Human Dermal CD14+ Cells Are a Transient Population of Monocyte-Derived Macrophages

نویسندگان

  • Naomi McGovern
  • Andreas Schlitzer
  • Merry Gunawan
  • Laura Jardine
  • Amanda Shin
  • Elizabeth Poyner
  • Kile Green
  • Rachel Dickinson
  • Xiao-nong Wang
  • Donovan Low
  • Katie Best
  • Samuel Covins
  • Paul Milne
  • Sarah Pagan
  • Khadija Aljefri
  • Martin Windebank
  • Diego Miranda Saavedra
  • Anis Larbi
  • Pavandip Singh Wasan
  • Kaibo Duan
  • Michael Poidinger
  • Venetia Bigley
  • Florent Ginhoux
  • Matthew Collin
  • Muzlifah Haniffa
چکیده

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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عنوان ژورنال:

دوره 41  شماره 

صفحات  -

تاریخ انتشار 2014