Diebold Sandra S
Peter Gorer Department of Immunobiology, King's College London, Guy's Hospital, London SE1 9RT, UK.
Handb Exp Pharmacol. 2009(188):3-30. doi: 10.1007/978-3-540-71029-5_1.
As sentinels of the immune system, dendritic cells (DC) scan their environment for the presence of pathogens. DC sense pathogens either directly or indirectly via endogenous factors such as cytokines and chemokines, which are produced by other cell types in response to infection. Although indirect signals in form of endogenous factors alert DC, direct activation of DC by pathogen-associated molecular patterns (PAMP) is crucial for the induction of primary T cell responses. Direct recognition of PAMP is mediated by pattern recognition receptors (PRR) such as Toll-like receptors (TLR) and C-type lectin receptors (CLR). The molecular patterns that are recognized by these receptors are indispensable for the life cycle of the pathogens, and their structure or cellular localization is different from that of the host. TLR detect cell-wall components of bacteria, fungi, and protozoa at the cell surface or bacterial and viral nucleic acid structures in a specialized endosomal compartment, while CLR that are involved in pattern recognition bind to carbohydrate structures associated with pathogens.
作为免疫系统的哨兵,树突状细胞(DC)在其周围环境中搜寻病原体的存在。DC通过细胞因子和趋化因子等内源性因子直接或间接感知病原体,这些内源性因子是其他细胞类型在感染时产生的。尽管内源性因子形式的间接信号会提醒DC,但病原体相关分子模式(PAMP)对DC的直接激活对于诱导初始T细胞反应至关重要。PAMP的直接识别由模式识别受体(PRR)介导,如Toll样受体(TLR)和C型凝集素受体(CLR)。这些受体识别的分子模式对于病原体的生命周期不可或缺,并且它们的结构或细胞定位与宿主不同。TLR在细胞表面检测细菌、真菌和原生动物的细胞壁成分,或在特殊的内体隔室中检测细菌和病毒核酸结构,而参与模式识别的CLR则与病原体相关的碳水化合物结构结合。