C-type lectin DC-SIGN: An adhesion, signalling and antigen-uptake molecule that guides dendritic cells in immunity

被引:193
作者
Svajger, Urban [2 ]
Anderluh, Marko [3 ]
Jeras, Matjaz [2 ]
Obermajer, Natasa [1 ,4 ]
机构
[1] Jozef Stefan Inst, Dept Biotechnol, SI-1000 Ljubljana, Slovenia
[2] Blood Transfus Ctr Slovenia, Ljubljana 1000, Slovenia
[3] Fac Pharm, Dept Med Chem, SI-1000 Ljubljana, Slovenia
[4] Fac Pharm, Dept Pharmaceut Biol, SI-1000 Ljubljana, Slovenia
关键词
Dendritic cells; Pathogen recognition receptor; Adhesion; Migration; Endocytic receptor; Immune modulation; NF-KAPPA-B; RESPIRATORY SYNDROME CORONAVIRUS; HUMAN-IMMUNODEFICIENCY-VIRUS; MYCOBACTERIUM-TUBERCULOSIS; SELECTIVE RECOGNITION; HELICOBACTER-PYLORI; GENE-EXPRESSION; (ICAM-3)-GRABBING NONINTEGRIN; PATHOGEN RECOGNITION; CYTOKINE PRODUCTION;
D O I
10.1016/j.cellsig.2010.03.018
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN) is a type II C-type lectin whose expression is restricted to the most potent antigen-presenting cells (APCs), the dendritic cells (DCs). In recent years, DC-SIGN has gained an exponential increase in attention because of its involvement in multiple aspects of immune function. Besides being an adhesion molecule, particularly in binding ICAM-2 and ICAM-3, it is also crucial in recognizing several endogenous and exogenous antigens. Additionally, the intracellular domain of DC-SIGN includes molecular motifs, which enable the activation of signal transduction pathways involving Raf-1 and subsequent modulation of DC-maturation status, through direct modification of nuclear factor Nf-kappa B in DCs. Upon DC-SIGN engagement by mannose- or fucose-containing oligosaccharides, the latter leads to a tailored Toll-like receptor signalling, resulting in an altered DC-cytokine profile and skewing of Th1/Th2 responses. In this article, we will discuss recent advances on a broad perspective concerning DC-SIGN structure, signalling and immune function. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1397 / 1405
页数:9
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