Novel Subset of CD8α+ Dendritic Cells Localized in the Marginal Zone Is Responsible for Tolerance to Cell-Associated Antigens

被引:158
作者
Qiu, Chun-Hong [1 ]
Miyake, Yasunobu [1 ]
Kaise, Hitomi [1 ]
Kitamura, Hiroshi [2 ]
Ohara, Osamu [2 ,3 ]
Tanaka, Masato [1 ]
机构
[1] RIKEN Res Ctr Allergy & Immunol, Lab Innate Cellular Immun, Kanagawa 2300045, Japan
[2] RIKEN Res Ctr Allergy & Immunol, Lab Immunogenom, Kanagawa 2300045, Japan
[3] Kazusa DNA Res Inst, Dept Human Genome Res, Chiba, Japan
关键词
REGULATORY T-CELLS; APOPTOTIC CELLS; CROSS-PRESENTATION; IN-VIVO; IMMUNE TOLERANCE; DYING CELLS; RECEPTOR; PHOSPHATIDYLSERINE; ACTIVATION; MICE;
D O I
10.4049/jimmunol.0803364
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Apoptotic cell clearance by dendritic cells (DCs) plays a crucial role in the maintenance of self-tolerance. In spleen, CD8 alpha(+) DCs are thought to be responsible for this phenomenon by phagocytosing circulating apoptotic cells. However, as CD8 alpha(+) DCs are believed to be predominantly localized in the T cell zone, it remains unclear how these DCs phagocytose blood-borne apoptotic cells accumulated in the marginal zone (MZ). In this study, we identified a subpopulation of CD8 alpha(+) DCs responsible for tolerance induction to cell-associated Ags. Among splenic CD8 alpha(+) DCs, the CD103(+),CD207(+) subset was preferentially localized in the MZ and dominantly phagocytosed blood-borne apoptotic cells. After phagocytosis of apoptotic cells, this TIC subset migrated into the T cell zone for cross-presentation of cell-associated Ags. Stimulation of TLRs induced the disappearance of this DC subset. Consequently, CD8 alpha(+) DCs neither phagocytosed injected apoptotic cells nor presented cell-associated Ags in mice treated with TLR ligands. Transient ablation of this DC subset by cytochrome c injection resulted in a failure of tolerance induction to cell-associated Ags, indicating that this DC subset is essential for tolerance induction by apoptotic cell clearance. The Journal of Immunology, 2009, 182: 4127-4136.
引用
收藏
页码:4127 / 4136
页数:10
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