Microbiota-derived I3A protects the intestine against radiation injury by activating AhR/IL-10/Wnt signaling and enhancing the abundance of probiotics.

IF 12.2 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Gut Microbes Pub Date : 2024-01-01 Epub Date: 2024-05-05 DOI:10.1080/19490976.2024.2347722
Li-Wei Xie, Shang Cai, Hai-Yan Lu, Feng-Ling Tang, Rui-Qiu Zhu, Ye Tian, Ming Li
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Abstract

The intestine is prone to radiation damage in patients undergoing radiotherapy for pelvic tumors. However, there are currently no effective drugs available for the prevention or treatment of radiation-induced enteropathy (RIE). In this study, we aimed at investigating the impact of indole-3-carboxaldehyde (I3A) derived from the intestinal microbiota on RIE. Intestinal organoids were isolated and cultivated for screening radioprotective tryptophan metabolites. A RIE model was established using 13 Gy whole-abdominal irradiation in male C57BL/6J mice. After oral administration of I3A, its radioprotective ability was assessed through the observation of survival rates, clinical scores, and pathological analysis. Intestinal stem cell survival and changes in the intestinal barrier were observed through immunofluorescence and immunohistochemistry. Subsequently, the radioprotective mechanisms of I3A was investigated through 16S rRNA and transcriptome sequencing, respectively. Finally, human colon cancer cells and organoids were cultured to assess the influence of I3A on tumor radiotherapy. I3A exhibited the most potent radioprotective effect on intestinal organoids. Oral administration of I3A treatment significantly increased the survival rate in irradiated mice, improved clinical and histological scores, mitigated mucosal damage, enhanced the proliferation and differentiation of Lgr5+ intestinal stem cells, and maintained intestinal barrier integrity. Furthermore, I3A enhanced the abundance of probiotics, and activated the AhR/IL-10/Wnt signaling pathway to promote intestinal epithelial proliferation. As a crucial tryptophan metabolite, I3A promotes intestinal epithelial cell proliferation through the AhR/IL-10/Wnt signaling pathway and upregulates the abundance of probiotics to treat RIE. Microbiota-derived I3A demonstrates potential clinical application value for the treatment of RIE.

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微生物群衍生的 I3A 可通过激活 AhR/IL-10/Wnt 信号和提高益生菌的丰度来保护肠道免受辐射损伤。
接受盆腔肿瘤放射治疗的患者的肠道很容易受到辐射损伤。然而,目前还没有有效的药物可用于预防或治疗辐射诱发的肠病(RIE)。在这项研究中,我们旨在研究从肠道微生物群中提取的吲哚-3-甲醛(I3A)对 RIE 的影响。为了筛选具有辐射防护作用的色氨酸代谢物,我们分离并培养了肠道有机体。通过对雄性 C57BL/6J 小鼠进行 13 Gy 全腹照射,建立了 RIE 模型。口服 I3A 后,通过观察存活率、临床评分和病理分析评估其辐射防护能力。通过免疫荧光和免疫组化观察了肠干细胞的存活率和肠屏障的变化。随后,分别通过 16S rRNA 和转录组测序研究了 I3A 的放射保护机制。最后,通过培养人结肠癌细胞和器官组织来评估 I3A 对肿瘤放疗的影响。结果表明,I3A对肠道有机体具有最强的放射保护作用。口服 I3A 能显著提高辐照小鼠的存活率,改善临床和组织学评分,减轻粘膜损伤,促进 Lgr5+ 肠干细胞的增殖和分化,维持肠屏障的完整性。此外,I3A 还能提高益生菌的丰度,激活 AhR/IL-10/Wnt 信号通路,促进肠上皮细胞增殖。作为一种重要的色氨酸代谢物,I3A通过AhR/IL-10/Wnt信号通路促进肠上皮细胞增殖,并上调益生菌的丰度,从而治疗RIE。微生物群衍生的I3A在治疗RIE方面具有潜在的临床应用价值。
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来源期刊
Gut Microbes
Gut Microbes Medicine-Microbiology (medical)
CiteScore
18.20
自引率
3.30%
发文量
196
审稿时长
10 weeks
期刊介绍: The intestinal microbiota plays a crucial role in human physiology, influencing various aspects of health and disease such as nutrition, obesity, brain function, allergic responses, immunity, inflammatory bowel disease, irritable bowel syndrome, cancer development, cardiac disease, liver disease, and more. Gut Microbes serves as a platform for showcasing and discussing state-of-the-art research related to the microorganisms present in the intestine. The journal emphasizes mechanistic and cause-and-effect studies. Additionally, it has a counterpart, Gut Microbes Reports, which places a greater focus on emerging topics and comparative and incremental studies.
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