Bryant Paula, Ploegh Hidde
Department of Microbiology, The Ohio State University, 484 West 12th Avenue, Columbus, OH 43210, USA.
Curr Opin Immunol. 2004 Feb;16(1):96-102. doi: 10.1016/j.coi.2003.11.011.
The loading of class II MHC molecules with antigenic peptides is largely confined to the endocytic vesicles of specialized antigen-presenting cells (APCs), such as B cells, macrophages and dendritic cells. At first glance, the pathway utilized by each of these professional APCs to generate class II-peptide complexes on their surface appears to be indistinguishable. All three types of APC rely on the chaperone Ii for correct class II assembly and transport to the endocytic pathway, they all depend on the action of specific cysteine proteases to remove Ii from the class II-Ii complex, and they all utilize the class II-like molecule DM to facilitate peptide loading. A closer look, however, reveals subtle yet important differences in the class II maturation pathway between each of these APCs, which befit the unique roles these individual cells play in eliciting CD4(+) T-cell responses.
II类主要组织相容性复合体(MHC)分子与抗原肽的装载主要局限于特殊抗原呈递细胞(APC)的内吞囊泡,如B细胞、巨噬细胞和树突状细胞。乍一看,这些专职APC中的每一种在其表面生成II类肽复合物所利用的途径似乎难以区分。所有这三种类型的APC都依赖伴侣蛋白Ii来进行正确的II类组装并转运至内吞途径,它们都依赖特定半胱氨酸蛋白酶的作用从II类-Ii复合物中去除Ii,并且它们都利用II类样分子DM来促进肽的装载。然而,仔细观察会发现这些APC中每一种在II类成熟途径上存在细微但重要的差异,这与这些单个细胞在引发CD4(+) T细胞应答中所起的独特作用相符。