Antigen Recognition and Presentation by Dendritic Cells

被引:0
作者
Kayo Inaba
Muneo Inaba
机构
[1] Graduate School of Biostudies,Laboratory of Immunobiology, Department of Animal Development and Physiology, Division of Systemic Life Science
[2] Kyoto University,First Department of Pathology
[3] Kansai Medical University,undefined
来源
International Journal of Hematology | 2005年 / 81卷
关键词
Dendritic cells; Antigen presentation; Cross-presentation; MHC molecules; Immunological synapse;
D O I
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中图分类号
学科分类号
摘要
In this article we review the following important points in the antigen-presenting system: (1) the regulation of the expression of major histocompatibility complex (MHC) molecules, (2) the mechanism of cross-presentation, and (3) the interaction of antigen-presenting cells (APC) and T-cells.The expression of MHC class I or class II molecules is regulated by the interaction of the MHC enhanceosome and the class II transactivator (CIITA). CIITA also regulates the gene expression of plexna-1, which encodes a semaphorin receptor, plexin-A1, that might be involved in the interaction with T-cells through an unknown ligand for plexin-A1.Two pathways, a proteasome/TAP-independent pathway and a proteasome/TAP-dependent pathway, have now been identified in the cross-presentation. In the proteasome/TAP-dependent pathway, the translocon/Sec61 protein channel is an important element for the transport of antigenic peptides in phagosomes to the cytoplasm.The integration of adhesion/costimulatory molecules and peptide-MHC complexes at the surface of APC creates the “immunological synapse” region, which potentiates the efficiency of APC-T-cell interactions. The peptide-MHC complexes preferentially reside in the “raft” structure or associate with tetraspanin family molecules.
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页码:181 / 187
页数:6
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