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吲哚-3-甲醇通过依赖 IL-22 的方式预防结肠炎及其相关的微生物失调。

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

机构信息

Department of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, South Carolina, USA.

Department of Chemistry and Biochemistry, University of South Carolina College of Arts and Sciences, Columbia, South Carolina, USA.

出版信息

JCI Insight. 2020 Jan 16;5(1):127551. doi: 10.1172/jci.insight.127551.

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.

摘要

结肠炎,一种炎症性肠病,是由多种因素引起的,但腔微生物群被认为在疾病的发展和进展中起着至关重要的作用。吲哚是由肠道微生物群产生的,被认为可以保护结肠免受炎症损伤。在目前的研究中,我们调查了吲哚-3-甲醇(I3C),一种存在于许多十字花科蔬菜中的天然植物产物,是否可以预防结肠炎相关的微生物失调,并试图确定其机制。I3C 的治疗导致抑制结肠炎症和预防结肠炎引起的微生物失调,增加了一组已知产生丁酸盐的革兰氏阳性细菌。I3C 被证明可以增加丁酸盐的产生,当结肠炎小鼠用丁酸盐治疗时,结肠炎症减少,伴随着 Th17 的抑制和 Tregs 的诱导,粘液层的保护,以及 Pparg 表达的上调。此外,只有在给予 I3C 后才会增加 IL-22,而不是丁酸盐,中和 IL-22 可以防止 I3C 对结肠炎的有益作用,并阻止 I3C 介导的失调和丁酸盐诱导。这项研究表明,I3C 主要通过诱导 IL-22 来减轻结肠炎,从而调节肠道微生物群,促进抗炎性丁酸盐。

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