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A novel therapy for colitis utilizing PPAR-γ ligands to inhibit the epithelial inflammatory response
Chinyu G. Su, … , Mitchell A. Lazar, Gary D. Wu
Chinyu G. Su, … , Mitchell A. Lazar, Gary D. Wu
Published August 15, 1999
Citation Information: J Clin Invest. 1999;104(4):383-389. https://doi.org/10.1172/JCI7145.
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Article

A novel therapy for colitis utilizing PPAR-γ ligands to inhibit the epithelial inflammatory response

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Abstract

Peroxisome proliferator-activated receptor γ (PPAR-γ), a member of the nuclear hormone receptor superfamily originally shown to play a critical role in adipocyte differentiation and glucose homeostasis, has recently been implicated as a regulator of cellular proliferation and inflammatory responses. Colonic epithelial cells, which express high levels of PPAR-γ protein, have the ability to produce inflammatory cytokines that may play a role in inflammatory bowel disease (IBD). We report here that PPAR-γ ligands dramatically attenuate cytokine gene expression in colon cancer cell lines by inhibiting the activation of nuclear factor-κB via an IκB-α–dependent mechanism. Moreover, thiazolidinedione ligands for PPAR-γ markedly reduce colonic inflammation in a mouse model of IBD. These results suggest that colonic PPAR-γ may be a therapeutic target in humans suffering from IBD.

Authors

Chinyu G. Su, Xiaoming Wen, Shannon T. Bailey, Wen Jiang, Shamina M. Rangwala, Sue A. Keilbaugh, Anne Flanigan, Sreekant Murthy, Mitchell A. Lazar, Gary D. Wu

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Figure 1

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PPAR-γ ligands inhibit cytokine gene expression in colon cancer cell lin...
PPAR-γ ligands inhibit cytokine gene expression in colon cancer cell lines. (a) The Caco-2 colon cancer cell line was treated with various concentrations of 15d-PGJ2 for 24 hours before immune stimulation with IL-1β for 90 minutes. (b) Quantitation of IL-8 mRNA expression in Caco-2 cells treated with various concentrations of 15d-PGJ2. Mean ± SD of 3 independent determinations. (c and d) HT-29 cells were treated for 24 hours with various concentrations of either 15d-PGJ2 (c) or BRL 49653 (d), followed by stimulation with IL-1β for 90 minutes.

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