Spontaneous and cytokine induced expression and activity of matrix metalloproteinases in human colonic epithelium

Clin Exp Immunol. 2009 Feb;155(2):257-65. doi: 10.1111/j.1365-2249.2008.03836.x.


Matrix metalloproteinases (MMPs) have been implicated in tissue damage associated with inflammatory bowel disease (IBD).As the role of the intestinal epithelium in this process is unknown, we determined MMP expression and enzyme activity in human colonic epithelial cells (CEC). MMP mRNA expression was assessed by reverse transcription-polymerase chain reaction in HT-29 and DLD-1 cells and in CEC isolated from biopsies from IBD and control patients. Total MMP activity in the cells was measured by a functional assay, based on degradation of a fluorescent synthetic peptide containing the specific bond for MMP cleavage. HT-29 and DLD-1 expressed several MMPs and levels of MMP-3, -10 and -13 mRNA expression were increased significantly by tumour necrosis factor (TNF)-alpha exposure. Transcripts of MMP-1, -3, -7, -9, -10 and -12 were detected in CECs and all, except MMP12, at significantly increased levels in cells from inflamed IBD mucosa. MMP-2 and -8 mRNA were expressed inconsistently and MMP-11, -13 and -14 mRNA undetectable. Proteolytic MMP activity was detected in CEC supernatants and the level was increased significantly in inflamed IBD epithelium. The enzyme activity was inhibited strongly by a specific MMP inhibitor (GM 6001). A significant TNF-alpha-mediated increase in MMP enzyme activity was also detected in HT-29 cells in vitro. In conclusion, the expression of several MMPs as well as the level of functional MMPactivity is increased in CEC from patients with active IBD. The results suggest that MMPs released by the intestinal epithelium may be involved in the pathogenesis of IBD by promoting local mucosal damage.

MeSH terms

  • Adult
  • Aged
  • Cell Line, Transformed
  • Cells, Cultured
  • Colon / drug effects
  • Colon / enzymology*
  • Cytokines / pharmacology*
  • Female
  • Gene Expression Regulation, Enzymologic / drug effects
  • Humans
  • Inflammatory Bowel Diseases / enzymology*
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / enzymology*
  • Male
  • Matrix Metalloproteinases / biosynthesis*
  • Matrix Metalloproteinases / genetics
  • Middle Aged
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Young Adult


  • Cytokines
  • RNA, Messenger
  • Matrix Metalloproteinases