Lipoproteins modify the macrophage uptake of triacylglycerol emulsion and of zymosan particles by similar mechanisms

被引:8
作者
Carvalho, MDT
Tobias, VE
Vendrame, CMV
Shimabukuro, AF
Gidlund, M
Quintao, ECR
机构
[1] Univ Sao Paulo, Lipids Lab LIM 10, Sch Med, BR-01246903 Sao Paulo, Brazil
[2] Univ Sao Paulo, Schistosomiasis Immunopathol Lab LIM 06, Sch Med, BR-01246903 Sao Paulo, Brazil
[3] Univ Sao Paulo, Dept Pathol, Sch Med, BR-01246903 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
D O I
10.1007/s11745-000-0494-1
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
The uptake of lipids and formation of foam cells are key events in atherosclerosis and in eruptive xanthomata formation in primary hyperchylomicronemia. Here we have compared the influence of low density lipoprotein (LDL), oxidized LDL (oxLDL), high density lipoprotein (HDL), and delipidated:HDL (apoHDL) on the uptake by macrophages of zymosan tan insoluble fraction of yeast cell walls) and of triglyceride rich emulsion (EM) particles that resemble chylomicrons, but, like zymosan, are equally devoid of protein components. Zymosan internalization is known to occur through unspecific phagocytosis,whereas natural chylomicrons are taken up by several specific lipoprotein receptors. We found that phagocytosis is not promoted as much by oxLDL as by normal LDL. HDL-coated zymosan was found to be inert and apoHDL slightly enhanced phagocytosis. LDL and apoHDL promoted the uptake of EM while oxLDL and HDL significantly inhibited the uptake. Therefore, the data support that HDL, and not apoHDL, particles inhibit EM uptake. We concluded that by using lipoprotein-coated zymosan particles, we could demonstrate different biological effects of LDL, oxLDL, HDL, and apoHDL on macrophage phagocytosis and that this method could be useful to delineate components of the various lipoproteins important for the propagation or inhibition of the formation of foam cells.
引用
收藏
页码:55 / 59
页数:5
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