Division of Cardiology, Department of Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
Am J Physiol Heart Circ Physiol. 2024 Dec 1;327(6):H1361-H1375. doi: 10.1152/ajpheart.00267.2024. Epub 2024 Oct 25.
The global population of individuals with cardiovascular disease is expanding, and a key risk factor for major adverse cardiovascular events is vascular calcification. The pathogenesis of cardiovascular calcification is complex and multifaceted, with external cues driving epigenetic, transcriptional, and metabolic changes that promote vascular calcification. This review provides an overview of some of the lesser understood molecular processes involved in vascular calcification and discusses the links between calcification pathogenesis and aspects of adenosine signaling and the methionine pathway; the latter of which salvages the essential amino acid methionine, but also provides the substrate critical for methylation, a modification that regulates the function and activity of DNA and proteins. We explore the complex and dynamic nature of osteogenic reprogramming underlying intimal atherosclerotic calcification and medial arterial calcification (MAC). Atherosclerotic calcification is more widely studied; however, emerging studies now show that MAC is a significant pathology independent from atherosclerosis. Furthermore, we emphasize metabolite and metabolic-modulating factors that influence vascular calcification pathogenesis. Although the contributions of these mechanisms are more well-define in relation to atherosclerotic intimal calcification, understanding these pathways may provide crucial mechanistic insights into MAC and inform future therapeutic approaches. Herein, we highlight the significance of adenosine and methyltransferase pathways as key regulators of vascular calcification pathogenesis.
心血管疾病患者的全球人口正在不断增加,而主要不良心血管事件的一个关键风险因素是血管钙化。心血管钙化的发病机制复杂且多方面,外部线索驱动着表观遗传、转录和代谢变化,促进血管钙化。这篇综述概述了一些在血管钙化中涉及的不太为人知的分子过程,并讨论了钙化发病机制与腺苷信号和蛋氨酸途径之间的联系;后者可挽救必需氨基酸蛋氨酸,但也提供了甲基化的关键底物,这种修饰可调节 DNA 和蛋白质的功能和活性。我们探讨了动脉粥样硬化钙化和中层动脉钙化(MAC)中骨生成重编程的复杂和动态性质。动脉粥样硬化钙化的研究更为广泛,但新兴的研究表明,MAC 是一种独立于动脉粥样硬化的重要病理学。此外,我们强调了影响血管钙化发病机制的代谢物和代谢调节因子。尽管这些机制在与动脉粥样硬化内膜钙化的关系中更为明确,但了解这些途径可能为 MAC 提供关键的机制见解,并为未来的治疗方法提供信息。在此,我们强调了腺苷和甲基转移酶途径作为血管钙化发病机制关键调节剂的重要性。