Siglec-H is an IPC-specific receptor that modulates type I IFN secretion through DAP12

Amanda L. Blasius, Marina Cella, Jorge Maldonado, Toshiyuki Takai, Marco Colonna

Research output: Contribution to journalArticle

189 Scopus citations

Abstract

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 (Ig)-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.

Original languageEnglish
Pages (from-to)2474-2476
Number of pages3
JournalBlood
Volume107
Issue number6
DOIs
StatePublished - Mar 15 2006

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