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Vascular microRNA-204 is remotely governed by the microbiome and impairs endothelium-dependent vasorelaxation by downregulating Sirtuin1

机译:血管microRNA-204受微生物组远程控制并通过下调Sirtuin1来损害内皮依赖性血管舒张。

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摘要

Gut microbiota promotes atherosclerosis, and vascular endothelial dysfunction, signalled by impaired endothelium-dependent vasorelaxation, is an early marker of atherosclerosis. Here we show that vascular microRNA-204 (miR-204) expression is remotely regulated by the microbiome, and impairs endothelial function by targeting the Sirtuin1 lysine deacetylase (Sirt1). MiR-204 is downregulated, while Sirt1 is upregulated, in aortas of germ-free mice. Suppression of gut microbiome with broad-spectrum antibiotics decreases miR-204, increases Sirt1 and bioavailable vascular nitric oxide, and improves endothelium-dependent vasorelaxation in mouse aortas. Antibiotics curtail aortic miR-204 upregulation, and rescue decline of aortic Sirt1 and endothelium-dependent vasorelaxation, triggered by high-fat diet feeding. Improvement of endothelium-dependent vasorelaxation by antibiotics is lost in mice lacking endothelial Sirt1. Systemic antagonism of miR-204 rescues impaired endothelium-dependent vasorelaxation and vascular Sirt1, and decreases vascular inflammation induced by high-fat diet. These findings reveal a gut microbe-vascular microRNA–Sirtuin1 nexus that leads to endothelial dysfunction.
机译:肠道菌群可促进动脉粥样硬化,而内皮依赖性血管舒张受损的信号表明血管内皮功能障碍是动脉粥样硬化的早期标志。在这里,我们显示血管microRNA-204(miR-204)的表达受微生物组远程调节,并通过靶向Sirtuin1赖氨酸脱乙酰基酶(Sirt1)损害内皮功能。在无菌小鼠的主动脉中,MiR-204被下调,而Sirt1被上调。用广谱抗生素抑制肠道微生物组可降低miR-204,增加Sirt1和可利用的血管性一氧化氮,并改善小鼠主动脉的内皮依赖性血管舒张。抗生素可抑制高脂饮食喂养引起的主动脉miR-204上调,并挽救主动脉Sirt1的下降和内皮依赖性血管舒张。缺乏内皮Sirt1的小鼠失去了通过抗生素改善内皮依赖性血管舒张的作用。 miR-204的全身拮抗作用可挽救受损的内皮依赖性血管舒张和血管Sirt1,并减少高脂饮食诱导的血管炎症。这些发现揭示了肠道微生物-血管微RNA–Sirtuin1的内在联系,可导致内皮功能障碍。

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