Lampugnani M G, Pedehovi M, Dejana E, Rotilio D, Donati M B, Bussolino F, Garbarino G, Ghigo D, Bosia A
Istituto Mario Negri, Milano, Italy.
Thromb Res. 1989 Apr 1;54(1):75-87. doi: 10.1016/0049-3848(89)90338-1.
This report shows that purified human alpha-thrombin was able to stimulate a rapid and transient formation of water-soluble phosphorylated 3H-inositols in cultured human umbilical vein endothelial cells (HUVEC) prelabelled with 3H-inositol. A parallel breakdown and resynthesis of 3H-inositol-containing phospholipids was observed. Simultaneously, thrombin induced a transient increase of intracellular free Ca2+[( Ca2+]i), as measured from increased fluorescence of quin2 loaded cells. Phosphoinositide turnover and Ca2+ mobilization showed a similar dependence on thrombin dose. [Ca2+]i rise resulted from both influx from extracellular medium and redistribution from intracellular storage sites. On the other hand thrombin-induced phosphoinositide hydrolysis was not dependent on [Ca2+]i rise. [Ca2+]i elevation might be, at least partially, a consequence of increased phosphoinositide turnover, as suggested by [Ca2+]-mobilizing activity of inositol-trisphosphate in other cells.
本报告表明,纯化的人α-凝血酶能够刺激预先用³H-肌醇标记的培养人脐静脉内皮细胞(HUVEC)中水溶性磷酸化³H-肌醇的快速瞬时形成。观察到含³H-肌醇的磷脂同时发生分解和重新合成。同时,凝血酶诱导细胞内游离Ca²⁺([Ca²⁺]i)瞬时增加,这是通过测量负载quin2的细胞荧光增强来测定的。磷酸肌醇代谢和Ca²⁺动员对凝血酶剂量表现出相似的依赖性。[Ca²⁺]i升高是细胞外介质流入和细胞内储存部位重新分布共同作用的结果。另一方面,凝血酶诱导的磷酸肌醇水解不依赖于[Ca²⁺]i升高。正如其他细胞中肌醇三磷酸的[Ca²⁺]动员活性所表明的,[Ca²⁺]i升高可能至少部分是磷酸肌醇代谢增加的结果。