BDCA2/FcεRlγ complex signals through a novel BCR-like pathway in human plasmacytoid dendritic cells

被引:124
作者
Cao, Wei
Zhang, Li
Rosen, David B.
Bover, Laura
Watanabe, Gokuran
Bao, Musheng
Lanier, Lewis L.
Liu, Yong-Jun [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Biostat & Appl Math, Houston, TX 77030 USA
[3] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Biomed Sci Grad Program, San Francisco, CA USA
[5] Univ Calif San Francisco, Biomed Sci Grad Program, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94143 USA
关键词
D O I
10.1371/journal.pbio.0050248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dendritic cells are equipped with lectin receptors to sense the extracellular environment and modulate cellular responses. Human plasmacytoid dendritic cells (pDCs) uniquely express blood dendritic cell antigen 2 (BDCA2) protein, a C-type lectin lacking an identifiable signaling motif. We demonstrate here that BDCA2 forms a complex with the transmembrane adapter Fc epsilon Rl gamma. Through pathway analysis, we identified a comprehensive signaling machinery in human pDCs, similar to that which operates downstream of the B cell receptor (BCR), which is distinct from the system involved in T cell receptor (TCR) signaling. BDCA2 crosslinking resulted in the activation of the BCR-like cascade, which potently suppressed the ability of pDCs to produce type I interferon and other cytokines in response to Toll-like receptor ligands. Therefore, by associating with Fc epsilon Rl gamma, BDCA2 activates a novel BCR-like signaling pathway to regulate the immune functions of pDCs.
引用
收藏
页码:2190 / 2200
页数:11
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