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Indole-3-carbinol prevents colitis and associated microbial dysbiosis in an IL-22–dependent manner
Philip B. Busbee, … , Mitzi Nagarkatti, Prakash S. Nagarkatti
Philip B. Busbee, … , Mitzi Nagarkatti, Prakash S. Nagarkatti
Published January 16, 2020
Citation Information: JCI Insight. 2020;5(1):e127551. https://doi.org/10.1172/jci.insight.127551.
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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 1

Treatment with I3C resulted in amelioration of TNBS-induced colitis.

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Treatment with I3C resulted in amelioration of TNBS-induced colitis.
(A)...
(A) TNBS colitis was induced in mice as described in Methods, and the efficacy of treatment with I3C was tested with the following experimental groups unless otherwise stated: Vehicle (n = 9), I3C (n = 5), TNBS + Vehicle (n = 9), TNBS + I3C (n = 9). (B–D) Disease parameters assessed included percent weight loss (B), colon length (C), and macroscopic score (D). (E) FITC-dextran was given to mice by oral gavage on day 3 of the TNBS model, and serum was collected 4 hours later to test gut permeability for Vehicle (n = 4), I3C (n = 4), TNBS + Vehicle (n = 4), and TNBS + I3C (n = 4), which are combined data from 2 independent experiments. (F) On day 3, serum was also collected to determine the levels of circulating SAA. (G and H) Bar plots depicting total cell numbers of Th17 (G) and Tregs (H) from MLN of experimental mice (n = 5). (I) Bar graph depicting colonoscopy scores from experimental mice (n = 5). (J) Bar graph depicting histopathological scores of H&E-stained colons from experimental mice (n = 5) (K) Representative colonoscopy images taken during day 3 of the TNBS model (n = 5). (L) Representative H&E stains of colons from experimental mice (n = 5). Scale bars: 100 μm (original magnification, ×100). Data are shown as mean ± SEM of combined data from at least 3 independent experiments unless otherwise stated. Significance was determined using 1-way ANOVA and Tukey’s multiple comparisons test; *P < 0.05; **P < 0.01; ***P < 0.005; ****P < 0.001.

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