YAP/TAZ是心血管生理调节和发病机制中的机械生物学信号通路

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摘要

心血管疾病(CVDs)一直是全球过早死亡和患病的主要原因。Hippo信号通路因其高度保守的性质以及在调节器官大小、组织稳态和干细胞功能方面不可或缺的作用而闻名,已被确定为心血管疾病发病机制中的一个关键因素。最近的发现强调了Yes相关蛋白(YAP)和具有PDZ结合基调的转录激活子(TAZ)(统称为YAP/TAZ)的重要性。这些蛋白作为 Hippo 通路的下游成分,在心血管发育和稳态调节中发挥着关键作用。YAP/TAZ可通过与转录因子,尤其是转录增强子关联结构域(TEAD)家族中的转录因子相互作用,调控细胞增殖、迁移、分化和凋亡等各种细胞过程。本综述旨在全面概述目前对心血管生理学和发病机理中 YAP/TAZ 信号转导的理解。我们分析了 YAP/TAZ 激活的调控机制,探讨了它们的下游效应因子,并研究了它们与心血管疾病的关联,包括心肌肥厚、心肌梗塞、肺动脉高压、心肌缺血再灌注损伤、动脉粥样硬化、血管生成、再狭窄和心脏纤维化。此外,我们还探讨了靶向 YAP/TAZ 通路治疗心血管疾病的潜在治疗意义。通过这篇综述,我们旨在阐明目前对心血管生物学中 YAP/TAZ 信号转导的理解,并强调其对心血管疾病诊断和治疗干预的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

YAP/TAZ as mechanobiological signaling pathway in cardiovascular physiological regulation and pathogenesis

YAP/TAZ as mechanobiological signaling pathway in cardiovascular physiological regulation and pathogenesis

Cardiovascular diseases (CVDs) persistently rank as a leading cause of premature death and illness worldwide. The Hippo signaling pathway, known for its highly conserved nature and integral role in regulating organ size, tissue homeostasis, and stem cell function, has been identified as a critical factor in the pathogenesis of CVDs. Recent findings underscore the significance of the Yes-associated protein (YAP) and the Transcriptional Coactivator with PDZ-binding motif (TAZ), collectively referred to as YAP/TAZ. These proteins play pivotal roles as downstream components of the Hippo pathway, in the regulation of cardiovascular development and homeostasis. YAP/TAZ can regulate various cellular processes such as cell proliferation, migration, differentiation, and apoptosis through their interactions with transcription factors, particularly those within the transcriptional enhancer associate domain (TEAD) family. The aim of this review is to provide a comprehensive overview of the current understanding of YAP/TAZ signaling in cardiovascular physiology and pathogenesis. We analyze the regulatory mechanisms of YAP/TAZ activation, explore their downstream effectors, and examine their association across numerous cardiovascular disorders, including myocardial hypertrophy, myocardial infarction, pulmonary hypertension, myocardial ischemia-reperfusion injury, atherosclerosis, angiogenesis, restenosis, and cardiac fibrosis. Furthermore, we investigate the potential therapeutic implications of targeting the YAP/TAZ pathway for the treatment of CVDs. Through this comprehensive review, our aim is to elucidate the current understanding of YAP/TAZ signaling in cardiovascular biology and underscore its potential implications for the diagnosis and therapeutic intervention of CVDs.

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