Metabolites and metabolism in vascular calcification: links between adenosine signaling and the methionine cycle.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Parya Behzadi, Cynthia St Hilaire
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引用次数: 0

Abstract

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.

血管钙化中的代谢物和代谢:腺苷信号与蛋氨酸循环之间的联系。
全球心血管疾病患者人数不断增加,而血管钙化是导致重大不良心血管事件的一个关键风险因素。心血管钙化的发病机制复杂而多面,外部线索驱动表观遗传、转录和代谢变化,从而促进血管钙化。本综述概述了参与血管钙化的一些鲜为人知的分子过程,并讨论了钙化发病机制与腺苷信号转导和蛋氨酸途径之间的联系;后者不仅能挽救必需氨基酸蛋氨酸,还能提供甲基化的关键底物,而甲基化是一种调节 DNA 和蛋白质功能和活性的修饰。我们探讨了动脉粥样硬化内膜钙化和动脉内膜钙化(MAC)背后复杂而动态的成骨细胞重编程。动脉粥样硬化性钙化的研究更为广泛,但新的研究表明,内侧动脉钙化是一种独立于动脉粥样硬化的重要病理现象。此外,我们还强调了影响血管钙化发病机制的代谢物和代谢调节因素。虽然这些机制对动脉粥样硬化内膜钙化的影响更为明确,但了解这些途径可能会对 MAC 提供重要的机理认识,并为未来的治疗方法提供依据。在此,我们强调腺苷和甲基转移酶途径作为血管钙化发病机制关键调节因子的重要性。
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
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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