Division of Cardiology, Department of Internal Medicine and Cardiovascular Center, National Taiwan University Hospital, Taipei 100, Taiwan.
Department and Graduate Institute of Pharmacology, College of Medicine, National Taiwan University, Taipei 100, Taiwan.
Int J Mol Sci. 2020 Nov 19;21(22):8729. doi: 10.3390/ijms21228729.
Inflammation is the key for the initiation and progression of atherosclerosis. Accumulating evidence has revealed that an altered gut microbiome (dysbiosis) triggers both local and systemic inflammation to cause chronic inflammatory diseases, including atherosclerosis. There have been some microbiome-relevant pro-inflammatory mechanisms proposed to link the relationships between dysbiosis and atherosclerosis such as gut permeability disruption, trigger of innate immunity from lipopolysaccharide (LPS), and generation of proatherogenic metabolites, such as trimethylamine N-oxide (TMAO). Meanwhile, immune responses, such as inflammasome activation and cytokine production, could reshape both composition and function of the microbiota. In fact, the immune system delicately modulates the interplay between microbiota and atherogenesis. Recent clinical trials have suggested the potential of immunomodulation as a treatment strategy of atherosclerosis. Here in this review, we present current knowledge regarding to the roles of microbiota in contributing atherosclerotic pathogenesis and highlight translational perspectives by discussing the mutual interplay between microbiota and immune system on atherogenesis.
炎症是动脉粥样硬化发生和发展的关键。越来越多的证据表明,肠道微生物组的改变(失调)会引发局部和全身炎症,导致慢性炎症性疾病,包括动脉粥样硬化。已经提出了一些与微生物组相关的促炎机制来联系失调与动脉粥样硬化之间的关系,例如肠道通透性破坏、内毒素(LPS)引发固有免疫和产生促动脉粥样硬化代谢物,如三甲胺 N-氧化物(TMAO)。同时,免疫反应,如炎症小体激活和细胞因子产生,可以重塑微生物组的组成和功能。事实上,免疫系统巧妙地调节了微生物组与动脉粥样硬化发生之间的相互作用。最近的临床试验表明,免疫调节作为动脉粥样硬化治疗策略的潜力。在这篇综述中,我们介绍了微生物组在促进动脉粥样硬化发病机制中的作用的最新知识,并通过讨论微生物组和免疫系统在动脉粥样硬化发生中的相互作用,强调了转化研究的观点。