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作 者:任建敏[1] 张彦洁[1] 王俊青[1] 吴菁[1] 刘昕訸[1] 杨芬[1] 许春娣[1] 周同[1]
机构地区:[1]上海交通大学医学院附属瑞金医院,上海200025
出 处:《生命科学》2012年第10期1075-1081,共7页Chinese Bulletin of Life Sciences
基 金:国家自然科学基金项目(81070567;8100-0163;81170383;81270801)
摘 要:DC-SIGN(DC-specific ICAM-3-grabbing non integrin,CD209)系C型凝集素家族主要成员,具有模式识别受体和介导细胞黏附功能。DC-SIGN可通过分子中凝集素糖识别域,识别多种病原体的外源性和机体内源性抗原以及细胞表面黏附分子(ICAM-2,3)中甘露糖或岩藻糖的糖基团,并对话协调Toll样受体等,介导树突状细胞(DC)等参与病原体或肿瘤细胞的免疫逃逸;也可调节DC黏附迁移并在炎症启动中激活初始T细胞免疫应答。因而,作为天然免疫分子介导基础,DC-SIGN在DC参与的感染性和炎症性疾病等的正负免疫调节中发挥了关键作用。目前有关DC-SIGN免疫调节效应涉及的信号转导以及分子表达调控机制尚未完全阐明,就相关进展作一综述。DC-SIGN (dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin) belongs to the major members of C-type lectin family, which is a PRR (pattern recognition receptor) and can mediate cell adhesion. DC-SIGN can specifically recognize glycoconjugates containing mannose or fucose in various exogenous antigen of pathogens, endogenous self-antigen and intercellular adhesion molecule 2,3 (ICAM-2, 3) by its lectin carbohydrate recognition domain. Moreover, it is also involved in immune escape of tumor cell or pathogens mediated by dendritic cells (DCs) through cross-talking with Toll like receptors. In the initial response of inflammation, DC-SIGN modulates the adhesion and migration of DCs to activate naive T-cell. Therefore, as an innate immune molecule, DC-SIGN plays an crucial role in infectious and inflammatory diseases through its positive and negative immunoregulatory effects on DCs. However, the immunoregulation mechanisms of DC-SIGN including signal transduction and expression regulation have not been fully elucidated. We have reviewed some progress in this field here.
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