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Human dermal CD14⁺ cells are a transient population of monocyte-derived macrophages.

Published version
Peer-reviewed

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Authors

Schlitzer, Andreas 
Gunawan, Merry 
Jardine, Laura 
Shin, Amanda 

Abstract

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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Keywords

Animals, CD11b Antigen, Cell Differentiation, Cell Lineage, Cell Movement, Cells, Cultured, Dendritic Cells, Female, Humans, Immunologic Memory, Lipopolysaccharide Receptors, Macrophages, Mice, Mice, Transgenic, Receptors, IgG, Skin, T-Lymphocytes

Journal Title

Immunity

Conference Name

Journal ISSN

1074-7613
1097-4180

Volume Title

41

Publisher

Elsevier BV