Integrin signaling in neutrophils and macrophages uses adaptors containing immunoreceptor tyrosine-based activation motifs

Attila Mócsai, Clare L. Abram, Zoltán Jakus, Yongmei Hu, Lewis L. Lanier, Clifford A. Lowell

Research output: Contribution to journalArticle

249 Citations (Scopus)

Abstract

At sites of inflammation, ligation of leukocyte integrins is critical for the activation of cellular effector functions required for host defense. However, the signaling pathways linking integrin ligation to cellular responses are poorly understood. Here we show that integrin signaling in neutrophils and macrophages requires adaptors containing immunoreceptor tyrosine-based activation motifs (ITAMs). Neutrophils and macrophages lacking two ITAM-containing adaptor proteins, DAP12 and FcRγ, were defective in integrin-mediated responses. Activation of the tyrosine kinase Syk by integrins required that DAP12 and FcRγ were first phosphorylated by Src family kinases. Retroviral transduction of neutrophils and macrophages with wild-type and mutant Syk or DAP12 demonstrated that the Src homology 2 domains of Syk and the ITAM of DAP12 were required for integrin signaling. Our data show that integrin signaling for the activation of cellular responses in neutrophils and macrophages proceeds by an immunoreceptor-like mechanism.

Original languageEnglish
Pages (from-to)1326-1333
Number of pages8
JournalNature Immunology
Volume7
Issue number12
DOIs
Publication statusPublished - Dec 1 2006

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ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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