Lin Ming-Lee, Zhan Yifan, Villadangos Jose A, Lew Andrew M
The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Immunol Cell Biol. 2008 May-Jun;86(4):353-62. doi: 10.1038/icb.2008.3. Epub 2008 Feb 12.
The cell biology of cross-presentation is reviewed regarding exogenous antigen uptake, antigen degradation and entry into the major histocompatibility complex class I pathway. Whereas cross-presentation is not associated with enhanced phagocytic ability, certain receptors may favour uptake for cross-presentation for example mannose receptor for soluble glycoproteins. Perhaps, the defining property of the cross-presenting cell is some specialization in host machinery for handling and transport of antigen across organelles. Both cytosolic and vacuolar pathways are discussed. Which dendritic cell (DC) subset is the cross-presenting cell is explored. Cross-presentation is found within the CD8(+) subset resident in lymphoid organs. The role of other DC subsets (especially the migratory CD8(-) DC) and the route of antigen delivery are also discussed. Further consideration is given to antigen transfer between DC subsets and differential presentation to naive vs memory T cells.
本文综述了交叉呈递的细胞生物学,内容涉及外源性抗原摄取、抗原降解以及进入主要组织相容性复合体I类途径。虽然交叉呈递与吞噬能力增强无关,但某些受体可能有利于交叉呈递的摄取,例如可溶性糖蛋白的甘露糖受体。也许,交叉呈递细胞的决定性特性是宿主细胞内处理和跨细胞器转运抗原机制的某种特化。本文讨论了胞质途径和液泡途径。探讨了哪种树突状细胞(DC)亚群是交叉呈递细胞。在驻留在淋巴器官中的CD8(+)亚群内发现了交叉呈递。还讨论了其他DC亚群(特别是迁移性CD8(-) DC)的作用以及抗原递呈途径。进一步考虑了DC亚群之间的抗原转移以及对初始T细胞与记忆T细胞的差异呈递。