Identification, characterization and leucocyte expression of Siglec-10, a novel human sialic acid-binding receptor

被引:105
作者
Munday, J
Kerr, S
Ni, J
Cornish, AL
Zhang, JQ
Nicoll, G
Floyd, H
Mattei, MG
Moore, P
Liu, D
Crocker, PR [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Wellcome Trust Bioctr, Dundee DD1 5EH, Scotland
[2] Human Genome Sci Inc, Rockville, MD 20850 USA
[3] Fac Med Marseille, Unite Genet Med & Dev, INSERM U491, F-13385 Marseille 5, France
关键词
immunoglobulin superfamily; inhibitory receptor; innate immunity; lectin;
D O I
10.1042/0264-6021:3550489
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
Here we characterize Siglec-10 as a new member of the Siglec family of sialic acid-binding Ig-like lectins, A full-length cDNA was isolated from a human spleen library and the corresponding gene identified. Siglec-10 is predicted to contain five extracellular Ig-like domains and a cytoplasmic tail containing three putative tyrosine-based signalling motifs. Siglec-10 exhibited a high degree of sequence similarity to CD33-related Siglecs and mapped to the same region, on chromosome 19q13,3. The expressed protein was able to mediate sialic acid-dependent binding to human erythrocytes and soluble sialoglycoconjugates. Using specific antibodies, Siglec-10 was detected on subsets of human leucocytes including eosinophils, monocytes and a minor population of natural killer-like cells. The molecular properties and expression pattern suggest that Siglec-10 may function as an inhibitory receptor within the innate immune system.
引用
收藏
页码:489 / 497
页数:9
相关论文
共 47 条
[1]   Cloning, characterization, and phylogenetic analysis of Siglec-9, a new member of the CD33-related group of Siglecs - evidence for co-evolution with sialic acid synthesis pathways [J].
Angata, T ;
Varki, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (29) :22127-22135
[2]   Siglec-7: a sialic acid-binding lectin of the immunoglobulin superfamily [J].
Angata, T ;
Varki, A .
GLYCOBIOLOGY, 2000, 10 (04) :431-438
[3]  
BRAESCHANDERSEN S, 1994, J BIOL CHEM, V269, P11783
[4]   EPIDERMAL GROWTH-FACTOR REGULATES P21(RAS) THROUGH THE FORMATION OF A COMPLEX OF RECEPTOR, GRB2 ADAPTER PROTEIN, AND SOS NUCLEOTIDE EXCHANGE FACTOR [J].
BUDAY, L ;
DOWNWARD, J .
CELL, 1993, 73 (03) :611-620
[5]   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
[6]   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
[7]  
CROCKER RP, 1998, GLYCOBIOLOGY, V8, pR5
[8]   Tuning antigen receptor signaling by CD22: Integrating cues from antigens and the microenvironment [J].
Cyster, JG ;
Goodnow, CC .
IMMUNITY, 1997, 6 (05) :509-517
[9]   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
[10]  
FELSENSTEIN J, 1985, EVOLUTION, V39, P783, DOI 10.1111/j.1558-5646.1985.tb00420.x