Hemodynamic shear stresses in mouse aortas - Implications for atherogenesis

被引:240
作者
Suo, Jin
Ferrara, Dardo E.
Sorescu, Dan
Guldberg, Robert E.
Taylor, W. Robert
Giddens, Don P.
机构
[1] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
[3] Emory Univ, George W Woodruff Sch Mech Engn, Atlanta, GA 30322 USA
[4] Emory Univ, Div Cardiol, Atlanta, GA 30322 USA
[5] Atlanta VA Med Ctr, Atlanta, GA USA
关键词
atherosclerosis; wall shear stress; computational fluid dynamics; micro CT; two-photon microscopy; adhesion molecules;
D O I
10.1161/01.ATV.0000253492.45717.46
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-The hemodynamic environment is a determinant of susceptibility to atherosclerosis in the vasculature. Although mouse models are commonly used in atherosclerosis studies, little is known about local variations in wall shear stress (WSS) in the mouse and whether the levels of WSS are comparable to those in humans. The objective of this study was to determine WSS values in the mouse aorta and to relate these to expression of gene products associated with atherosclerosis. Methods and Results-Using micro-CT and ultrasound methodologies we developed a computational fluid dynamics model of the mouse aorta and found values of WSS to be much larger than those for humans. We also used a quantum dot-based approach to study vascular cell adhesion molecule-1 and intercellular adhesion molecule-1 expression on the aortic intima and demonstrated that increased expression for these molecules occurs where WSS was relatively low for the mouse. Conclusions-Despite large differences in WSS in the two species, the spatial distributions of atherogenic molecules in the mouse aorta are similar to atherosclerotic plaque localization found in human aortas. These results suggest that relative differences in WSS or in the direction of WSS, as opposed to the absolute magnitude, may be relevant determinants of flow-mediated inflammatory responses.
引用
收藏
页码:346 / 351
页数:6
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