AJP - GI Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Gastrointest Liver Physiol 293: G780-G787, 2007. First published August 2, 2007; doi:10.1152/ajpgi.00010.2007
0193-1857/07 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
293/4/G780    most recent
00010.2007v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Meng, D.
Right arrow Articles by Nanthakumar, N. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Meng, D.
Right arrow Articles by Nanthakumar, N. N.

MUCOSAL BIOLOGY

Bacterial symbionts induce a FUT2-dependent fucosylated niche on colonic epithelium via ERK and JNK signaling

Di Meng,1 David S. Newburg,1 Cheryl Young,1 Amy Baker,1 Susan L. Tonkonogy,2 R. Balfour Sartor,3 W. Allan Walker,1 and N. Nanda Nanthakumar1

1Developmental Gastroenterology Laboratory, Pediatric Gastroenterology and Nutrition Unit, Department of Pediatrics, Massachusetts General Hospital for Children and Harvard Clinical Nutrition Research Center, Harvard Medical School, Boston, Massachusetts; 2Department of Microbiology, Pathology and Parasitology, North Carolina State University College of Veterinary Medicine, Raleigh, North Carolina; and 3Center for Gastrointestinal Biology and Disease, Division of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, North Carolina

Submitted 5 January 2007 ; accepted in final form 29 July 2007

The intestinal epithelium of the adult gut supports a complex, dynamic microbial ecosystem and expresses highly fucosylated glycans on its surface. Uncolonized gut contains little fucosylated glycan. The transition toward adult colonization, such as during recovery from germ-free status or from antibiotic treatment, increased expression of fucosylated epitopes in the colonic epithelium. This increase in fucosylation is accompanied by induction of fut2 mRNA expression and {alpha}1,2/3-fucosyltransferase activity. Colonization stimulates ERK and JNK signal transduction pathways, resulting in activation of transcription factors ATF2 and c-Jun, respectively. This increases transcription of fut2 mRNA and expression of {alpha}1,2/3-fucosyltransferase activity, resulting in a highly fucosylated intestinal mucosa characteristic of the adult mammalian gut. Blocking the ERK and JNK signaling cascade inhibits the ability of colonization to induce elevated fut2 mRNA and fucosyltransferase activity in the mature colon. Thus pioneer-mutualist symbiotic bacteria may utilize the ERK and JNK signaling cascade to induce the high degree of fucosylation characteristic of adult mammalian colon, and we speculate that this fucosylation facilitates colonization by adult microbiota.

bacterial colonization; fucosylation



Address for reprint requests and other correspondence: N. Nanthakumar, Developmental Gastroenterology Laboratory, Massachusetts General Hospital-East, 114 16th St., Rm 3650, Charlestown, MA 02129 (e-mail: nanthaku{at}helix.mgh.harvard.edu)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.