Maturation of the Mucosal Immune System Underlies Colitis Susceptibility in Interleukin-10-deficient (Il-10-/-) Mice.
From: Departments of Pathology, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4952, USA.
Journal of leukocyte biology
- Publish Date: Aug 2007
- ISSN: 0741-5400
- Volume: 82
- Issue: 2
- Pages: 311-9
- Medium: Print
- Language: English
- Citation (JAMA): Etling Michele R, Davies Sarah, Campbell Melanie, et al. Maturation of the Mucosal Immune System Underlies Colitis Susceptibility in Interleukin-10-deficient (Il-10-/-) Mice.. J. Leukoc. Biol. Aug 2007;82:311-9
Abstract
Elevated mucosal IL-12/23p40 and IFN-gamma accompany early inflammation in IL-10-deficient (IL-10(-/-)) mice and then later decline while inflammation persists. This report addresses whether this cytokine profile reflects disease progression or inherent, age-related changes in mucosal immunity. IL-10(-/-) and wild-type (WT) mice were maintained in an ultrabarrier facility or transferred to conventional housing at 3, 12, or 30 weeks of age. Weight, stool changes, and histologic features were followed. Lamina propria mononuclear cells were cultured for cytokine analysis by ELISA. Ultrabarrier-housed IL-10(-/-) mice are statistically indistinguishable from WT mice by weight, disease activity index, and histologic inflammation. IL-10(-/-) mice but not WT, transferred at 3 weeks, develop colitis gradually, reaching a significant, sustained maximum by 15 weeks of age. Transfer at 12 weeks induces rapid disease onset in both strains, maximal at 15 weeks of age. Inflammation persists in IL-10(-/-), and WT recover. IL-10(-/-) and WT mice transferred at 30 weeks demonstrate transient diarrhea and weight loss but no chronic inflammation. Probiotics delay symptom onset only in the 12-week-old group. IFN-gamma production from ultrabarrier-housed IL-10(-/-) mice is elevated at 12 weeks of age, and older animals have decreased IFN-gamma and increased IL-4. IL-10 is important for suppressing inflammation after transfer at 3 weeks of age and limiting inflammation after transfer at 12 weeks but has little influence at 30 weeks of age. Colitis onset, progression, and response to probiotic therapy vary with immune system age, suggesting that a distinct, Th1-driven, age-dependent cytokine profile may contribute to increased colitis susceptibility in otherwise healthy mice.
Mesh Headings (Keywords): Aging, Animals, Cells, Cultured, Colitis, Disease Susceptibility, Enzyme-Linked Immunosorbent Assay, Inflammation, Interferon Type II, Interleukin-10, Intestinal Mucosa, Mice, Mice, Inbred C57BL, Mice, Knockout, Monocytes, Mucous Membrane
Check for Full Text / PubMed Unique Identifier (PMID): 17456802
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