Salt-responsive gut commensal modulates TH17 axis and disease

肠道微生物群 肠道菌群 自身免疫 肠-脑轴 实验性自身免疫性脑脊髓炎 免疫学 免疫系统 疾病 盐(化学) 生物 医学 微生物群 内科学 化学 生物信息学 物理化学
作者
Nicola Wilck,Mariana Matus,Sean M. Kearney,Scott W. Olesen,Sofia K. Forslund,Hendrik Bartolomaeus,Stefanie Haase,Anja Mähler,András Balogh,Lajos Markó,Olga Vvedenskaya,Friedrich H. Kleiner,D Tsvetkov,Lars Klug,Paul Igor Costea,Shinichi Sunagawa,Lisa Maier,Natalia Rakova,Valentin Schatz,Patrick Neubert
出处
期刊:Nature [Nature Portfolio]
卷期号:551 (7682): 585-589 被引量:1265
标识
DOI:10.1038/nature24628
摘要

A Western lifestyle with high salt consumption can lead to hypertension and cardiovascular disease. High salt may additionally drive autoimmunity by inducing T helper 17 (TH17) cells, which can also contribute to hypertension. Induction of TH17 cells depends on gut microbiota; however, the effect of salt on the gut microbiome is unknown. Here we show that high salt intake affects the gut microbiome in mice, particularly by depleting Lactobacillus murinus. Consequently, treatment of mice with L. murinus prevented salt-induced aggravation of actively induced experimental autoimmune encephalomyelitis and salt-sensitive hypertension by modulating TH17 cells. In line with these findings, a moderate high-salt challenge in a pilot study in humans reduced intestinal survival of Lactobacillus spp., increased TH17 cells and increased blood pressure. Our results connect high salt intake to the gut–immune axis and highlight the gut microbiome as a potential therapeutic target to counteract salt-sensitive conditions. High salt intake changed the gut microbiome and increased TH17 cell numbers in mice, and reduced intestinal survival of Lactobacillus species, increased the number of TH17 cells and increased blood pressure in humans. The role of the gut microbiota in human disease is becoming increasingly recognized. In this study, Dominik Müller and colleagues report that a diet high in salt alters the composition of the gut microbiota in mice, causing pronounced depletion of the commensal Lactobacillus murinus and reduced production of indole metabolites. Previous work has suggested that a high salt diet leads to the generation of pathogenic T helper 17 (TH17) cells, which have been linked to hypertension and autoimmunity. The authors show that treatment of mice on a high salt diet with L. murinus prevents salt-induced aggravation of actively induced autoimmune encephalomyelitis and salt-sensitive hypertension, through the suppression of TH17 cells. In a pilot study in a small number of humans, the authors also show that high-salt challenge induces an increase in blood pressure and TH17 cells, associated with a reduction in Lactobacillus in the gut. However, future work is required to determine whether the findings for mice are translatable to humans.
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