Paired Activating and Inhibitory Immunoglobulin-like Receptors, MAIR-I and MAIR-II, Regulate Mast Cell and Macrophage Activation

Immune responses are regulated by opposing positive and negative signals triggered by the interaction of activating and inhibitory cell surface receptors with their ligands. Here, we describe novel paired activating and inhibitory immunoglobulin-like receptors, designated myeloid-associated immunogl...

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Published inJournal of experimental medicine Vol. 198; no. 2; pp. 223 - 233
Main Authors 大越 靖, 渋谷 和子, 田原 聡子, 本多 伸一郎, 渋谷 彰, Yotsumoto Katsumi, Okoshi Yasushi, Shibuya Kazuko, Yamazaki Satoshi, Tahara-Hanaoka Satoko, Honda Shin-ichiro, Osawa Mitsujiro, Kuroiwa Asato, Matsuda Yoichi, Tenen Daniel G., Iwama Atsushi, Nakauchi Hiromitsu, Shibuya Akira
Format Journal Article
LanguageEnglish
Published United States Rockefeller University Press 21.07.2003
The Rockefeller University Press
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ISSN0022-1007
1540-9538
DOI10.1084/jem.20021825

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Summary:Immune responses are regulated by opposing positive and negative signals triggered by the interaction of activating and inhibitory cell surface receptors with their ligands. Here, we describe novel paired activating and inhibitory immunoglobulin-like receptors, designated myeloid-associated immunoglobulin-like receptor (MAIR) I and MAIR-II, whose extracellular domains are highly conserved by each other. MAIR-I, expressed on the majority of myeloid cells, including macrophages, granulocytes, mast cells, and dendritic cells, contains the tyrosine-based sorting motif and the immunoreceptor tyrosine-based inhibitory motif-like sequences in the cytoplasmic domain and mediates endocytosis of the receptor and inhibition of IgE-mediated degranulation from mast cells. On the other hand, MAIR-II, expressed on subsets of peritoneal macrophages and B cells, associates with the immunoreceptor tyrosine-based activation motif-bearing adaptor DAP12 and stimulates proinflammatory cytokines and chemokine secretions from macrophages. Thus, MAIR-I and MAIR-II play important regulatory roles in cell signaling and immune responses.
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The present address of M. Osawa, A. Iwama, and H. Nakauchi is the Laboratory of Stem Cell Therapy, Center for Experimental Medicine, The Institute of Medical Science, University of Tokyo, Tokyo, 108-8639 Japan.
ISSN:0022-1007
1540-9538
DOI:10.1084/jem.20021825