4.8 Article

Generation of colonic IgA-secreting cells in the caecal patch

Journal

NATURE COMMUNICATIONS
Volume 5, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms4704

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology
  2. Japan Science and Technology Agency
  3. Ministry of Health, Labour and Welfare
  4. Osaka Foundation for Promotion of Clinical Immunology
  5. Grants-in-Aid for Scientific Research [24390120, 25893117, 25670272, 24111001, 24111005, 21229007, 23591632, 23501273] Funding Source: KAKEN

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Gut-associated lymphoid tissues are responsible for the generation of IgA-secreting cells. However, the function of the caecal patch, a lymphoid tissue in the appendix, remains unknown. Here we analyse the role of the caecal patch using germ-free mice colonized with intestinal bacteria after appendectomy. Appendectomized mice show delayed accumulation of IgA(+) cells in the large intestine, but not the small intestine, after colonization. Decreased colonic IgA(+) cells correlate with altered faecal microbiota composition. Experiments using photoconvertible Kaede-expressing mice or adoptive transfer show that the caecal patch IgA(+) cells migrate to the large and small intestines, whereas Peyer's patch cells are preferentially recruited to the small intestine. IgA(+) cells in the caecal patch express higher levels of CCR10. Dendritic cells in the caecal patch, but not Peyer's patches, induce CCR10 on cocultured B cells. Thus, the caecal patch is a major site for generation of IgA-secreting cells that migrate to the large intestine.

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