Siglec-8 - A novel eosinophil-specific member of the immunoglobulin superfamily

被引:167
作者
Floyd, H
Ni, J
Cornish, AL
Zeng, ZZ
Liu, D
Carter, KC
Steel, J
Crocker, PR [1 ]
机构
[1] Univ Dundee, Dept Biochem, Wellcome Trust Bioctr, Dundee DD1 5EH, Scotland
[2] Human Genome Sci Inc, Rockville, MD 20852 USA
[3] Imperial Canc Res Fund, London WC1, England
关键词
D O I
10.1074/jbc.275.2.861
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe the characterization of siglec-8, a novel sialic acid-binding immunoglobulin-like lectin that is expressed specifically by eosinophils. A full-length cDNA encoding siglec-8 was isolated from a human eosinophil cDNA library. Siglec-8 is predicted to contain three extracellular immunoglobulin-like domains, a transmembrane region, and a cytoplasmic tail of 47 amino acids. The siglec-8 gene mapped on chromosome 19q13.33-41, closely linked to genes encoding CD33 (siglec-3), siglec-5, siglec-6, and siglec-7. When siglec-8 was expressed on COS cells or as a recombinant protein fused to the Fc region of human IgG(1), it was able to mediate sialic acid-dependent binding to human erythrocytes and to soluble sialoglycoconjugates. Using specific monoclonal antibodies, siglec-8 could be detected only on eosinophils and hence appears to be the first example of an eosinophil-specific transmembrane receptor.
引用
收藏
页码:861 / 866
页数:6
相关论文
共 28 条
[1]   The pathobiology of eosinophilic inflammation [J].
Boyce, JA .
ALLERGY AND ASTHMA PROCEEDINGS, 1997, 18 (05) :293-300
[2]   Characterization of siglec-5, a novel glycoprotein expressed on myeloid cells related to CD33 [J].
Cornish, AL ;
Freeman, S ;
Forbes, G ;
Ni, J ;
Zhang, M ;
Cepeda, M ;
Gentz, R ;
Augustus, M ;
Carter, KC ;
Crocker, PR .
BLOOD, 1998, 92 (06) :2123-2132
[3]  
Crocker P R, 1998, Glycobiology, V8, pv
[4]   SIALOADHESIN, A MACROPHAGE SIALIC-ACID BINDING-RECEPTOR FOR HEMATOPOIETIC-CELLS WITH 17 IMMUNOGLOBULIN-LIKE DOMAINS [J].
CROCKER, PR ;
MUCKLOW, S ;
BOUCKSON, V ;
MCWILLIAM, A ;
WILLIS, AC ;
GORDON, S ;
MILON, G ;
KELM, S ;
BRADFIELD, P .
EMBO JOURNAL, 1994, 13 (19) :4490-4503
[5]   PROPERTIES AND DISTRIBUTION OF A LECTIN-LIKE HEMAGGLUTININ DIFFERENTIALLY EXPRESSED BY MURINE STROMAL TISSUE MACROPHAGES [J].
CROCKER, PR ;
GORDON, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (06) :1862-1875
[6]   Tuning antigen receptor signaling by CD22: Integrating cues from antigens and the microenvironment [J].
Cyster, JG ;
Goodnow, CC .
IMMUNITY, 1997, 6 (05) :509-517
[7]  
DORKEN B, 1986, J IMMUNOL, V136, P4470
[8]   Identification and molecular cloning of p75/AIRM1, a novel member of the sialoadhesin family that functions as an inhibitory receptor in human natural killer cells [J].
Falco, M ;
Biassoni, R ;
Bottino, C ;
Vitale, M ;
Sivori, S ;
Augugliaro, R ;
Moretta, L ;
Moretta, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (06) :793-801
[9]   CHARACTERIZATION OF CD33 AS A NEW MEMBER OF THE SIALOADHESIN FAMILY OF CELLULAR INTERACTION MOLECULES [J].
FREEMAN, SD ;
KELM, S ;
BARBER, EK ;
CROCKER, PR .
BLOOD, 1995, 85 (08) :2005-2012
[10]   Immunoreceptor tyrosine-based inhibition motif-bearing receptors regulate the immunoreceptor tyrosine-based activation motif-induced activation of immune competent cells [J].
Gergely, J ;
Pecht, I ;
Sármay, G .
IMMUNOLOGY LETTERS, 1999, 68 (01) :3-15