Concentration Polarization of Oxidative Modification of Low-Density Lipoproteins: Its Effect on Oxidative Modification of Low-Density Lipoprotein Uptake and Apoptosis of the Endothelial Cells

被引:4
|
作者
Ding, Zufeng [1 ]
Fan, Yubo [1 ]
Deng, Xiaoyan [1 ]
机构
[1] Beihang Univ, Sch Biol Sci & Med Engn, Minist Educ, Key Lab Biomech & Mechanobiol, Beijing 100191, Peoples R China
关键词
OX-LDL RECEPTOR-1; SMOOTH-MUSCLE CELLS; LECTIN-LIKE; OXIDIZED LDL; LUMINAL SURFACE; TNF-ALPHA; ATHEROSCLEROSIS; LOX-1; ATHEROGENESIS; ACTIVATION;
D O I
10.1097/MAT.0b013e3181e7be08
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There is increasing evidence suggesting that oxidative modification of low-density lipoprotein (ox-LDL) in the vessel wall plays a crucial role in the initiation and progression of atherogenesis. The purpose of this study is to substantiate our hypothesis that concentration polarization of ox-LDL may also occur in the arterial system, which in turn can lead to enhanced endothelial cell (EC) apoptosis and induce atherogenesis. Using a parallel-plate flow chamber technique, ox-LDL uptake and apoptosis of the human ECs cultured on permeable or nonpermeable membranes were analyzed. The experimental results showed that 1,1'-dioctadecyl-3,3,3',3'-tetramethyl indocarbocyanine (DiI)-ox-LDL uptake by the ECs increased with increasing concentration of DiI-ox-LDL in the perfusion solution. The overall average value of DiI-ox-LDL uptake was similar to 20% higher for the permeable group than that for the nonpermeable group. The results also showed that ox-LDL induced ECs death and apoptosis in the permeable group were similar to 12% and 26% higher than those in the nonpermeable group, respectively. The results from the in vitro model study, therefore, support our hypothesis that concentration polarization of ox-LDLs may occur in the arterial system. In conclusion, the occurrence of ox-LDL concentration polarization could enhance ox-LDL infiltration into the arterial wall and accelerate EC apoptosis. ASAIO Journal 2010; 56:468-474.
引用
收藏
页码:468 / 474
页数:7
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