Regulatory effects of aggregated LDL on apoptosis during foam cell formation of human peripheral blood monocytes

被引:16
作者
Kubo, N
Kikuchi, J
Furukawa, Y
Sakai, T
Ohta, H
Iwase, S
Yamada, H
Sakurabayashi, I
机构
[1] JICHI MED SCH, INST HEMATOL, DIV HEMOPOIESIS, MINAMI KAWACHI, TOCHIGI 32904, JAPAN
[2] HITACHI KOKI CO LTD, KATSUTA RES LAB, HITACHINAKA, IBARAKI 312, JAPAN
[3] JIKEI UNIV, SCH MED, DEPT MED AOTO, TOKYO 105, JAPAN
[4] JIKEI UNIV, SCH MED, INST DNA MED, TOKYO 105, JAPAN
关键词
atherosclerosis; foam cell; monocyte; apoptosis; low-density lipoprotein; CPP32;
D O I
10.1016/S0014-5793(97)00501-2
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
In order to investigate the mechanisms holy modified lipoproteins enhance foam cell formation, we cultured peripheral blood monocytes with various stimulants and examined the effects of aggregated low-density lipoprotein (agLDL) on cell viability and lipid metabolism, AgLDL could completely inhibit phorbol ester-induced apoptosis, which was accompanied by intracellular cholesterol accumulation, Suppression of apoptosis-promoting proteases, ICE and CPP32, was observed in agLDL-treated cells, This indicates that agLDL accelerates foam cell formation through inhibition of apoptosis and enhancement of lipid accumulation in activated monocytes, By contrast, apoptosis was enhanced when monocytes were cultured with agLDL and M-CSF. Intracellular cholesterol accumulation was not significant in M-CSF treated cells, This suggests that M-CSF may act anti-atherogenic through apoptotic elimination of lipid-baring macrophages and enhanced lipid turnover, Our observation supports the novel hypothesis that regulation of apoptosis may play an important role in the development of atherosclerosis. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:177 / 182
页数:6
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