Published in:
01-11-2007 | Original Article
PPARβ/δ Protects Against Experimental Colitis Through a Ligand-Independent Mechanism
Authors:
Holly E. Hollingshead, Keiichirou Morimura, Masahiro Adachi, Mary J. Kennett, Andrew N. Billin, Timothy M. Willson, Frank J. Gonzalez, Jeffrey M. Peters
Published in:
Digestive Diseases and Sciences
|
Issue 11/2007
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Abstract
Peroxisome proliferator-activated receptors (PPARs) β/δ and γ have overlapping roles in the negative regulation of inflammatory response genes. Ligand activation of PPARγ protects against experimental colitis in mice. PPARβ/δ can negatively regulate inflammation and is highly expressed in the epithelial cells of the colon, therefore PPARβ/δ may also have a role in experimental colitis. In these studies, colitis was induced by dextran sodium sulfate (DSS) treatment in wild-type and PPARβ/δ-null mice, with and without the PPARβ/δ specific ligand GW0742. PPARβ/δ-null mice exhibited increased sensitivity to DSS-induced colitis, as shown by marked differences in body weight loss, colon length, colonic morphology, myeloperoxidase activity and increased expression of mRNAs encoding the inflammatory markers interferon γ, tumor necrosis factor-α, and interleukin-6 compared to similarly treated wild-type mice. Interestingly, these differences were not affected by ligand activation of PPARβ/δ in either genotype. These studies demonstrate that PPARβ/δ expression in the colonic epithelium inhibits inflammation and protects against DSS-induced colitis through a ligand-independent mechanism.