17 · 2022: 11 · 2021: 24 · 2020: 34 · 2019: 32 · 2018: 25 · 2017: 37 · 2016: 31 · 2015: 36 · 2014: 6
- FWCI
- 16.76
- Type
- journal article
- Language
- en
- Update notices
- erratum (2015-02-17)
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Immunity (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Apollo (University of Cambridge) (submittedVersion, cc-by)
- Apollo (cc-by)
- Funders
- Histiocytosis Association
- Wellcome Trust (101155/Z/13/Z, WT088555MA)
- British Skin Foundation
- Leukaemia and Lymphoma Research
- Newcastle University
- AXA Research Fund
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- CD14+ cells, monocyte-derived macrophages, dermal macrophages, monocytes, monocyte-to-macrophage differentiation, tissue-resident macrophages, reticuloendothelial system, CD11b, CD64, dendritic cells, CD1c+ dendritic cells, CD103+ dendritic cells, human-mouse comparison, macrophage turnover
- MeSH terms
- Animals, Cell Differentiation, Cell Movement, Cells, Cultured, Dendritic Cells, Female, Humans, Immunologic Memory, Macrophages, Mice, Transgenic, Skin, T-Lymphocytes, Receptors, IgG, Lipopolysaccharide Receptors, Cell Lineage, CD11b Antigen, Mice
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