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氧化应激反应性 miRNA 对 SIRT1 的调控及其在血管内皮细胞中作用的系统研究

Regulation of SIRT1 by oxidative stress-responsive miRNAs and a systematic approach to identify its role in the endothelium.

机构信息

1 Division of Biomedical Sciences, University of California , Riverside, California.

出版信息

Antioxid Redox Signal. 2013 Nov 1;19(13):1522-38. doi: 10.1089/ars.2012.4803. Epub 2013 Apr 25.

DOI:10.1089/ars.2012.4803
PMID:23477488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3797452/
Abstract

SIGNIFICANCE

Oxidative stress is a common denominator of various risk factors contributing to endothelial dysfunction and vascular diseases. Accumulated evidence suggests that sirtuin 1 (SIRT1) expression and/or activity is impaired by supraphysiological levels of oxidative stress, which in turn disrupts endothelial homeostasis.

RECENT ADVANCES

Several microRNAs (miRNAs) are induced by oxidative stress and termed as oxidative stress-responsive miRNAs. They may play a role linking the imbalanced redox state with dysregulated SIRT1.

CRITICAL ISSUES

This review summarizes recent findings on oxidative stress-responsive miRNAs and their involvement in SIRT1 regulation. Because of the unique characteristics of miRNAs, research in this new area requires an integrative approach that combines bioinformatics and experimental validation. Thus, a research strategy is discussed to identify the SIRT1-regulating miRNAs under oxidative stress and their functional outcomes in relation to endothelial dysfunction. Additionally, the miRNAs implicated in vascular diseases such as atherosclerosis and abdominal aortic aneurysms are discussed along with the translational potential and challenges of using miRNAs and its analogs as therapeutic agents.

FUTURE DIRECTIONS

Although at its infancy, research on oxidative stress-responsive miRNAs and their regulation of SIRT1 may provide new insights in understanding vascular disorders. Moreover, systematic approaches integrating in silico, in vitro, and in vivo observations can be useful tools in revealing the pathways modulating endothelial biology.

摘要

意义

氧化应激是导致内皮功能障碍和血管疾病的各种危险因素的共同因素。越来越多的证据表明,超生理水平的氧化应激会损害沉默信息调节因子 1(SIRT1)的表达和/或活性,进而破坏内皮细胞的内稳态。

最新进展

许多 microRNAs(miRNAs)被氧化应激诱导,并被称为氧化应激反应性 miRNAs。它们可能在连接失衡的氧化还原状态与失调的 SIRT1 方面发挥作用。

关键问题

这篇综述总结了最近关于氧化应激反应性 miRNAs 及其在 SIRT1 调节中的作用的发现。由于 miRNAs 的独特特性,这个新领域的研究需要结合生物信息学和实验验证的综合方法。因此,讨论了一种研究策略,以确定氧化应激下调节 SIRT1 的 miRNAs 及其与内皮功能障碍相关的功能结果。此外,还讨论了与动脉粥样硬化和腹主动脉瘤等血管疾病相关的 miRNAs,以及将 miRNAs 及其类似物用作治疗剂的转化潜力和挑战。

未来方向

尽管处于起步阶段,但对氧化应激反应性 miRNAs 及其对 SIRT1 的调节的研究可能为理解血管疾病提供新的见解。此外,整合计算机模拟、体外和体内观察的系统方法可以成为揭示调节内皮生物学途径的有用工具。

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