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Indole-3-carbinol prevents colitis and associated microbial dysbiosis in an IL-22–dependent manner
Philip B. Busbee, Lorenzo Menzel, Haider Rasheed Alrafas, Nicholas Dopkins, William Becker, Kathryn Miranda, Chaunbing Tang, Saurabh Chatterjee, Udai P. Singh, Mitzi Nagarkatti, Prakash S. Nagarkatti
Philip B. Busbee, Lorenzo Menzel, Haider Rasheed Alrafas, Nicholas Dopkins, William Becker, Kathryn Miranda, Chaunbing Tang, Saurabh Chatterjee, Udai P. Singh, Mitzi Nagarkatti, Prakash S. Nagarkatti
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Research Article Immunology Inflammation

Indole-3-carbinol prevents colitis and associated microbial dysbiosis in an IL-22–dependent manner

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Abstract

Colitis, an inflammatory bowel disease, is caused by a variety of factors, but luminal microbiota are thought to play crucial roles in disease development and progression. Indole is produced by gut microbiota and is believed to protect the colon from inflammatory damage. In the current study, we investigated whether indole-3-carbinol (I3C), a naturally occurring plant product found in numerous cruciferous vegetables, can prevent colitis-associated microbial dysbiosis and attempted to identify the mechanisms. Treatment with I3C led to repressed colonic inflammation and prevention of microbial dysbiosis caused by colitis, increasing a subset of gram-positive bacteria known to produce butyrate. I3C was shown to increase production of butyrate, and when mice with colitis were treated with butyrate, there was reduced colonic inflammation accompanied by suppression of Th17 and induction of Tregs, protection of the mucus layer, and upregulation in Pparg expression. Additionally, IL-22 was increased only after I3C but not butyrate administration, and neutralization of IL-22 prevented the beneficial effects of I3C against colitis, as well as blocked I3C-mediated dysbiosis and butyrate induction. This study suggests that I3C attenuates colitis primarily through induction of IL-22, which leads to modulation of gut microbiota that promote antiinflammatory butyrate.

Authors

Philip B. Busbee, Lorenzo Menzel, Haider Rasheed Alrafas, Nicholas Dopkins, William Becker, Kathryn Miranda, Chaunbing Tang, Saurabh Chatterjee, Udai P. Singh, Mitzi Nagarkatti, Prakash S. Nagarkatti

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Figure 5

Treatment with I3C or NaB prevents bacterial localization into the colonic crypts, maintains mucus production, and leads to upregulation in Pparg, but it only I3C increases IL-22 in the TNBS model.

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Treatment with I3C or NaB prevents bacterial localization into the colon...
(A) Colonic tissue sections were fixed and imaged with TEM. Representative images are shown for Vehicle (n = 6), I3C (n = 6), NaB (n = 6), TNBS + Vehicle (n = 6), TNBS + I3C (n = 6), and TNBS + NaB (n = 6). Black arrows indicate bacteria present in proximity to the colonic luminal surface microvilli, with TNBS + Vehicle image being a cross-section showing bacteria in the colonic crypt area. Scale bars indicated within images. (B) Colonic tissue sections were fixed and subjected to PAS staining. Representative images are shown for Vehicle (n = 6), I3C (n = 6), NaB (n = 6), TNBS + Vehicle (n = 6), TNBS + I3C (n = 6), and TNBS + NaB (n = 6). Scale bars: 100 μm (original magnification, ×100). Images are representative from 1 experiment out of 2 independent experiments performed. (C–E) Real-time PCR detecting colonic mRNA expression for Muc2 (C), Pparg (D), and IL-22 (E) was performed on colonic tissue samples (Vehicle n = 9, I3C n = 6, NaB n = 6, TNBS + Vehicle n = 9, TNBS + I3C n = 6, and TNBS + NaB n = 6) run in triplicate for each experimental group, and data are combined from 2 independent experiments. Data are shown as mean ± SEM, and significance was determined using 1-way ANOVA and Tukey’s multiple comparisons test; **P < 0.01; ***P < 0.005; ****P < 0.001.

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