Su Z, Luo Z H, Niu X L, Guo Z G
Research Section of Pharmacology, Hunan Medical University, Changsha, People's Republic of China.
J Lipid Mediat Cell Signal. 1996 Dec;15(1):5-15. doi: 10.1016/s0929-7855(96)00449-x.
This study examined the influence of human high density lipoproteins (HDL) on the intracellular free calcium of cultured bovine aortic endothelial cells (BAECs). Intracellular Ca2+ concentration ([Ca2+]i) was determined by a fluorescent calcium indicator, Fura-2. It was found that, in the presence of 1 mmol/L extracellular calcium, HDL resulted in a biphasic elevation of [Ca2+]i in BAECs, consisting of an initial, transient component followed by a lower, but more sustained component. Doses of HDL from 25 to 200 micrograms protein/ml induced marked concentration-dependent elevations of [Ca2+]i in BAECs. The sustained component was abolished by deprivation of extracellular calcium or by pretreatment of endothelial cells with a calcium influx blocker, NiCl2, HDL-induced elevation of [Ca2+]i was attenuated in a concentration-dependent way by an inhibitor of calcium release, tetracaine. Repeated applications of HDL (100 micrograms protein/ml) markedly blunted the initial peak component of the calcium transient of BAECs. These results demonstrate that both intracellular and extracellular calcium pools are responsible for the biphasic elevation of [Ca2+]i induced by HDL in cultured BAECs.
本研究检测了人高密度脂蛋白(HDL)对培养的牛主动脉内皮细胞(BAECs)细胞内游离钙的影响。细胞内Ca2+浓度([Ca2+]i)通过荧光钙指示剂Fura-2进行测定。研究发现,在存在1 mmol/L细胞外钙的情况下,HDL导致BAECs中[Ca2+]i呈双相升高,包括一个初始的、短暂的成分,随后是一个较低但更持久的成分。25至200微克蛋白质/毫升的HDL剂量可诱导BAECs中[Ca2+]i出现明显的浓度依赖性升高。通过剥夺细胞外钙或用钙内流阻滞剂NiCl2预处理内皮细胞,可消除该持久成分,HDL诱导的[Ca2+]i升高可被钙释放抑制剂丁卡因以浓度依赖性方式减弱。重复应用HDL(100微克蛋白质/毫升)可显著减弱BAECs钙瞬变的初始峰值成分。这些结果表明,细胞内和细胞外钙库均参与了HDL在培养的BAECs中诱导的[Ca2+]i双相升高。