Luminal Bacteria Recruit CD103+ Dendritic Cells into the Intestinal Epithelium to Sample Bacterial Antigens for Presentation

被引:380
作者
Farache, Julia [1 ]
Koren, Idan [1 ]
Milo, Idan [1 ]
Gurevich, Irina [1 ]
Kim, Ki-Wook [1 ]
Zigmond, Ehud [1 ]
Furtado, Glaucia C. [2 ]
Lira, Sergio A. [2 ]
Shakhar, Guy [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Mt Sinai Sch Med, Inst Immunol, New York, NY 10029 USA
关键词
IN-VIVO; LAMINA PROPRIA; T-CELLS; SALMONELLA-TYPHIMURIUM; TARGETED DISRUPTION; SEROVAR TYPHIMURIUM; LY6C(HI) MONOCYTES; IMMUNE-RESPONSES; DIFFERENTIATION; MOBILIZATION;
D O I
10.1016/j.immuni.2013.01.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
CD103(+) dendritic cells (DCs) carry bacteria from the small intestine and can present antigens to T cells. Yet they have not been recorded sampling luminal bacteria or presenting bacterial antigens in mesentery lymph nodes. We used 2-photon microscopy in live Cx3cr1(+/gfp) 3 Cd11c-YFP mice to study these processes. At steady state, sparse CD103(+) DCs occupied the epithelium. They patrolled among enterocytes while extending dendrites toward the lumen, likely using tight-junction proteins to penetrate the epithelium. Challenge with Salmonella triggered chemokine-and toll-like receptor (TLR)-dependent recruitment of additional DCs from the lamina propria (LP). The DCs efficiently phagocytosed the bacteria using intraepithelial dendrites. Noninvasive bacteria were similarly sampled. In contrast, CD103(+) DCs sampled soluble luminal antigen inefficiently. In mice harboring CD103(+) DCs, antigen-specific CD8 T cells were subsequently activated in MLNs. Intestinal CD103(+) DCs are therefore equipped with unique mechanisms to independently complete the processes of uptake, transportation, and presentation of bacterial antigens.
引用
收藏
页码:581 / 595
页数:15
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