Selective Role of TNFα and IL10 in Regulation of Barrier Properties of the Colon in DMH-Induced Tumor and Healthy Rats

Int J Mol Sci. 2022 Dec 9;23(24):15610. doi: 10.3390/ijms232415610.

Abstract

Recently it has been reported that the tumor adjacent colon tissues of 1,2-dymethylhydrazine induced (DMH)-rats revealed a high paracellular permeability. We hypothesized that the changes might be induced by cytokines. Colorectal cancer is accompanied by an increase in tumor necrosis factor alpha (TNFα) and interleukin 10 (IL10) that exert opposite regulatory effects on barrier properties of the colon, which is characterized by morphological and functional segmental heterogeneity. The aim of this study was to analyze the level of TNFα and IL10 in the colon segments of DMH-rats and to investigate their effects on barrier properties of the proximal and distal parts of the colon in healthy rats. Enzyme immunoassay analysis showed decreased TNFα in tumors in the distal part of the colon and increased IL10 in proximal tumors and in non-tumor tissues. Four-hour intraluminal exposure of the colon of healthy rats with cytokines showed reduced colon barrier function dependent on the cytokine: TNFα decreased it mainly in the distal part of the colon, whereas IL10 decreased it only in the proximal part. Western blot analysis revealed a more pronounced influence of IL10 on tight junction (TJ) proteins expression by down-regulation of the TJ proteins claudin-1, -2 and -4, and up-regulation of occludin only in the proximal part of the colon. These data may indicate a selective role of the cytokines in regulation of the barrier properties of the colon and a prominent role of IL10 in carcinogenesis in its proximal part.

Keywords: 1,2-dimethylhydrazine; barrier properties; colon; colorectal cancer; cytokines; heterogeneity; interleukin 10; rat; tight junction proteins; tumor necrosis factor alpha.

MeSH terms

  • Animals
  • Colon / metabolism
  • Colonic Neoplasms* / chemically induced
  • Colonic Neoplasms* / metabolism
  • Cytokines / metabolism
  • Interleukin-10* / metabolism
  • Rats
  • Tight Junction Proteins / metabolism
  • Tight Junctions / metabolism
  • Tumor Necrosis Factor-alpha* / metabolism

Substances

  • Cytokines
  • Interleukin-10
  • Tight Junction Proteins
  • Tumor Necrosis Factor-alpha