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

被引:63
作者
Wasserman, SM
Topper, JN
机构
[1] Stanford Univ, Med Ctr, Div Cardiovasc Med, Stanford, CA 94305 USA
[2] Frazier Healthcare Ventures, Palo Alto, CA USA
关键词
atherosclerosis; endothelium; gene expression; laminar shear stress; transcriptional profile;
D O I
10.1191/1358863x04vm521ra
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
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 (similar to1 - 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.
引用
收藏
页码:35 / 45
页数:11
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