心血管疾病中嘌呤能信号对转录因子功能的调控。

IF 3 4区 医学 Q2 NEUROSCIENCES
Hao Tang, Qihang Kong, Zhewei Zhang, Wenchao Wu, Lixing Yuan, Xiaojing Liu
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引用次数: 0

摘要

心血管疾病(CVDs),包括高血压、动脉粥样硬化、心肌缺血和心肌梗塞,是全球死亡的主要原因。转录因子在心血管疾病的发病过程中起着关键作用,并通过协调涉及炎症、氧化应激、血管生成和糖代谢的许多基因的转录,促进这些疾病的病理生理学发展。在健康和病理环境中,止血的一个重要调节因子已被确定为嘌呤能信号通路。研究表明,与心血管疾病病理生理学有关的几个信号网络是由受嘌呤能物质调控的转录因子形成的。在此,我们简要总结了受嘌呤能通路调控的转录因子在各类心血管疾病中的作用和机制。这些信息对于发现治疗和预防心血管疾病的新方法至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Regulation of transcription factor function by purinergic signalling in cardiovascular diseases.

Regulation of transcription factor function by purinergic signalling in cardiovascular diseases.

Cardiovascular diseases (CVDs), including hypertension, atherosclerosis, myocardial ischemia, and myocardial infarction, constitute the primary cause of mortality worldwide. Transcription factors play critical roles in the development of CVDs and contribute to the pathophysiology of these diseases by coordinating the transcription of many genes involved in inflammation, oxidative stress, angiogenesis, and glycolytic metabolism. One important regulator of hemostasis in both healthy and pathological settings has been identified as a purinergic signalling pathway. Research has demonstrated that several signalling networks implicated in the pathophysiology of CVDs are formed by transcription factors that are regulated by purinergic substances. Here, we briefly summarize the roles and mechanisms of the transcription factors regulated by purinergic pathways in various types of CVD. This information will be essential for discovering novel approaches for CVD treatment and prevention.

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来源期刊
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
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