Smith J B, Smith L, Brown E R, Barnes D, Sabir M A, Davis J S, Farese R V
Proc Natl Acad Sci U S A. 1984 Dec;81(24):7812-6. doi: 10.1073/pnas.81.24.7812.
Smooth muscle cells were cultured from rat thoracic aorta and labeled to a stable specific activity with 45Ca2+, myo-[2-3H]inositol, or 32Pi. The efflux of 45Ca2+ was monitored over 10-sec intervals. Angiotensin II (AII) increased the amount of 45Ca2+ lost by 5-fold in the first 10-sec interval after the addition of AII and by 10-fold in the second 10-sec interval. AII-stimulated 45Ca2+ release was blocked by the angiotensin antagonist [1-sarcosine, 8-leucine]AII and by La3+. The removal of external Ca2+ had no effect on AII-stimulated 45Ca2+ release. Depolarization with high external K+ only slightly increased 45Ca2+ efflux and had no effect on AII-induced 45Ca2+ release. AII had no effect on the initial rate of 45Ca2+ influx. These results indicate that the rapid 45Ca2+ efflux evoked by AII is probably due to the release of 45Ca2+ sequestered intracellularly rather than to an increase in the Ca2+ permeability of the plasma membrane. AII provoked rapid increases in the levels of phosphatidic acid and phosphoinositides in the cells. These increases in phospholipids were associated with increases in phospholipase C-generated inositol phosphates (tri-, di-, and mono-). It appears that AII simultaneously increases phosphoinositide hydrolysis and synthesis in vascular smooth muscle, and both phospholipid effects may contribute to inositol triphosphate generation, which was sufficiently rapid to have a role in intracellular Ca2+ mobilization.
从大鼠胸主动脉培养平滑肌细胞,并用45Ca2+、肌醇-[2-3H]肌醇或32Pi标记至稳定的比活性。每隔10秒监测45Ca2+的流出情况。添加血管紧张素II(AII)后,在第一个10秒间隔内,45Ca2+流失量增加了5倍,在第二个10秒间隔内增加了10倍。血管紧张素拮抗剂[1-肌氨酸,8-亮氨酸]AII和La3+可阻断AII刺激的45Ca2+释放。去除细胞外Ca2+对AII刺激的45Ca2+释放无影响。用高细胞外K+进行去极化仅略微增加45Ca2+流出,且对AII诱导的45Ca2+释放无影响。AII对45Ca2+流入的初始速率无影响。这些结果表明,AII引起的快速45Ca2+流出可能是由于细胞内储存的45Ca2+释放,而不是由于质膜Ca2+通透性增加。AII引起细胞内磷脂酸和磷酸肌醇水平迅速升高。这些磷脂的增加与磷脂酶C生成的肌醇磷酸(三磷酸、二磷酸和单磷酸)增加有关。似乎AII同时增加血管平滑肌中磷酸肌醇的水解和合成,这两种磷脂效应都可能导致三磷酸肌醇的产生,其速度足够快以致在细胞内Ca2+动员中起作用。