Two families of murine carbohydrate ligands for E-selectin

被引:22
作者
Osanai, T
Feizi, T
Chai, WG
Lawson, AM
Gustavsson, ML
Sudo, K
Araki, M
Araki, K
Yuen, CT
机构
[1] NORTHWICK PK HOSP & CLIN RES CTR,GLYCOSCI LAB,HARROW HA1 3UJ,MIDDX,ENGLAND
[2] UNIV TOKYO,INST MED SCI,TOKYO 108,JAPAN
[3] SAHLGRENS UNIV HOSP,GLYCO & TRANSPLANT BIOL DEPT CLIN CHEM & TRANSFUS,GOTHENBURG,SWEDEN
[4] UNIV GENEVA,DEPT PATHOL,GENEVA 4,SWITZERLAND
关键词
D O I
10.1006/bbrc.1996.0108
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
In search of endogenous oligosaccharide ligands for the endothelial adhesion molecule E-selectin in mouse, glycolipids from tissues and the neutrophilic cell line 32D c13 were tested for E-selectin binding. Kidneys of BALB/c and NMRI mice (but not CBA) and the 32D c13 cells were found to contain minor glycolipid populations that support strongly the binding of murine E-selectin. By chromatogram binding experiments and in situ liquid secondary ion mass spectrometry (LSIMS) with neoglycolipids derived from their endoglycoceramidase-released oligosaccharides, in conjunction with compositional and linkage analyses, one of the glycolipid ligands in kidney was identified as the Le(x)-active extended globo-glycolipid: Gal beta 1-4GlcNAc beta 1-6GalNAc beta 1-3Gal alpha 1-4Gal beta 1-4Glc beta 1-Cer Fuc alpha 1,3 Gal beta 1,3 Neoglycolipids enriched for the ligand structures were obtained from oligosaccharides released by endo-beta-galactosidase from the 32D c13 cells. By TLC-LSIMS and antibody binding, the main E-selectin binding determinant on these was identified as sialyl-Le(a). (C) 1996 Academic Press, Inc.
引用
收藏
页码:610 / 615
页数:6
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