共 21 条
Siglec-H is an IPC-specific receptor that modulates type IIFN secretion through DAP12
被引:218
作者:

Blasius, AL
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机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA

Cella, M
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机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA

Maldonado, J
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机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA

Takai, T
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机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA

Colonna, M
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机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
机构:
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Tohoku Univ, Dept Expt Immunol, Inst Dev Aging & Canc, Sendai, Miyagi 980, Japan
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D O I:
10.1182/blood-2005-09-3746
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Natural interferon (IFN)-producing cells are the primary cell type responsible for production of type I IFN in response to viruses. Herein we report the identification of the first molecular marker of mouse natural interferon-producing cells (IPCs), a novel member of the sialic acid-binding immunoglobulin (lg)-like lectin (Siglec) family termed Siglec-H. Siglec-H is expressed exclusively on IPCs and is unique among Siglec proteins in that it associates with the adaptor protein DAP12. Moreover, we show that DAP12 modulates the type I IFN response of IPCs to a Toll-like receptor 9 (TLR9) agonist. This observation explains our previous finding that stimulation of IPCs with 440c, a Siglec-H-specific antibody, reduces IPC secretion of type I IFN. Moreover, it supports a model in which engagement of DNAX-activation protein 12 (DAP12)associated receptors with antibodies or low avidity endogenous ligands interferes with TLR-mediated cellular activation.
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页码:2474 / 2476
页数:3
相关论文
共 21 条
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