TY - JOUR
T1 - Luminal Bacteria Recruit CD103+ Dendritic Cells into the Intestinal Epithelium to Sample Bacterial Antigens for Presentation
AU - Farache, Julia
AU - Koren, Idan
AU - Milo, Idan
AU - Gurevich, Irina
AU - Kim, Ki Wook
AU - Zigmond, Ehud
AU - Furtado, Glaucia C.
AU - Lira, Sergio A.
AU - Shakhar, Guy
N1 - Funding Information:
We thank Oliver Pabst and Steffen Jung for critical discussion, Mary Jo Wick and Wolf-Dietrich Hardt for providing Salmonella strains, and Olga Schultz for technical advice. This work was supported by the Leona M. and Harry B. Helmsley Charitable Trust and by the “NanoII” grant (#NMP4-LA-2009-229289) from the European Union FP7 program.
PY - 2013/3/21
Y1 - 2013/3/21
N2 - 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 × 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.
AB - 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 × 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.
UR - http://www.scopus.com/inward/record.url?scp=84875489998&partnerID=8YFLogxK
U2 - 10.1016/j.immuni.2013.01.009
DO - 10.1016/j.immuni.2013.01.009
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C2 - 23395676
AN - SCOPUS:84875489998
SN - 1074-7613
VL - 38
SP - 581
EP - 595
JO - Immunity
JF - Immunity
IS - 3
ER -