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

被引:278
作者
Gregorio, Josh [1 ,4 ]
Meller, Stephan [1 ]
Conrad, Curdin [1 ]
Di Nardo, Anna [5 ]
Homey, Bernhard [6 ]
Lauerma, Antti [7 ,8 ]
Arai, Naoko [9 ]
Gallo, Richard L. [5 ]
DiGiovanni, John [10 ]
Gilliet, Michel [1 ,2 ,3 ,4 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Melanoma Med Oncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Dermatol, Houston, TX 77030 USA
[4] Univ Texas Houston, Grad Sch Biomed Sci, Houston, TX 77030 USA
[5] Univ Calif San Diego, Div Dermatol, La Jolla, CA 92093 USA
[6] Univ Dusseldorf, Dept Dermatol, D-40225 Dusseldorf, Germany
[7] Finnish Inst Occupat Hlth, FIN-00250 Helsinki, Finland
[8] Univ Helsinki, Cent Hosp, Skin & Allergy Hosp, FIN-00290 Helsinki, Finland
[9] SBI Biotech Co Ltd, Ginkgo Biomed Res Inst, Kawasaki, Kanagawa 2160001, Japan
[10] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
关键词
TOLL-LIKE RECEPTORS; MEMORY T-CELLS; ANTIMICROBIAL PEPTIDE; SIGNALING PATHWAY; NUCLEIC-ACIDS; HUMAN BLOOD; SELF-DNA; PSORIASIS; INFLAMMATION; PRECURSORS;
D O I
10.1084/jem.20101102
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Plasmacytoid dendritic cells (pDCs) are specialized type I interferon (IFN-alpha/beta)-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.
引用
收藏
页码:2921 / 2930
页数:10
相关论文
共 55 条
[1]   Targeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function [J].
Adachi, O ;
Kawai, T ;
Takeda, K ;
Matsumoto, M ;
Tsutsui, H ;
Sakagami, M ;
Nakanishi, K ;
Akira, S .
IMMUNITY, 1998, 9 (01) :143-150
[2]   Chemerin expression marks early psoriatic skin lesions and correlates with plasmacytoid dendritic cell recruitment [J].
Albanesi, Cristina ;
Scarponi, Claudia ;
Pallotta, Sabatino ;
Daniele, Roberta ;
Bosisio, Daniela ;
Madonna, Stefania ;
Fortugno, Paola ;
Gonzalvo-Feo, Safiye ;
Franssen, Jean-Denis ;
Parmentier, Marc ;
De Pita, Ornella ;
Girolomoni, Giampiero ;
Sozzani, Silvano .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (01) :249-258
[3]   Nucleic acids of mammalian origin can act as endogenous ligands for toll-like receptors and may promote systemic lupus erythematosus [J].
Barrat, FJ ;
Meeker, T ;
Gregorio, J ;
Chan, JH ;
Uematsu, S ;
Akira, S ;
Chang, B ;
Duramad, O ;
Coffman, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (08) :1131-1139
[4]   Bone marrow stromal cell antigen 2 is a specific marker of type IIFN-producing cells in the naive mouse, but a promiscuous cell surface antigen following IFN stimulation [J].
Blasius, Amanda L. ;
Giurisato, Emanuele ;
Celia, Marina ;
Schreiber, Robert D. ;
Shaw, Andrey S. ;
Colonna, Marco .
JOURNAL OF IMMUNOLOGY, 2006, 177 (05) :3260-3265
[5]   IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes [J].
Boniface, K ;
Bernard, FX ;
Garcia, M ;
Gurney, AL ;
Lecron, JC ;
Morel, F .
JOURNAL OF IMMUNOLOGY, 2005, 174 (06) :3695-3702
[6]   Plasmacytoid monocytes migrate to inflamed lymph nodes and produce large amounts of type I interferon [J].
Cella, M ;
Jarrossay, D ;
Facchetti, F ;
Alebardi, O ;
Nakajima, H ;
Lanzavecchia, A ;
Colonna, M .
NATURE MEDICINE, 1999, 5 (08) :919-923
[7]   Toll-like receptor 7 and TLR9 dictate autoantibody specificity and have opposing inflammatory and regulatory roles in a murine model of lupus [J].
Christensen, Sean R. ;
Shupe, Jonathan ;
Nickerson, Kevin ;
Kashgarian, Michael ;
Flavell, Richard A. ;
Shlomchik, Mark J. .
IMMUNITY, 2006, 25 (03) :417-428
[8]   Innate antiviral responses by means of TLR7-mediated recognition of single-stranded RNA [J].
Diebold, SS ;
Kaisho, T ;
Hemmi, H ;
Akira, S ;
Sousa, CRE .
SCIENCE, 2004, 303 (5663) :1529-1531
[9]   Role for Plasmacytoid Dendritic Cells in the Immune Control of Recurrent Human Herpes Simplex Virus Infection [J].
Donaghy, Heather ;
Bosnjak, Lidija ;
Harman, Andrew N. ;
Marsden, Valerie ;
Tyring, Stephen K. ;
Meng, Tze-Chiang ;
Cunningham, Anthony L. .
JOURNAL OF VIROLOGY, 2009, 83 (04) :1952-1961
[10]   Cutaneous injury induces the release of cathelicidin anti-microbial peptides active against group A Streptococcus [J].
Dorschner, RA ;
Pestonjamasp, VK ;
Tamakuwala, S ;
Ohtake, T ;
Rudisill, J ;
Nizet, V ;
Agerberth, B ;
Gudmundsson, GH ;
Gallo, RL .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (01) :91-97