TY - JOUR
T1 - Intestinal villous M cells
T2 - An antigen entry site in the mucosal epithelium
AU - Jang, Myoung Ho
AU - Kweon, Mi Na
AU - Iwatani, Koichi
AU - Yamamoto, Masafumi
AU - Terahara, Kazutaka
AU - Sasakawa, Chihiro
AU - Suzuki, Toshihiko
AU - Nochi, Tomonori
AU - Yokota, Yoshifumi
AU - Rennert, Paul D.
AU - Hiroi, Takachika
AU - Tamagawa, Hiroshi
AU - Iijima, Hideki
AU - Kunisawa, Jun
AU - Yuki, Yoshikazu
AU - Kiyono, Hiroshi
PY - 2004/4/20
Y1 - 2004/4/20
N2 - 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 β receptor (LTβR)-Ig-treated, lymphotoxin α (LTα)-/-, tumor necrosis factor/LTα-/-, 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.
AB - 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 β receptor (LTβR)-Ig-treated, lymphotoxin α (LTα)-/-, tumor necrosis factor/LTα-/-, 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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U2 - 10.1073/pnas.0400969101
DO - 10.1073/pnas.0400969101
M3 - Article
C2 - 15071180
AN - SCOPUS:11144358593
SN - 0027-8424
VL - 101
SP - 6110
EP - 6115
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 16
ER -