Hallam T J, Thompson N T, Scrutton M C, Rink T J
Biochem J. 1984 Aug 1;221(3):897-901. doi: 10.1042/bj2210897.
Responses to vasopressin were studied in human platelets loaded with the fluorescent Ca2+ indicator, quin2. In the presence of 1 mM external Ca2+, vasopressin caused a transient rise in [Ca2+]i from the basal level near 100nM to about 700 nM; peak [Ca2+]i was reached in a few seconds and the level then declined towards resting over several minutes. In the absence of external Ca2+ there was a much smaller rise of similar time-course, suggesting that vasopressin increases [Ca2+]i mainly by stimulated-influx across the plasma membrane but also by partly releasing internal Ca2+. Inhibition of thromboxane A2 formation somewhat reduced the peak [Ca2+]i in the presence of external Ca2+, but had no effect on the response attributed to release of internal Ca2+. With external Ca2+, vasopressin stimulated shape-change, secretion and aggregation. Secretion and aggregation were decreased by about half following blockage of thromboxane production. The ability of vasopressin to induce shape-change and secretion even at near basal [Ca2+]i suggests that activators other than Ca2+ are involved.
使用装载了荧光钙离子指示剂喹啉-2的人血小板研究了对血管加压素的反应。在存在1 mM细胞外钙离子的情况下,血管加压素使细胞内钙离子浓度([Ca2+]i)从接近100 nM的基础水平短暂升高至约700 nM;几秒钟内达到[Ca2+]i峰值,随后在几分钟内降至静息水平。在不存在细胞外钙离子的情况下,类似时间进程的升高幅度要小得多,这表明血管加压素增加[Ca2+]i主要是通过刺激钙离子跨质膜内流,但也有部分是通过释放细胞内钙离子。抑制血栓素A2的形成在存在细胞外钙离子的情况下会稍微降低[Ca2+]i峰值,但对归因于细胞内钙离子释放的反应没有影响。在有细胞外钙离子的情况下,血管加压素刺激形状改变、分泌和聚集。血栓素生成受阻后,分泌和聚集减少约一半。血管加压素即使在接近基础[Ca2+]i时也能诱导形状改变和分泌,这表明除了钙离子之外还有其他激活剂参与其中。