Microbial tryptophan metabolites modulate blood-brain and gut barriers in vitro

IF 3
Neuroscience Applied Pub Date : 2026-01-01 Epub Date: 2025-11-21 DOI:10.1016/j.nsa.2025.106876
Cristina Rosell-Cardona , Emily G. Knox , Paula Sánchez-Díaz , Sarah-Jane Leigh , Emanuela Tirelli , Michael S. Goodson , Nancy Kelley-Loughnane , María R. Aburto , Sarah Kittel-Schneider , John F. Cryan , Gerard Clarke
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Abstract

The gut microbiota influences brain function via the gut-brain axis, but the underlying molecular processes remain unclear. Critical to this communication are barrier systems, such as the epithelial gut and the blood-brain barrier, which mediate the interface between circulating signals and gut-brain communication. Microbial metabolites are key mediators of the gut microbiota that can influence barrier integrity. In this study, we used well-established in vitro models of the blood-brain and gut barriers and exposed them to a wide range of physiologically relevant stress-associated microbial metabolites, including tryptophan-derived metabolites with and without lipopolysaccharide (LPS) as a disrupting insult. We demonstrated that indole, indole-3-acetate, indole-3-propionate and tryptamine can modulate both gut and brain barriers in a dose- and cell-type dependent manner. Our findings suggest that specific indole metabolites should be further evaluated as promising novel therapeutic interventions to regulate barrier integrity along the microbiota-gut-brain axis.
微生物色氨酸代谢物在体外调节血脑和肠道屏障
肠道微生物群通过肠-脑轴影响大脑功能,但潜在的分子过程尚不清楚。这种沟通的关键是屏障系统,如肠上皮和血脑屏障,它们介导循环信号和肠-脑沟通之间的接口。微生物代谢物是影响屏障完整性的肠道微生物群的关键介质。在这项研究中,我们使用了成熟的体外血脑和肠道屏障模型,并将它们暴露于广泛的生理相关应激相关微生物代谢物中,包括色氨酸衍生代谢物,其中有或没有脂多糖(LPS)作为破坏性损伤。我们证明了吲哚、吲哚-3-醋酸酯、吲哚-3-丙酸酯和色胺可以以剂量和细胞类型依赖的方式调节肠道和脑屏障。我们的研究结果表明,特定的吲哚代谢物应该被进一步评估为有希望的新型治疗干预措施,以调节沿着微生物-肠道-脑轴的屏障完整性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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