Published April 11, 2012 | Version v1
Journal article Open

Axin1 Prevents Salmonella Invasiveness and Inflammatory Response in Intestinal Epithelial Cells

  • 1. Rush University
  • 2. Rush University Medical Center
  • 3. University of Rochester
  • 4. Queen's University
  • 5. University of Chicago

Description

Background: Axin1 and its homolog Axin2 are scaffold proteins essential for regulating Wnt signaling. Axin-dependent regulation of Wnt is important for various developmental processes and human diseases. However, the involvement of Axin1 and Axin2 in host defense and inflammation remains to be determined.

Methods/Principal Findings: Here, we report that Axin1, but not Axin2, plays an essential role in host-pathogen interaction mediated by the Wnt pathway. Pathogenic Salmonella colonization greatly reduces the level of Axin1 in intestinal epithelial cells. This reduction is regulated at the posttranslational level in early onset of the bacterial infection. Further analysis reveals that the DIX domain and Ser614 of Axin1 are necessary for the Salmonella-mediated modulation through ubiquitination and SUMOylation.

Conclusion/Significance: Axin1 apparently has a preventive effect on bacterial invasiveness and inflammatory response during the early stages of infection. The results suggest a distinct biological function of Axin1 and Axin2 in infectious disease and intestinal inflammation while they are functionally equivalent in developmental settings.

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Additional details

Identifiers

DOI
10.1371/journal.pone.0034942
Other
oai:uchicago.tind.io:10769

Funding

National Institutes of Health
KO1 DK075386
National Institutes of Health
1R03DK089010-01
American Cancer Society
RSG-09-075-01-MBC
New York Stem Cell Foundation
Innovative, Developmental or Exploratory Activities award
National Institutes of Health
CA106308
National Institutes of Health
DE015654
Department of Defense
Idea Award

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Medicine, Pediatrics