Citation

  • Authors: Choi, H. J., Kim, J., Park, S. H., Do, K. H., Yang, H., Moon, Y.
  • Year: 2012
  • Journal: Toxicol Lett 211 289-95
  • Applications: in vitro / DNA / jetPRIME
  • Cell type: HCT-8
    Description: Human ileocecal colorectal adenocarcinoma cells

Abstract

The widely used food additive carrageenan (CGN) has been shown to induce intestinal inflammation, ulcerative colitis-like symptoms, or neoplasm in the gut epithelia in animal models, which are also clinical features of human inflammatory bowel disease. In this study, the effects of CGN on pro-inflammatory transcription factors NF-kappaB and early growth response gene 1 product (EGR-1) were evaluated in terms of human intestinal epithelial barrier integrity. Both pro-inflammatory transcription factors were elevated by CGN and only NF-kappaB activation was shown to be involved in the induction of pro-inflammatory cytokine interleukin-8. Moreover, the integrity of the in vitro epithelial monolayer under the CGN insult was maintained by both activated pro-inflammatory transcription factors NF-kappaB and EGR-1. Suppression of NF-kappaB or EGR-1 aggravated barrier disruption by CGN, which was associated with the reduced gene expression of tight junction component zonula occludens 1 and its irregular localization in the epithelial monolayer.

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