Spontaneously developing chronic colitis in IL-10/iNOS double-deficient mice

• Published in: American journal of physiology: Gastrointestinal and liver physiology Vol. 279; no. 1; pp. G90 - G99
• Main Authors: McCafferty, D M, Sihota, E, Muscara, M, Wallace, J L, Sharkey, K A, Kubes, P
• Format: Journal Article
• Language: English
• Published: United States 01.07.2000
• Subjects: Age Factors; Animals; Blotting, Western; Chronic Disease; Colitis - enzymology; Colitis - genetics; Colitis - immunology; Colon - chemistry; Colon - enzymology; Colon - immunology; Female; Fluorescent Antibody Technique; Gene Expression Regulation, Enzymologic; Interleukin-10 - genetics; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Nitric Oxide Synthase - analysis; Nitric Oxide Synthase - genetics; Nitric Oxide Synthase Type II; Nitrites - blood; Peroxidase - metabolism; RNA, Messenger - analysis
• ISSN: 0193-1857; 1522-1547
• DOI: 10.1152/ajpgi.2000.279.1.g90

Mice deficient in both inducible nitric oxide synthase (iNOS) and interleukin (IL)-10 (iNOS(-/-)/IL-10(-/-)) were created to examine the role of iNOS in spontaneously developing intestinal inflammation. IL-10(-/-)/iNOS(-/-) mice were compared with IL-10(-/-) (iNOS(+/+)) littermates over 6 mo. RT-PCR, Western blot analysis, and immunohistochemistry were performed to measure iNOS message and protein levels. Plasma nitrate/nitrite (NO(x)) levels were assessed by HPLC. Damage scores (macroscopic and microscopic) and granulocyte infiltration were assessed. At 3-4 wk, IL-10(-/-) and IL-10(-/-)/iNOS(-/-) mice had no signs of colonic inflammation or granulocyte infiltration. Plasma NO(x) levels were not different from controls. By 3-4 mo, IL-10(-/-) mice had increased damage scores and granulocyte infiltration concurrent with increased mRNA and protein synthesis (restricted to the epithelium) for iNOS in intestinal tissues but not other tissues. Plasma NO(x) levels increased fivefold. Interestingly, in the absence of iNOS induction or increased plasma NO(x), iNOS(-/-)/IL-10(-/-) mice had damage and granulocyte infiltration equivalent to those observed in IL-10(-/-) littermates. These data suggest that iNOS does not impact on the development or severity of spontaneous chronic inflammation in IL-10-deficient mice.