Characterization of Leukocyte Mono-immunoglobulin-like Receptor 7 (LMIR7)/CLM-3 as an Activating Receptor

• Published in: The Journal of biological chemistry Vol. 285; no. 46; pp. 35274 - 35283
• Main Authors: Enomoto, Yutaka, Yamanishi, Yoshinori, Izawa, Kumi, Kaitani, Ayako, Takahashi, Mariko, Maehara, Akie, Oki, Toshihiko, Takamatsu, Reiko, Kajikawa, Masunori, Takai, Toshiyuki, Kitamura, Toshio, Kitaura, Jiro
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01.11.2010
• Subjects: Cell Surface Receptor; FcRγ; Immunology; Innate Immunity; Leukocyte; Paired Receptor; Receptor Structure-Function; Receptors; Receptor Structure-Function; Receptors; Immunology; Leukocyte; Paired Receptor; Innate Immunity; Cell Surface Receptor; FcRγ
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M110.137166

Here we characterize leukocyte mono-Ig-like receptor 7 (LMIR7)/CLM-3 and compare it with an activating receptor, LMIR4/CLM-5, that is a counterpart of an inhibitory receptor LMIR3/CLM-1. LMIR7 shares high homology with LMIR4 in the amino acid sequences of its Ig-like and transmembrane domains. Flow cytometric analysis demonstrated that LMIR4 was predominantly expressed in neutrophils, whereas LMIR7 was highly expressed in mast cells and monocytes/macrophages. Importantly, LMIR7 engagement induced cytokine production in bone marrow-derived mast cells (BMMCs). Although FcRγ deficiency did not affect surface expression levels of LMIR7, it abolished LMIR7-mediated activation of BMMCs. Consistently we found significant interaction of LMIR7-FcRγ, albeit with lower affinity compared with that of LMIR4-FcRγ. Our results showed that LMIR7 transmits an activating signal through interaction with FcRγ. In addition, like LMIR4, LMIR7 synergizes with TLR4 in signaling. Analysis of several chimera receptors composed of LMIR4 and LMIR7 revealed these findings: 1) the transmembrane of LMIR7 with no charged residues maintained its surface expression at high levels in the absence of FcRγ; 2) the extracellular juxtamembrane region of LMIR7 had a negative effect on its surface expression levels; and 3) the strong interaction of LMIR4 with FcRγ depended on the extracellular juxtamembrane region as well as the transmembrane domain of LMIR4. Thus, LMIR7 shares similarities with LMIR4, although they are differentially regulated in their distribution, expression, and function.