Center for Thrombosis and Hemostasis, University Medical Center Mainz, Johannes Gutenberg University of Mainz, Mainz, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site RheinMain, Mainz, Germany.
Eur J Immunol. 2018 Apr;48(4):564-575. doi: 10.1002/eji.201646879. Epub 2018 Jan 19.
Commensal gut microbiota have recently been implicated in cardiovascular disease (CVD) and cerebrovascular disease. Atherosclerotic plaque formation depends on the colonization status of the host. In addition to host nutrition and the related microbiota-dependent metabolic changes, activation of innate immune pathways triggers the development of atherosclerosis and supports arterial thrombosis. Gnotobiotic mouse models have uncovered that activation of Toll-like receptor-2 by gut microbial ligands supports von Willebrand factor-integrin mediated platelet deposition to the site of vascular injury. Depending on nutritional factors, the microbiota-derived choline-metabolite trimethylamine N-oxide (TMAO) increases atherosclerotic plaque size, triggers prothrombotic platelet function and promotes arterial thrombus growth. Hence, the composition of the commensal microbiota is an emerging risk factor for CVD. Here, we provide an overview on microbiota-dependent pathomechanisms that drive the development of CVD and arterial thrombosis.
肠道共生菌群最近被牵连到心血管疾病 (CVD) 和脑血管疾病中。动脉粥样硬化斑块的形成取决于宿主的定植状态。除了宿主营养和相关的依赖于微生物群的代谢变化外,先天免疫途径的激活会引发动脉粥样硬化的发展,并支持动脉血栓形成。无菌小鼠模型揭示,肠道微生物配体激活 Toll 样受体 2 可支持血管损伤部位 von Willebrand 因子-整合素介导的血小板沉积。根据营养因素的不同,微生物衍生的胆碱代谢物三甲胺 N-氧化物 (TMAO) 会增加动脉粥样硬化斑块的大小,引发促血栓形成的血小板功能,并促进动脉血栓的生长。因此,共生菌群的组成是 CVD 的一个新出现的危险因素。在这里,我们提供了一个关于依赖于微生物群的病理机制的概述,这些机制驱动了 CVD 和动脉血栓形成的发展。