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内皮细胞对流体流动的适应:基因表达的体外分析及体内意义

Adaptation of the endothelium to fluid flow: in vitro analyses of gene expression and in vivo implications.

作者信息

Wasserman Scott M, Topper James N

机构信息

Division of Cardiovascular Medicine, Stanford University, Stanford, CA 94305-5406, USA.

出版信息

Vasc Med. 2004 Feb;9(1):35-45. doi: 10.1191/1358863x04vm521ra.

Abstract

Biomechanical forces generated by blood flow play an important role in the pathogenesis of vascular disease. For example, regions exposed to non-uniform shear stresses develop early atherosclerotic lesions while areas exposed to uniform shear stresses are protected. A variety of in vitro flow apparatuses have been created to apply well-characterized flow patterns to endothelial cells in an effort to dissect the cellular and molecular pathways involved in these distinct processes. Recent advances in biotechnology have permitted large-scale transcriptional profiling techniques to replace candidate gene screens and have allowed the genome-wide examination of biomechanical force-induced endothelial gene expression profiles. This review provides an overview of biomechanical force-induced modulation of endothelial phenotype. It examines the effect of sustained laminar shear stress (LSS), a type of uniform shear stress, on in vitro endothelial gene expression by synthesizing data from the early candidate gene and differential display polymerase chain reaction (PCR) approaches to the numerous, recent, high throughput functional genomic analyses. These studies demonstrate that prolonged LSS regulates the expression of only a small percentage (approximately 1-5%) of endothelial genes, and this transcriptional profile produces an endothelial phenotype that is quiescent, being protected from apoptosis, inflammation and oxidative stress. These observations provide a possible molecular mechanism for the strong correlation between patterns of blood flow and the occurrence of vascular pathologies, such as atherosclerosis, in vivo.

摘要

血流产生的生物力学力在血管疾病的发病机制中起重要作用。例如,暴露于非均匀剪切应力的区域会出现早期动脉粥样硬化病变,而暴露于均匀剪切应力的区域则受到保护。人们创建了各种体外流动装置,以便将特征明确的流动模式应用于内皮细胞,从而剖析这些不同过程中涉及的细胞和分子途径。生物技术的最新进展使得大规模转录谱分析技术能够取代候选基因筛选,并能对生物力学力诱导的内皮基因表达谱进行全基因组检测。本综述概述了生物力学力诱导的内皮细胞表型调节。通过综合早期候选基因和差异显示聚合酶链反应(PCR)方法的数据,以及众多近期高通量功能基因组分析的数据,研究了持续层流剪切应力(LSS,一种均匀剪切应力)对体外内皮基因表达的影响。这些研究表明,长时间的LSS仅调节一小部分(约1 - 5%)内皮基因的表达,这种转录谱产生的内皮细胞表型处于静止状态,可免受细胞凋亡、炎症和氧化应激的影响。这些观察结果为体内血流模式与血管病变(如动脉粥样硬化)发生之间的强相关性提供了一种可能的分子机制。

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