DC-SIGN and SRCL bind glycans of carcinoembryonic antigen (CEA) and CEA-related cell adhesion molecule 1 (CEACAM1): recombinant human glycan-binding receptors as analytical tools

被引：13

作者：

Samsen, Alexandra ^{[1
]}

Bogoevska, Valentina ^{[1
]}

Klampe, Birgit ^{[1
]}

Bamberger, Ana-Maria ^{[3
]}

Lucka, Lothar ^{[2
]}

Horst, Andrea K. ^{[1
]}

Nollau, Peter ^{[1
]}

Wagener, Christoph ^{[1
]}

机构：

[1] Univ Med Ctr Hamburg Eppendorf, Inst Clin Chem, D-20251 Hamburg, Germany

[2] Inst Biochem & Mol Biol, D-14195 Berlin, Germany

[3] Univ Med Ctr Hamburg Eppendorf, Lab Endocrinol & Metab Ageing, D-20251 Hamburg, Germany

来源：

EUROPEAN JOURNAL OF CELL BIOLOGY | 2010年 / 89卷 / 01期

关键词：

CEA; CEACAM1; Lewis(x); High-mannose glycans; DC-SIGN; SRCL; Lectin; LEWIS-X RESIDUES; C-TYPE LECTIN; BILIARY GLYCOPROTEIN; DENDRITIC CELLS; HUMAN-TISSUES; HUMAN GRANULOCYTES; ESCHERICHIA-COLI; GENE FAMILY; IDENTIFICATION; EXPRESSION;

D O I：

10.1016/j.ejcb.2009.11.018

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Members of the family of carcinoembryonic antigen (CEA)-related cell adhesion molecules (CEACAMs) belonging to the immunoglobulin (Ig) superfamily are expressed in a variety of normal and malignant human tissues. As components of the cell membrane, these glycoproteins can make contact with adjacent cells. CEACAM1 and CEACAM5 (CEA) express Lewis(x) (Le(x)) structures. As shown by mass spectrometry in conjunction with enzymatic digestion, CEACAM1 contains at least seven Le(x) residues. Fucosyltransferase IX is the main fucosyltransferase responsible for attachment of terminal fucose, the key feature of the Le(x) structure, to CEA and CEACAM1. The Le(x) residues of both, CEACAM1 and CEA, interact with the human Le(x)-binding glycan receptors DC-SIGN and SRCL Since subpopulations of human macrophages express DC-SIGN or SRCL, Le(x)-carrying CEACAMs may modulate the immune response in normal tissues such as the human placenta or in malignant tumours, for example in colorectal, pancreatic or lung carcinomas. (C) 2009 Elsevier GmbH. All rights reserved.

引用

页码：87 / 94

页数：8

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