Plasmacytoid dendritic cells sense skin injury and promote wound healing through type I interferons.

Détails

ID Serval
serval:BIB_5DD07D2A54A6
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Plasmacytoid dendritic cells sense skin injury and promote wound healing through type I interferons.
Périodique
Journal of Experimental Medicine
Auteur⸱e⸱s
Gregorio J., Meller S., Conrad C., Di Nardo A., Homey B., Lauerma A., Arai N., Gallo R.L., Digiovanni J., Gilliet M.
ISSN
1540-9538 (Electronic)
ISSN-L
0022-1007
Statut éditorial
Publié
Date de publication
2010
Volume
207
Numéro
13
Pages
2921-2930
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Plasmacytoid dendritic cells (pDCs) are specialized type I interferon (IFN-α/β)-producing cells that express intracellular toll-like receptor (TLR) 7 and TLR9 and recognize viral nucleic acids in the context of infections. We show that pDCs also have the ability to sense host-derived nucleic acids released in common skin wounds. pDCs were found to rapidly infiltrate both murine and human skin wounds and to transiently produce type I IFNs via TLR7- and TLR9-dependent recognition of nucleic acids. This process was critical for the induction of early inflammatory responses and reepithelization of injured skin. Cathelicidin peptides, which facilitate immune recognition of released nucleic acids by promoting their access to intracellular TLR compartments, were rapidly induced in skin wounds and were sufficient but not necessary to stimulate pDC activation and type I IFN production. These data uncover a new role of pDCs in sensing tissue damage and promoting wound repair at skin surfaces.
Mots-clé
Amino Acid Sequence, Animals, Cathelicidins/deficiency, Cathelicidins/genetics, Cytokines/genetics, Cytokines/immunology, Dendritic Cells/immunology, Dendritic Cells/metabolism, Female, Humans, Interferon Type I/genetics, Interferon Type I/immunology, Male, Membrane Glycoproteins/deficiency, Membrane Glycoproteins/genetics, Mice, Mice, 129 Strain, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Knockout, Molecular Sequence Data, Myeloid Differentiation Factor 88/deficiency, Myeloid Differentiation Factor 88/genetics, Nucleic Acids/immunology, Nucleic Acids/metabolism, Receptor, Interferon alpha-beta/deficiency, Receptor, Interferon alpha-beta/genetics, Reverse Transcriptase Polymerase Chain Reaction, Skin/immunology, Skin/injuries, Toll-Like Receptor 7/deficiency, Toll-Like Receptor 7/genetics, Wound Healing/immunology
Pubmed
Web of science
Open Access
Oui
Création de la notice
22/03/2012 12:59
Dernière modification de la notice
20/08/2019 14:15
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