Visualizing caveolin-1 and HDL in cholesterol-loaded aortic endothelial cells

被引:20
作者
Chao, WT
Fan, SS
Chen, JK
Yang, VC
机构
[1] Tunghai Univ, Dept Biol, Taichung, Taiwan
[2] Tunghai Univ, Life Sci Res Ctr, Taichung, Taiwan
[3] Chang Gung Univ, Coll Med, Dept Physiol, Taoyuan, Taiwan
关键词
high density lipoprotein; colocalization; atherosclerosis; HIGH-DENSITY-LIPOPROTEIN; SMOOTH-MUSCLE CELLS; CELLULAR CHOLESTEROL; RAT AORTA; APOLIPOPROTEIN; MEMBRANE; EFFLUX; TRANSPORT; BINDING; TRANSLOCATION;
D O I
10.1194/jlr.M300033-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caveolae are vesicular invaginations of the plasma membranes that regulate signal transduction and transcytosis, as well as cellular cholesterol homeostasis. Our previous studies indicated that the removal of cholesterol from aortic endothelial cells and smooth muscle cells in the presence of HDL is associated with plasmalemmal invaginations; and plasmalemmal vesicles. The goal of the present study was to investigate the location and distribution of caveolin-1, the main structural protein component of caveolae, in cholesterol-loaded aortic endothelial cells after HDL incubation. Confocal microscopic analysis demonstrated that the caveolin-1 appeared to colocalize Kith HDL-fluorescein 1,1'-dioctadecyl 3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI) conjugates on the cell surface. No free HDL-DiI conjugates were revealed in the cytoplasm. Immunoelectron microscopy further demonstrated that caveolin-1 gold (15 nm) conjugates colocalized with HDL gold (10 nm) conjugates in the plasmalemmal invaginations. These morphological results indicated that caveolae are the major membrane domains facilitating the transport of excess cholesterol to HDL on the cell surface of aortic endothelial cells.
引用
收藏
页码:1094 / 1099
页数:6
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