The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 Related articles in The JI
Right arrow Similar articles in this journal
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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Collier-Hyams, L. S.
Right arrow Articles by Neish, A. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Collier-Hyams, L. S.
Right arrow Articles by Neish, A. S.
The Journal of Immunology, 2005, 175: 4194-4198.
Copyright © 2005 by The American Association of Immunologists


CUTTING EDGE

Cutting Edge: Bacterial Modulation of Epithelial Signaling via Changes in Neddylation of Cullin-11

Lauren S. Collier-Hyams, Valerie Sloane, Brigid C. Batten and Andrew S. Neish2

Epithelial Pathobiology Unit, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta GA, 30322

The human enteric flora plays a significant role in intestinal health and disease. Certain enteric bacteria can inhibit the NF-{kappa}B pathway by blockade of I{kappa}B-{alpha} ubiquitination. I{kappa}B-{alpha} ubiquitination is catalyzed by the E3-SCF{beta}TrCP ubiquitin ligase, which is itself regulated via covalent modification of the cullin-1 subunit by the ubiquitin-like protein NEDD8. Neddylation is a biochemical event associated with diverse cellular processes related to cell signaling, however, physiological regulation of cullin neddylation has not been described in mammalian systems. We report that interaction of nonpathogenic bacteria with epithelial cells resulted in a rapid loss of neddylated Cul-1 and consequent repression of the NF-{kappa}B pathway. This observation may explain the ability of intestinal bacterial communities to influence diverse eukaryotic processes in general and inflammatory tolerance of the mammalian intestinal epithelia specifically.


Related articles in The JI:

IN THIS ISSUE

The JI 2005 175: 4159-4160. [Full Text]  



This article has been cited by other articles:


Home page
Physiol. GenomicsHome page
W. Rodenburg, I. M. J. Bovee-Oudenhoven, E. Kramer, R. van der Meer, and J. Keijer
Gene expression response of the rat small intestine following oral Salmonella infection
Physiol Genomics, July 18, 2007; 30(2): 123 - 133.
[Abstract] [Full Text] [PDF]


Home page
Nutr Clin PractHome page
J. Neu, M. Douglas-Escobar, and M. Lopez
Microbes and the Developing Gastrointestinal Tract
Nutr Clin Pract, April 1, 2007; 22(2): 174 - 182.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 2005 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 2005 by The American Association of Immunologists, Inc. All rights reserved.