期刊
IMMUNITY
卷 38, 期 3, 页码 581-595出版社
CELL PRESS
DOI: 10.1016/j.immuni.2013.01.009
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资金
- Leona M. and Harry B. Helmsley Charitable Trust
- European Union [NMP4-LA-2009-229289]
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.
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