Wolfovitz E, Aviram M, Brook J G, Tatarsky I, Lanir N
Department of hematology, Rambam Medical Center, Haifa, Israel.
J Cardiovasc Risk. 1995 Feb;2(1):57-62.
Increasing evidence suggests that oxidized low-density lipoprotein (LDL) is associated with the development of atherosclerosis in vivo. Because endothelial injury contributes to the development of the atherogenic , we investigated the efficacy of oxidized LDL on the integrity of human umbilical cord endothelial cells (HUVECs) by analyzing cytotoxicity and cell detachment.
The cellular integrity of cultured endothelial cells labeled with chromium-51.
Low concentrations of oxidized LDL (25-50 micrograms protein/ml) induced morphological changes (cell elongation and formation of gaps in the cobblestone monolayer), decreased cellular cytotoxicity (by 13% compared with control). At higher concentrations of oxidized LDL (100 micrograms protein/ml), however, increases in cytotoxicity (by up to 70%) and cellular detachment (by up to 90%) were demonstrated. Native LDL, which was not oxidized in out cell system, did not induce any changes either in cytotoxicity or in cell detachment. The protective effect of low oxidized LDL concentrations against endothelial cell cytotoxicity and detachment was abolished by indomethacin (microM), indicating the involvement or prostaglandin synthesis in this protection.
Our experiments suggest that oxidized LDL-induced alterations of endothelial cells involve a sequence of events leading from a non-cytotoxic protective stage to endothelial perturbation.
越来越多的证据表明,氧化型低密度脂蛋白(LDL)在体内与动脉粥样硬化的发展相关。由于内皮损伤促成动脉粥样硬化的发展,我们通过分析细胞毒性和细胞脱离情况,研究了氧化型LDL对人脐静脉内皮细胞(HUVECs)完整性的影响。
用51铬标记培养的内皮细胞的细胞完整性。
低浓度的氧化型LDL(25 - 50微克蛋白质/毫升)可诱导形态学变化(细胞伸长及鹅卵石样单层细胞出现间隙),降低细胞毒性(与对照组相比降低13%)。然而,在较高浓度的氧化型LDL(100微克蛋白质/毫升)时,细胞毒性增加(高达70%),细胞脱离增加(高达90%)。在我们的细胞体系中未被氧化的天然LDL,在细胞毒性或细胞脱离方面均未诱导任何变化。低浓度氧化型LDL对内皮细胞毒性和脱离的保护作用被吲哚美辛(微摩尔)消除,表明前列腺素合成参与了这种保护作用。
我们的实验表明,氧化型LDL诱导的内皮细胞改变涉及一系列事件,从非细胞毒性保护阶段到内皮细胞紊乱。