Norbury C C, Hewlett L J, Prescott A R, Shastri N, Watts C
Department of Biochemistry, University of Dundee, Scotland.
Immunity. 1995 Dec;3(6):783-91. doi: 10.1016/1074-7613(95)90067-5.
Extracellular proteins are not generally presented on class I MHC molecules in vitro, yet many studies show that a pathway exists in vivo for the presentation of extracellular material on class I molecules to prime CD8+ T cell responses. Here, we provide morphological evidence that proteins taken up by macropinocytosis can gain access to the cytosol and therefore into the conventional class I MHC pathway. Class I presentation of soluble ovalbumin by mouse bone marrow macrophages was dramatically enhanced by MCSF or phorbol ester and blocked by amiloride, which stimulate and inhibit membrane ruffling and macropinocytosis, respectively. Brefeldin A, gelonin, and a peptide aldehyde inhibitor of proteasomal processing each blocked presentation of macropinocytosed antigen, demonstrating that unusual access to the conventional class I MHC pathway was occurring. This novel cell type-specific endocytic pathway may facilitate presentation of exogenous material on class I MHC molecules, allowing induction of CD8+ T cell responses to soluble proteins, tumor cell fragments, and some pathogens.
细胞外蛋白质在体外一般不会呈递于I类主要组织相容性复合体(MHC)分子上,但许多研究表明,体内存在一条将细胞外物质呈递于I类分子上以启动CD8 + T细胞应答的途径。在此,我们提供形态学证据表明,通过巨吞饮作用摄取的蛋白质能够进入细胞质溶胶,进而进入传统的I类MHC途径。小鼠骨髓巨噬细胞对可溶性卵清蛋白的I类呈递被巨噬细胞集落刺激因子(MCSF)或佛波酯显著增强,并被分别刺激和抑制膜皱褶和巨吞饮作用的阿米洛利所阻断。布雷菲德菌素A、凝胶onin和蛋白酶体加工的肽醛抑制剂均阻断了巨吞饮抗原的呈递,表明正在发生对传统I类MHC途径的异常进入。这种新型的细胞类型特异性内吞途径可能有助于将外源性物质呈递于I类MHC分子上,从而诱导对可溶性蛋白质、肿瘤细胞片段和某些病原体的CD8 + T细胞应答。