Ackerman Anne L, Cresswell Peter
Section of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, P.O. Box 208011, New Haven, Connecticut 06520-8011, USA.
Nat Immunol. 2004 Jul;5(7):678-84. doi: 10.1038/ni1082.
The recent discovery of fusion of endoplasmic reticulum membrane with nascent phagosomes suggests that this peripheral compartment in macrophages and dendritic cells may serve as an organelle optimized for major histocompatibility complex (MHC) class I-restricted cross-presentation of exogenous antigens. The process allows intersection of the endosomal system with the endoplasmic reticulum, the classical site of MHC class I peptide loading, and may reconcile the seemingly conflicting evidence indicating both of these sites are crucial in cross-presentation. Here we discuss the potential mechanisms involved in loading exogenous antigens onto MHC class I molecules and the implications of this new evidence for the in vivo function of dendritic cells.
内质网膜与新生吞噬体融合的最新发现表明,巨噬细胞和树突状细胞中的这个外周区室可能作为一种细胞器,专为主要组织相容性复合体(MHC)I类限制的外源性抗原交叉呈递而优化。该过程使内体系统与内质网(MHC I类肽加载的经典位点)相交,并且可能调和表明这两个位点在交叉呈递中都至关重要的看似相互矛盾的证据。在这里,我们讨论了将外源性抗原加载到MHC I类分子上所涉及的潜在机制,以及这一新证据对树突状细胞体内功能的影响。