Verhoeven A J, Mommersteeg M E, Akkerman J W
Biochem J. 1984 Aug 1;221(3):777-87. doi: 10.1042/bj2210777.
The involvement of metabolic energy in platelet responses was investigated by measuring the energy consumption during aggregation and secretion from dense, alpha- and acid-hydrolase-containing granules. Gel-filtered human platelets were stimulated with different amounts of thrombin (0.05-5.0 units X ml-1). At various stages during aggregation and secretion the energy consumption was measured from the changes in metabolic ATP and ADP following abrupt arrest of ATP resynthesis. Stimulation with 5 units of thrombin X ml-1 increased the energy consumption from 6.2 +/- 0.9 to 17.8 +/- 0.4 mumol of ATPeq. X min-1 X (10(11) platelets)-1 during the first 15 s. It decreased thereafter and returned to values found in resting cells after about 30 s. With 0.05 unit of thrombin X ml-1, the energy consumption accelerated more slowly and took at least 3 min before it normalized. A strong positive correlation was found between the velocities of the three secretion responses and the concurrent energy consumption (a) at different stages of the responses induced by a given dose of thrombin, and (b) at different secretion velocities initiated by different amounts of thrombin. When, at different stages of the responses, the extent of secretion was compared with the amount of energy that had been consumed, a strong linear correlation was found with the increment in energy consumption but not with the total energy consumption. This correlation was independent of the concentration of thrombin and indicated that complete secretion from dense, alpha- and acid-hydrolase-containing granules was paralleled by an increment of 4.0, 6.5 and 6.7 mumol of ATPeq. X (10(11) platelets)-1, respectively. An energy cost of 0.7 mumol of ATPeq. X (10(11) platelets)-1 was calculated for separate dense-granule secretion, whereas the combined alpha- and acid-hydrolase granule secretion required 5.3 mumol of ATPeq. X (10(11) platelets)-1. There was no correlation between energy consumption and optical aggregation. In contrast, the rate of single platelet disappearance, which is a measure for the early formation of small aggregates, correlated closely with the rate of energy consumption. Compared with secretion, however, the energy requirement of single platelet disappearance was minor, since 2mM-EDTA completely prevented this response but decreased the energy consumption only slightly. An increase of 0.5-1.0 mumol of ATPeq. X (10(11) platelets)-1 was seen before single platelet disappearance and the three secretion responses were initiated, indicating an increase in energy consuming processes that preceded these responses.(ABSTRACT TRUNCATED AT 400 WORDS)
通过测量致密颗粒、α颗粒和含酸水解酶颗粒聚集和分泌过程中的能量消耗,研究了代谢能量在血小板反应中的作用。用不同量的凝血酶(0.05 - 5.0单位×ml⁻¹)刺激凝胶过滤的人血小板。在聚集和分泌的不同阶段,通过ATP再合成突然停止后代谢ATP和ADP的变化来测量能量消耗。用5单位凝血酶×ml⁻¹刺激时,在最初15秒内能量消耗从6.2±0.9增加到17.8±0.4μmol ATPeq×min⁻¹×(10¹¹血小板)⁻¹。此后能量消耗下降,约30秒后恢复到静息细胞中的值。用0.05单位凝血酶×ml⁻¹刺激时,能量消耗加速较慢,至少3分钟后才恢复正常。在三个分泌反应的速度与同时的能量消耗之间发现了强正相关:(a)在给定剂量凝血酶诱导的反应的不同阶段,以及(b)在不同量凝血酶引发的不同分泌速度下。在反应的不同阶段,当将分泌程度与消耗的能量量进行比较时,发现与能量消耗的增加有强线性相关,但与总能量消耗无关。这种相关性与凝血酶浓度无关,表明致密颗粒、α颗粒和含酸水解酶颗粒完全分泌时,ATPeq分别增加4.0、6.5和6.7μmol×(10¹¹血小板)⁻¹。计算得出单独致密颗粒分泌的能量成本为0.7μmol ATPeq×(10¹¹血小板)⁻¹,而α颗粒和酸水解酶颗粒联合分泌需要5.3μmol ATPeq×(10¹¹血小板)⁻¹。能量消耗与光学聚集之间没有相关性。相反,单个血小板消失率(早期小聚集体形成的一种度量)与能量消耗率密切相关。然而,与分泌相比,单个血小板消失的能量需求较小,因为2mM - EDTA完全阻止了这种反应,但仅略微降低了能量消耗。在单个血小板消失和三个分泌反应开始之前,观察到ATPeq增加0.5 - 1.0μmol×(10¹¹血小板)⁻¹,表明在这些反应之前能量消耗过程增加。(摘要截断于400字)