期刊
INFLAMMATORY BOWEL DISEASES
卷 15, 期 6, 页码 890-899出版社
OXFORD UNIV PRESS INC
DOI: 10.1002/ibd.20850
关键词
colitis; interleukin-10; DSS; microarray; animal models; inflammation
资金
- National Institutes of Health (NIH) [R01 DK53347, P20 RR 020764-02, P40 RR 018603, P30 DK34987]
Background: While others have described gene expression patterns in humans with inflammatory bowel diseases and animals with chemically induced colitis, a genome-wide comparison of gene expression in genetically susceptible animals that develop spontaneous colitis has not been reported. Methods: We used microarray technology to compare gene expression profiles in cecal specimens from specific pathogen-free IL10-deficient (IL10-/-) mice with colitis and normal wildtype (WT) mice. RNA isolated from ceca of IL10-/- and WT mice was subjected to microarray analysis. The results were confirmed by real-time polymerase chain reaction (PCR) and immunofluorescence microscopy of selected Molecules. Expression of the selected genes in dextran sodium Sulfate (DSS)-treated mice with colitis and epithelial cell lines activated with pathophysiologic Stimuli was measured by real-time PCR. Results: Histological inflammation of the colon and IL-12/23p40 secretion from intestinal explants were greater in IL10-/- and DSS-treated mice versus WT and untreated mice. Microarray analysis demonstrated > 10-fold induction of the following molecules in the ceca of IL10-/- mice: mitochondrial ribosomal protein-L33, aquaporin-4, indoleamine-pyrrole-2,3-dioxygenase. and MHC class II with 63, 25, 20, and 12-fold increases, respectively. Cytochrome-P450, pancreatic lipase-related protein-2, and transthyretin were downregulated in IL10-/- mice. MHC II was increased throughout the colon, and aquaporin-4 was increased in the basolateral aspect of cecal epithelial cells. MHC 11 mRNA was increased in epithelial cells treated with IFN-gamma, but not TNF or Toll-like receptor ligands. Conclusions: Although most upregulated genes in experimental colitis are immune-related, aquaporin-4 and mitochondrial ribosomal protein-L33, which have not been previously associated with inflammation, were most highly upregulated.
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