Intracellular Assembly and Trafficking of MHC Class I Molecules

被引:76
作者
Donaldson, Julie G. [1 ]
Williams, David B. [2 ,3 ]
机构
[1] NHLBI, Cell Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院;
关键词
antigen presentation; endocytosis; endoplasmic reticulum; membrane traffic; molecular chaperones; peptide loading complex; ubiquitylation; COMPLEX CLASS-I; CLATHRIN-INDEPENDENT ENDOCYTOSIS; PEPTIDE-LOADING COMPLEX; NEGATIVE CELL-LINE; ENDOPLASMIC-RETICULUM; HISTOCOMPATIBILITY MOLECULES; RECYCLING PATHWAY; DOWN-REGULATION; QUALITY-CONTROL; ANTIGEN PRESENTATION;
D O I
10.1111/j.1600-0854.2009.00979.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The presentation of antigenic peptides by class I molecules of the major histocompatibility complex begins in the endoplasmic reticulum (ER) where the co-ordinated action of molecular chaperones, folding enzymes and class I-specific factors ensures that class I molecules are loaded with high-affinity peptide ligands that will survive prolonged display at the cell surface. Once assembled, class I molecules are released from the quality-control machinery of the ER for export to the plasma membrane where they undergo dynamic endocytic cycling and turnover. We review recent progress in our understanding of class I assembly, anterograde transport and endocytosis and highlight some of the events targeted by viruses as a means to evade detection by cytotoxic T cells and natural killer cells.
引用
收藏
页码:1745 / 1752
页数:8
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