Mindin is upregulated during colitis and may activate NF-kappaB in a TLR-9 mediated manner

World J Gastroenterol. 2010 Mar 7;16(9):1070-5. doi: 10.3748/wjg.v16.i9.1070.

Abstract

Aim: To investigate the regulation of mindin expression and the signaling pathway involved during inflammation.

Methods: C57BL/6 mice were treated with 3% dextran sulfate sodium (DSS) in drinking water for 6 d to induce acute colitis, and then the colon was harvested for histological analysis or for RNA isolation. mRNA expression of mindin and nuclear factor (NF)-kappaB p65 was analyzed by quantitative real time polymerase chain reaction (RT-PCR) and mindin expression construct was confirmed by Western blotting. Mouse macrophage and intestinal epithelial lineage cells were stimulated with different cytokines and toll-like receptor (TLR) ligands, before pNF-kappaB-luciferase activity was assessed using the Dual-Luciferase reporter assay system.

Results: mRNA expression of mindin was upregulated 4.7 + or - 1.1 fold compared with the baseline during DSS-induced intestinal inflammation in the mice. Stimulation with CpG-ODN (a known TLR-9 ligand) induced 4.2 + or - 0.3 fold upregulation of mindin expression in RAW 264.7 cells. Full-length of mindin was cloned from cDNA of mouse mesenteric lymph node, then the pCMV-Mindin-Flag expression vector was established and the protein expression level was confirmed. Transfection of the mindin construct and stimulation with CpG-ODN significantly increased the NF-kappaB-luciferase activity by 2.5 + or - 0.3 and 4.5 + or - 0.5 fold in RAW264.7 and CMT93 cells, respectively (P < 0.01).

Conclusion: Mindin expression is upregulated during intestinal inflammation and may induce NF-kappaB promoter activation in a TLR-9 mediated manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Blotting, Western
  • Cell Line
  • Cloning, Molecular
  • Colitis / chemically induced
  • Colitis / genetics
  • Colitis / immunology
  • Colitis / metabolism*
  • Colon / immunology
  • Colon / metabolism*
  • Dextran Sulfate
  • Disease Models, Animal
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism*
  • Genes, Reporter
  • Ligands
  • Macrophages / immunology
  • Mice
  • Mice, Inbred C57BL
  • Oligodeoxyribonucleotides / immunology
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic
  • RNA, Messenger / metabolism
  • Signal Transduction
  • Time Factors
  • Toll-Like Receptor 9 / metabolism*
  • Transcription Factor RelA / genetics
  • Transcription Factor RelA / metabolism*
  • Transfection
  • Up-Regulation

Substances

  • CPG-oligonucleotide
  • Extracellular Matrix Proteins
  • Ligands
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • Rela protein, mouse
  • Tlr9 protein, mouse
  • Toll-Like Receptor 9
  • Transcription Factor RelA
  • mindin
  • Dextran Sulfate