Johnson P C, Ware J A, Salzman E W
Thromb Res. 1985 Nov 15;40(4):435-43. doi: 10.1016/0049-3848(85)90280-4.
Platelet aggregation and aequorin-indicated cytoplasmic ionized calcium concentration ([Cai2+]) were measured simultaneously using a modification of a commercially available instrument, the Chronolog Whole Blood Lumiaggregometer. The [Cai2+] rise in response to arachidonic acid, the Ca2+-ionophore A23187, collagen, and epinephrine occurred either before or simultaneously with platelet shape change or aggregation. PGD2 caused concentration-dependent inhibition of both the [Cai2+] rise and aggregation. However, suppression of the [Cai2+] rise alone did not fully account for the inhibition of aggregation due to the elevated cAMP produced by PGD2. Agonist-induced elevation of [Cai2+] did not depend on platelet aggregation, but was enhanced by close platelet-to-platelet contact. Concurrent measurement of platelet aggregation and [Cai2+] may further clarify pathways to platelet activation.
使用市售仪器Chronolog全血发光聚集仪的改良版,同时测量血小板聚集和水母发光蛋白指示的细胞质游离钙浓度([Cai2+])。对花生四烯酸、钙离子载体A23187、胶原蛋白和肾上腺素的反应中,[Cai2+]的升高发生在血小板形态改变或聚集之前或同时。PGD2导致[Cai2+]升高和聚集的浓度依赖性抑制。然而,单独抑制[Cai2+]升高并不能完全解释由于PGD2产生的cAMP升高对聚集的抑制作用。激动剂诱导的[Cai2+]升高不依赖于血小板聚集,但紧密的血小板间接触会增强这种升高。同时测量血小板聚集和[Cai2+]可能会进一步阐明血小板激活的途径。