Re-evaluation of human BDCA-2(+) DC during acute sterile skin inflammation

Plasmacytoid dendritic cells (pDCs) produce type I interferon (IFN-I) and are traditionally defined as being BDCA-2(+)CD123(+). pDCs are not readily detectable in healthy human skin, but have been suggested to accumulate in wounds. Here, we describe a CD1a-bearing BDCA-2(+)CD123(int) DC subset that...

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Veröffentlicht in:The Journal of experimental medicine 2020-03, Vol.217 (3)
Hauptverfasser: Chen, Yi-Ling, Gomes, Tomas, Hardman, Clare S., Braga, Felipe A. Vieira, Gutowska-Owsiak, Danuta, Salimi, Maryam, Gray, Nicki, Duncan, David A., Reynolds, Gary, Johnson, David, Salio, Mariolina, Cerundolo, Vincenzo, Barlow, Jillian L., McKenzie, Andrew N. J., Teichmann, Sarah A., Haniffa, Muzlifah, Ogg, Graham
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Sprache:eng
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Zusammenfassung:Plasmacytoid dendritic cells (pDCs) produce type I interferon (IFN-I) and are traditionally defined as being BDCA-2(+)CD123(+). pDCs are not readily detectable in healthy human skin, but have been suggested to accumulate in wounds. Here, we describe a CD1a-bearing BDCA-2(+)CD123(int) DC subset that rapidly infiltrates human skin wounds and comprises a major DC population. Using single-cell RNA sequencing, we show that these cells are largely activated DCs acquiring features compatible with lymph node homing and antigen presentation, but unexpectedly express both BDCA-2 and CD123, potentially mimicking pDCs. Furthermore, a third BDCA-2-expressing population, Axl(+)Siglec-6(+) DCs (ASDC), was also found to infiltrate human skin during wounding. These data demonstrate early skin infiltration of a previously unrecognized CD123(int)BDCA-2(+)CD1a(+)DC subset during acute sterile inflammation, and prompt a re-evaluation of previously ascribed pDC involvement in skin disease.
ISSN:0022-1007
1540-9538
DOI:10.1084/jem.20190811