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储存期间血小板亚群中凝血酶诱导的钙离子动员丧失。

Loss of thrombin-induced Ca2+ mobilization in a subpopulation of platelets during storage.

作者信息

Fijnheer R, Homburg C H, Hooibrink B, Boomgaard M N, de Korte D, Roos D

机构信息

Central Laboratory of the Netherlands Red Cross Blood Transfusion Service, Amsterdam.

出版信息

Thromb Haemost. 1991 Sep 2;66(3):350-4.

PMID:1746007
Abstract

Thrombin-induced changes in cytosolic free Ca2+ ([Ca2+]i) were studied in human platelets that had been stored for up to 6 days. Changes in [Ca2+]i were measured with Indo-1-loaded platelets and quantitated with two different methods: (i) measurement of the changes in total fluorescence; (ii) measurement of the [Ca2+]i changes in individual platelets in a flow cytometer, allowing the detection of non-responding platelets. The maximal concentration of [Ca2+]i after stimulation with 0.5 U of thrombin/ml decreased from 544 +/- 58 nM (mean +/- SEM, n = 6) on day 0, to 276 +/- 9 nM on day 3 and to 203 +/- 23 nM on day 6. The percentage of platelets responding to 0.5 U of thrombin/ml declined from 90 +/- 2% on day 0 to 72 +/- 4% on day 3, and to 47 +/- 8% on day 6. Nevertheless, also the responding platelets showed a decreased rise in [Ca2+]i. The study shows that during platelet storage a decrease in the rise in [Ca2+]i upon thrombin stimulation occurs. This decrease is partly due to the formation of a subpopulation of platelets that is completely unresponsive and partly due to a decreased responsiveness in the remainder of the platelets; it is not due to a gradual decline in [Ca2+]i rise in all platelets. This phenomenon provides new insight in the functional defect of stored platelets.

摘要

研究了储存长达6天的人血小板中凝血酶诱导的细胞溶质游离钙([Ca2+]i)变化。用负载Indo-1的血小板测量[Ca2+]i变化,并用两种不同方法进行定量:(i)测量总荧光变化;(ii)在流式细胞仪中测量单个血小板的[Ca2+]i变化,从而能够检测无反应的血小板。用0.5 U/ml凝血酶刺激后,[Ca2+]i的最大浓度从第0天的544±58 nM(平均值±标准误,n = 6)降至第3天的276±9 nM,第6天降至203±23 nM。对0.5 U/ml凝血酶有反应的血小板百分比从第0天的90±2%降至第3天的72±4%,第6天降至47±8%。然而,有反应的血小板的[Ca2+]i升高也有所降低。该研究表明,在血小板储存期间,凝血酶刺激后[Ca2+]i的升高会降低。这种降低部分是由于形成了完全无反应的血小板亚群,部分是由于其余血小板的反应性降低;并非由于所有血小板中[Ca2+]i升高逐渐下降。这一现象为储存血小板的功能缺陷提供了新的见解。

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