J Bacteriol Virol.  2005 Sep;35(3):217-226.

Nuclear Factor-kappa B Activation and Chemokine Genes Expression in HT-29 Intestinal Epithelial Cells in Response to Clostridium difficile Toxin A Stimulation

Affiliations
  • 1Department of Microbiology, Hanyang University College of Medicine, Korea. jungmogg@hanyang.ac.kr

Abstract

Intestinal epithelial cells are known to up-regulate the expression of several chemokines in response to bacterial toxins. Since there has been little understanding on the cellular mechanisms of C. difficile toxin A-induced mucosal inflammation, we investigated whether nuclear factor-kappa B (NF-kappaB) could regulate chemokine gene expression in HT-29 intestinal epithelial cells stimulated with C. difficile toxin A. C. difficile toxin A rapidly increased signals of NF-kappaB composed with p65 and p50 subunits in HT-29 cells, whereas it decreased the signals of IkappaBalpha. Blocking the NF-kB activation by transfection with dominant negative I kappa B alpha-containing retrovirus attenuated the upregulated expression of IL-8, GRO-alpha, and MCP-1 induced by C. difficile toxin A. These results suggest that NF-kappaB is a major regulator of chemokine gene expression in C. difficile toxin A-stimulated intestinal epithelial cells.

Keyword

C. difficile toxin A; Intestinal epithelial cells; NF-kappaB

MeSH Terms

Bacterial Toxins
Chemokines
Clostridium difficile*
Clostridium*
Epithelial Cells*
Gene Expression
HT29 Cells
Humans
I-kappa B Proteins
Inflammation
Interleukin-8
NF-kappa B
Retroviridae
Transfection
Bacterial Toxins
Chemokines
I-kappa B Proteins
Interleukin-8
NF-kappa B
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