Oxidized-LDL induce morphological changes and increase stiffness of endothelial cells

被引:70
作者
Chouinard, Julie A. [1 ,2 ]
Grenier, Guillaume [2 ,3 ]
Khalil, Abdelouahed [2 ,4 ]
Vermette, Patrick [1 ,2 ]
机构
[1] Univ Sherbrooke, Dept Chem Engn, Lab Bioingn & Biophys, Sherbrooke, PQ J1K 2R1, Canada
[2] Sherbrooke Geriatr Univ Inst, Res Ctr Aging, Sherbrooke, PQ, Canada
[3] Univ Sherbrooke, Fac Med, Dept Surg, Serv Orthopaed, Sherbrooke, PQ J1K 2R1, Canada
[4] Univ Sherbrooke, Fac Med, Dept Med, Serv Geriatry, Sherbrooke, PQ J1K 2R1, Canada
关键词
atomic force microscopy; AFM; HUVEC; LDL; ox-LDL; endothelial dysfunction; cell rigidity; cytoskeleton;
D O I
10.1016/j.yexcr.2008.07.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There is increasing evidence suggesting that oxidized low-density lipoproteins (ox-LDL) play a Critical role in endothelial injury contributing to the age-related physio-pathological process of atherosclerosis. In this Study, the effects of native LDL and ox-LDL on the mechanical properties of living human umbilical vein endothelial cells (HUVEC) were investigated by atomic force microscopy (AFM) force measurements. The contribution of filamentous actin (F-actin) and vimentin on cytoskeletal network Organization were also examined by fluorescence microscopy. Our results revealed that ox-LDL had an impact on the HUVEC shape by interfering with F-actin and vimentin while native LDL showed no effect. AFM colloidal force measurements on living individual HUVEC were successfully used to measure stiffness of cells exposed to native and ox-LDL. AFM results demonstrated that the cell body became significantly stiffer when cells were exposed for 24 h to ox-LDL while cells exposed for 24 h to native LDL displayed similar rigidity to that of the control cells. Young's moduli of LDL-exposed HUVEC were calculated using two models. This study thus provides quantitative evidence on biomechanical mechanisms related to endothelial cell dysfunction and may give new insight on strategies aiming to protect endothelial function in atherosclerosis. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:3007 / 3016
页数:10
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