Cryptosporidium parvum infection stimulates the secretion of TGF-beta, IL-8 and RANTES by Caco-2 cell line

Parasitol Res. 2000 Dec;86(12):947-9. doi: 10.1007/pl00008524.

Abstract

Cryptosporidium parvum is a common cause of diarrhea in humans. Although mild inflammatory mucosal infiltrate is usually observed, limited information is currently available on the pathogenic mechanisms involved in this phenomenon. The aim of this work was to investigate in vitro the influence of C. parvum infection on the secretion of lymphocyte-targeted chemokines (RANTES. MIP-1alpha, MIP-1beta, IL-8), proinflammatory cytokines (TNF-alpha, GM-CSF and IL-6) and TGF-beta by human enterocytic Caco-2 cells. C. parvum infection stimulates IL-8, RANTES and TGF-beta secretion by both the basal and apical side of caco-2 cells. A slight increase in TNF-alpha production by infected cells was observed in the apical compartment. Data suggest that enterocytic chemokines and/or TGF-beta are involved in the initiation and regulation of the mucosal response to C. parvum infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caco-2 Cells
  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokine CCL5 / metabolism*
  • Cryptosporidium parvum / immunology*
  • Cryptosporidium parvum / physiology
  • Enterocytes / immunology*
  • Enterocytes / parasitology*
  • Enzyme-Linked Immunosorbent Assay
  • Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Humans
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism*
  • Macrophage Inflammatory Proteins / metabolism
  • Transforming Growth Factor beta / metabolism*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokine CCL5
  • Interleukin-6
  • Interleukin-8
  • Macrophage Inflammatory Proteins
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Granulocyte-Macrophage Colony-Stimulating Factor