Phocaeicola dorei and Phocaeicola vulgatus Protect against Atherosclerosis by Regulating Gut Immunity.

IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE
Hitomi Nakashima, Ryohei Shinohara, Takuo Emoto, Yoshihiro Saito, Naofumi Yoshida, Ken-Ichi Hirata, Takumi Murakami, Hiroshi Mori, Atsushi Toyoda, Tomomi Sugiyama, Takuji Yamada, Tomoya Yamashita
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Abstract

Aim: Arteriosclerosis is a condition that leads to coronary artery disease (CAD) and stroke. Basic and clinical studies have suggested a link between the gut microbiota and various diseases, including atherosclerosis. Therefore, we focused on gut microbiota and aimed to develop a probiotic-based treatment for atherosclerosis.

Method: From 6 to 14 weeks of age, apoE-deficient mice, a mouse model of atherosclerosis, were orally administered with Phocaeicola dorei and Phocaeicola vulgatus or saline five times/week. The diet was changed to a western diet at eight weeks of age. Finally, the mice were sacrificed at 14 weeks of age, and the atherosclerotic lesion area was evaluated.

Result: Previous studies have shown that atherosclerosis is suppressed by the administration of live type strains (TS) of P. dorei and P. vulgatus in apoE-deficient mice. In this study, we isolated P. vulgatus AF299, which highly expresses commensal colonization factors. Oral administration of P. dorei TS and AF299 to model mice further suppressed atherosclerosis compared to the administration of P. dorei TS and P. vulgatus TS. Genetic analysis of lesion tissues showed that the expression levels of genes associated with inflammatory responses were significantly reduced in mice treated with P. dorei TS and AF299. Moreover, gene expression related to immune response and IgA secretion was increased in the ileum.

Conclusion: Our results suggest that the bacteria-induced immune response in the gut leads to the suppression of the inflammatory response in atherosclerotic lesions. These results indicate the potential for the development of prophylactic drugs for atherosclerosis.

凤仙花和凤仙花通过调节肠道免疫预防动脉粥样硬化。
目的:动脉硬化是一种导致冠状动脉疾病(CAD)和中风的疾病。基础和临床研究表明,肠道微生物群与包括动脉粥样硬化在内的各种疾病之间存在联系。因此,我们专注于肠道微生物群,旨在开发一种基于益生菌的动脉粥样硬化治疗方法。方法:6 ~ 14周龄apoe缺陷小鼠作为动脉粥样硬化小鼠模型,给予多花凤梨、寻常凤梨或生理盐水灌胃5次/周。在8周龄时,饮食改为西方饮食。最后,在14周龄时处死小鼠,评估动脉粥样硬化病变面积。结果:先前的研究表明,在apoe缺陷小鼠中,给药P. dorei和P. vulgatus活型菌株(TS)可抑制动脉粥样硬化。在本研究中,我们分离到了高度表达共生定殖因子的P. vulgatus AF299。模型小鼠口服P. dorei TS和AF299与P. dorei TS和P. vulgatus TS相比,进一步抑制动脉粥样硬化。病变组织遗传分析显示,P. dorei TS和AF299治疗小鼠炎症反应相关基因的表达水平显著降低。回肠中与免疫应答和IgA分泌相关的基因表达增加。结论:我们的研究结果表明,肠道细菌诱导的免疫反应导致动脉粥样硬化病变中炎症反应的抑制。这些结果表明了开发动脉粥样硬化预防药物的潜力。
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
6.60
自引率
15.90%
发文量
271
审稿时长
1 months
期刊介绍: JAT publishes articles focused on all aspects of research on atherosclerosis, vascular biology, thrombosis, lipid and metabolism.
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