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

被引:366
作者
Jang, MH
Kweon, MN
Iwatani, K
Yamamoto, M
Terahara, K
Sasakawa, C
Suzuki, T
Nochi, T
Yokota, Y
Rennert, PD
Hiroi, T
Tamagawa, H
Iijima, H
Kunisawa, J
Yuki, Y
Kiyono, H
机构
[1] Osaka Univ, Res Inst Microbial Dis, Dept Mucosal Immunol, Suita, Osaka 5650871, Japan
[2] Int Vaccine Inst, Mucosal Immun Sect, Seoul 151818, South Korea
[3] Nihon Univ, Sch Dent, Dept Oral Med, Matsudo, Chiba 271, Japan
[4] Univ Tokyo, Inst Med Sci, Div Bacteriol, Tokyo 1088639, Japan
[5] JST, PRESTO, Kawaguchi, Saitama 3320012, Japan
[6] Fukui Med Univ, Dept Biochem 1, Matsuoka, Fukui 9101193, Japan
[7] Biogen Inc, Cambridge, MA 02142 USA
[8] JST, CREST, Kawaguchi, Saitama 3320012, Japan
[9] Univ Alabama, Immunobiol Vaccine Ctr, Birmingham, AL 35294 USA
[10] Univ Tokyo, Inst Med Sci, Div Mucosal Immunol, Tokyo 1088639, Japan
关键词
D O I
10.1073/pnas.0400969101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
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 a (LTalpha)(-/-), tumor necrosis factor/LTalpha(-/-), and inhibition of differentiation 2 (id2)(-/-) mice. Intestinal villous M cells have been observed to take up GFR-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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页码:6110 / 6115
页数:6
相关论文
共 48 条
[1]
Penetration of M cells and destruction of Peyer's patches by Yersinia enterocolitica: An ultrastructural and histological study [J].
Autenrieth, IB ;
Firsching, R .
JOURNAL OF MEDICAL MICROBIOLOGY, 1996, 44 (04) :285-294
[2]
EXPERIMENTAL YERSINIA-ENTEROCOLITICA INFECTION IN EUTHYMIC AND T-CELL-DEFICIENT ATHYMIC NUDE C57BL/6 MICE - COMPARISON OF TIME-COURSE, HISTOMORPHOLOGY, AND IMMUNE-RESPONSE [J].
AUTENRIETH, IB ;
VOGEL, U ;
PREGER, S ;
HEYMER, B ;
HEESEMANN, J .
INFECTION AND IMMUNITY, 1993, 61 (06) :2585-2595
[3]
BOLIN I, 1984, INFECT IMMUN, V43, P72
[4]
Borghesi C, 1999, LAB INVEST, V79, P1393
[5]
Borghesi C, 1996, J PATHOL, V180, P326, DOI 10.1002/(SICI)1096-9896(199611)180:3<326::AID-PATH656>3.0.CO
[6]
2-6
[7]
A model of host-microbial interactions in an open mammalian ecosystem [J].
Bry, L ;
Falk, PG ;
Midtvedt, T ;
Gordon, JI .
SCIENCE, 1996, 273 (5280) :1380-1383
[8]
USE OF THE NIRB PROMOTER TO DIRECT THE STABLE EXPRESSION OF HETEROLOGOUS ANTIGENS IN SALMONELLA ORAL VACCINE STRAINS - DEVELOPMENT OF A SINGLE-DOSE ORAL TETANUS VACCINE [J].
CHATFIELD, SN ;
CHARLES, IG ;
MAKOFF, AJ ;
OXER, MD ;
DOUGAN, G ;
PICKARD, D ;
SLATER, D ;
FAIRWEATHER, NF .
BIO-TECHNOLOGY, 1992, 10 (08) :888-892
[9]
M-cell surface β1 integrin expression and invasin-mediated targeting of Yersinia pseudotuberculosis to mouse Peyer's patch M cells [J].
Clark, MA ;
Hirst, BH ;
Jepson, MA .
INFECTION AND IMMUNITY, 1998, 66 (03) :1237-1243
[10]
Effect of mature lymphocytes and lymphotoxin on the development of the follicle-associated epithelium and M cells in mouse Peyer's patches [J].
Debard, N ;
Sierro, F ;
Browning, J ;
Kraehenbuhl, JP .
GASTROENTEROLOGY, 2001, 120 (05) :1173-1182