TY - JOUR
T1 - Distinct fucosylation of M cells and epithelial cells by Fut1 and Fut2, respectively, in response to intestinal environmental stress
AU - Terahara, Kazutaka
AU - Nochi, Tomonori
AU - Yoshida, Masato
AU - Takahashi, Yuko
AU - Goto, Yoshiyuki
AU - Hatai, Hirotsugu
AU - Kurokawa, Shiho
AU - Jang, Myoung Ho
AU - Kweon, Mi Na
AU - Domino, Steven E.
AU - Hiroi, Takachika
AU - Yuki, Yoshikazu
AU - Tsunetsugu-Yokota, Yasuko
AU - Kobayashi, Kazuo
AU - Kiyono, Hiroshi
N1 - Funding Information:
We thank Dr. Osamu Igarashi for technical support and Dr. Rebecca Devon for editing the manuscript. This work was supported in part by Grants from the Ministry of Education, Science, Sports and Culture of Japan (H.K. and K.T.), and the Ministry of Health, Labour and Welfare of Japan (H.K.).
PY - 2011/1/21
Y1 - 2011/1/21
N2 - The intestinal epithelium contains columnar epithelial cells (ECs) and M cells, and fucosylation of the apical surface of ECs and M cells is involved in distinguishing the two populations and in their response to commensal flora and environmental stress. Here, we show that fucosylated ECs (F-ECs) were induced in the mouse small intestine by the pro-inflammatory agents dextran sodium sulfate and indomethacin, in addition to an enteropathogen derived cholera toxin. Although F-ECs showed specificity for the M cell-markers, lectin Ulex europaeus agglutinin-1 and our monoclonal antibody NKM 16-2-4, these cells also retained EC-phenotypes including an affinity for the EC-marker lectin wheat germ agglutinin. Interestingly, fucosylation of Peyer's patch M cells and F-ECs was distinctly regulated by α(1,2)fucosyltransferase Fut1 and Fut2, respectively. These results indicate that Fut2-mediated F-ECs share M cell-related fucosylated molecules but maintain distinctive EC characteristics, Fut1 is, therefore, a reliable marker for M cells.
AB - The intestinal epithelium contains columnar epithelial cells (ECs) and M cells, and fucosylation of the apical surface of ECs and M cells is involved in distinguishing the two populations and in their response to commensal flora and environmental stress. Here, we show that fucosylated ECs (F-ECs) were induced in the mouse small intestine by the pro-inflammatory agents dextran sodium sulfate and indomethacin, in addition to an enteropathogen derived cholera toxin. Although F-ECs showed specificity for the M cell-markers, lectin Ulex europaeus agglutinin-1 and our monoclonal antibody NKM 16-2-4, these cells also retained EC-phenotypes including an affinity for the EC-marker lectin wheat germ agglutinin. Interestingly, fucosylation of Peyer's patch M cells and F-ECs was distinctly regulated by α(1,2)fucosyltransferase Fut1 and Fut2, respectively. These results indicate that Fut2-mediated F-ECs share M cell-related fucosylated molecules but maintain distinctive EC characteristics, Fut1 is, therefore, a reliable marker for M cells.
KW - Epithelial cell
KW - Fucosyltransferase
KW - Intestine
KW - M cell
KW - Peyer's patch
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U2 - 10.1016/j.bbrc.2010.12.067
DO - 10.1016/j.bbrc.2010.12.067
M3 - Article
C2 - 21172308
AN - SCOPUS:78751620999
SN - 0006-291X
VL - 404
SP - 822
EP - 828
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -