Gut dysbiosis from high-salt diet promotes glioma via propionate-mediated TGF-β activation.

IF 10.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-08-04 Epub Date: 2025-05-22 DOI:10.1084/jem.20241135
Chae Won Kim, Hyun-Jin Kim, In Kang, Keun Bon Ku, Yumin Kim, Jang Hyun Park, Juhee Lim, Byeong Hoon Kang, Won Hyung Park, Jeongwoo La, Sungwoo Chang, Inju Hwang, Minji Kim, Stephen Ahn, Heung Kyu Lee
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引用次数: 0

Abstract

The purpose of this study is to investigate the impact of a high-salt diet (HSD), which is commonly found in Western countries, on the progression of glioma. Our research shows that the alterations in gut microbiota caused by an HSD facilitated the development of glioma. Mice fed an HSD have elevated levels of intestinal propionate, which accelerated the growth of glioma cells. We also find that propionate supplementation enhanced the response of glioma cells to low oxygen levels. Moreover, we identify a link between TGF-β signaling, response to low oxygen levels, and invasion-related pathways. Propionate treatment increases the expression of HIF-1α, leading to an increase in TGF-β1 production. Additionally, propionate treatment promotes glioma cell invasion through TGF-β signaling. Our findings suggest that an HSD-induced increase in propionate plays a crucial role in glioma progression by facilitating invasion through the hypoxic response and TGF-β signaling pathways, thereby establishing a significant connection between gut microbiota and the progression of glioma.

高盐饮食引起的肠道生态失调通过丙酸介导的TGF-β激活促进胶质瘤。
本研究的目的是探讨西方国家普遍存在的高盐饮食(HSD)对胶质瘤进展的影响。我们的研究表明,由HSD引起的肠道微生物群的改变促进了胶质瘤的发展。喂食HSD的小鼠肠道丙酸水平升高,这加速了神经胶质瘤细胞的生长。我们还发现丙酸补充剂增强了胶质瘤细胞对低氧水平的反应。此外,我们确定了TGF-β信号,低氧水平反应和侵袭相关途径之间的联系。丙酸处理增加HIF-1α的表达,导致TGF-β1的产生增加。此外,丙酸治疗通过TGF-β信号传导促进胶质瘤细胞侵袭。我们的研究结果表明,hsd诱导的丙酸增加通过缺氧反应和TGF-β信号通路促进侵袭,在胶质瘤的进展中起着至关重要的作用,从而在肠道微生物群和胶质瘤的进展之间建立了重要的联系。
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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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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