作者: G Ku , C.E. Thomas , A.L. Akeson , R.L. Jackson
DOI: 10.1016/S0021-9258(19)49695-6
关键词: Lipid oxidation 、 Cytokine 、 Endothelial stem cell 、 Interleukin 、 Molecular biology 、 Vascular smooth muscle 、 Biochemistry 、 Cell growth 、 Foam cell 、 Biology 、 Cholesteryl ester
摘要: Oxidatively modified low density lipoproteins (LDL) have recently been proposed to play a role in atherogenesis by promoting foam cell formation and endothelial toxicity. The purpose of the present study was determine whether LDL could also induce macrophage release interleukin 1 beta (IL-1 beta), cytokine which enhances vascular smooth muscle proliferation, another feature atherosclerotic process. were oxidatively incubation with either Cu2+ (Cu(2+)-LDL) or human peripheral blood monocyte-derived macrophages (M-LDL). Incubation these (6 x 10(6) cells/culture) resulted dose-dependent induction IL-1 release. At 300 micrograms protein/ml, Cu(2+)-LDL M-LDL induced 422 333 pg beta/culture, respectively. Saponified shown contain 9- 13-hydroxyoctadecadienoic acid (HODE), lipid oxidation products linoleate. When tested for activity culture (3 cells/culture), it found that 9-HODE 13-HODE (final concentration 33 microM) 122 43 respectively, whereas untreated cells released only 4 beta/culture. cholesteryl-9-HODE release; however, degree its cholesteryl ester relative suggests other components oxidized may contribute induction. rapidly taken up macrophages, kinetics similar A 1.5- 6-fold increase level mRNA detected as little 3-h post-9-HODE treatment. from LDL, associated linoleate products, proliferation.