Intestinal villous M cells: An antigen entry site in the mucosal epithelium

Myoung Ho Jang(Nihon University), Mi–Na Kweon(Nihon University), Koichi Iwatani(Nihon University), Masafumi Yamamoto(Nihon University), Kazutaka Terahara(Nihon University), Chihiro Sasakawa(Nihon University), Toshihiko Suzuki(Nihon University), Tomonori Nochi(Nihon University), Yoshifumi Yokota(Nihon University), Paul D. Rennert(Nihon University), Takachika Hiroi(Nihon University), Hiroshi Tamagawa(Nihon University), Hideki Iijima(Nihon University), Jun Kunisawa(Nihon University), Yoshikazu Yuki(Nihon University), Hiroshi Kiyono(Nihon University)
Proceedings of the National Academy of Sciences
April 7, 2004
Cited by 458Open Access
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Abstract

M cells located in the follicle-associated epithelium of Peyer's patches (PP) are shown to be the principal sites for the sampling of gut luminal antigens. Thus, PP have long been considered the gatekeepers of the mucosal immune system. Here, we report a distinct gateway for the uptake of gut bacteria: clusters of non-follicle-associated epithelium-associated Ulex europaeus agglutinin (UEA)-1(+) cells, which we have designated intestinal villous M cells. Interestingly, villous M cells are developed in various PP [or gut-associated lymphoid tissue (GALT)]-null mice, such as in utero lymphotoxin beta receptor (LTbetaR)-Ig-treated, lymphotoxin alpha (LTalpha)(-/-), tumor necrosis factor/LTalpha(-/-), and inhibition of differentiation 2 (Id2)(-/-) mice. Intestinal villous M cells have been observed to take up GFP-expressing Salmonella, Yersinia, and Escherichia coli-expressing invasin, as well as gut bacterial antigen for subsequent induction of antigen-specific immune responses. Thus, the identified villous M cells could be an alternative and PP-independent gateway for the induction of antigen-specific immune responses by means of the mucosal compartment.


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