Signaling by Myeloid C-Type Lectin Receptors in Immunity and Homeostasis

被引:381
作者
Sancho, David [1 ]
Reis e Sousa, Caetano [2 ]
机构
[1] CNIC, Ctr Nacl Invest Cardiovascu, Dept Vasc Biol & Inflammat, E-28029 Madrid, Spain
[2] Canc Res UK, Immunobiol Lab, London Res Inst, Lincolns Inn Fields Labs, London WC2A 3LY, England
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 30 | 2012年 / 30卷
基金
欧洲研究理事会;
关键词
C-type lectins; innate immunity; endocytosis; pattern recognition; myeloid cells; BETA-GLUCAN RECEPTOR; PATTERN-RECOGNITION RECEPTOR; PLASMACYTOID DENDRITIC CELLS; MACROPHAGE MANNOSE RECEPTOR; MARGINAL ZONE MACROPHAGES; MEDIATES ANTIGEN CAPTURE; SYK TYROSINE KINASE; DC-SIGN; MYCOBACTERIUM-TUBERCULOSIS; IN-VIVO;
D O I
10.1146/annurev-immunol-031210-101352
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Myeloid cells are key drivers of physiological responses to pathogen invasion or tissue damage. Members of the C-type lectin receptor (CLR) family stand out among the specialized receptors utilized by myeloid cells to orchestrate these responses. CLR ligands include carbohydrate, protein, and lipid components of both pathogens and self, which variably trigger endocytic, phagocytic, proinflammatory, or anti-inflammatory reactions. These varied outcomes rely on a versatile system for CLR signaling that includes tyrosine-based motifs that recruit kinases, phosphatases, or endocytic adaptors as well as nontyrosine-based signals that modulate the activation of other pathways or couple to the uptake machinery. Here, we review the signaling properties of myeloid CLRs and how they impact the role of myeloid cells in innate and adaptive immunity.
引用
收藏
页码:491 / 529
页数:39
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