Reversible and irreversible intracellular Ca2+ spiking in single isolated human platelets

被引:19
作者
Hussain, JF [1 ]
Mahaut-Smith, MP [1 ]
机构
[1] Univ Cambridge, Dept Physiol, Cambridge CB2 3EG, England
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1999年 / 514卷 / 03期
关键词
D O I
10.1111/j.1469-7793.1999.713ad.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. We have developed conditions that permit long duration recordings of [Ca2+](i) in single, isolated human platelets and studied the reversibility of Ca-i(2+) spiking following activation by physiological and artificial stimuli. 2. Fura-8-loaded platelets were immobilized at the tip of a saline-filled glass pipette using gentle suction. 'Contact' activation of Ca-i(2+) spiking was observed in a proportion (11 %) of platelets, which continued for the duration of each recording (range 8-45 min). 3. Platelets that displayed constant, resting Ca-i(2+) levels were used to test the effects of agonists. ADP (10 mu M) increased [Ca2+](i) in the form of either one to two spikes followed by an elevated plateau level (60 % of cells) or multiple Ca2+ spikes of irregular amplitude (40 % of cells). ADP-induced Ca-i(2+) mobilization was completely reversible and repeatable. 4. Thrombin (1 u ml(-1)) evoked Ca-i(2+) spiking in the majority (88 %) of platelets tested, which was not inhibited by perfusion of agonist-free saline throughout the recording period (range 8-67 min). 5. The clear difference in the reversibility of activation by different stimuli may reflect the distinct roles of individual agonists in haemostasis and have important consequences in the design of treatments for thrombosis.
引用
收藏
页码:713 / 718
页数:6
相关论文
共 30 条
[1]   SPATIAL-DISTRIBUTION AND TEMPORAL CHANGE IN CYTOSOLIC PH AND [CA2+] IN RESTING AND ACTIVATED SINGLE HUMAN PLATELETS [J].
ARIYOSHI, H ;
SALZMAN, EW .
CELL CALCIUM, 1995, 17 (05) :317-326
[2]   PLATELET PROCOAGULANT ACTIVITY - PHYSIOLOGICAL SIGNIFICANCE AND MECHANISMS OF EXPOSURE [J].
BEVERS, EM ;
COMFURIUS, P ;
ZWAAL, RFA .
BLOOD REVIEWS, 1991, 5 (03) :146-154
[3]   AGGREGATION OF BLOOD PLATELETS BY ADENOSINE DIPHOSPHATE AND ITS REVERSAL [J].
BORN, GVR .
NATURE, 1962, 194 (4832) :927-&
[4]   Thrombin receptor antagonists: A work in progress [J].
Brass, LF .
CORONARY ARTERY DISEASE, 1997, 8 (01) :49-58
[5]   Molecular basis for ADP-induced platelet activation I. Evidence for three distinct ADP receptors on human platelets [J].
Daniel, JL ;
Dangelmaier, C ;
Jin, JG ;
Ashby, B ;
Smith, JB ;
Kunapuli, SP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) :2024-2029
[6]   IGG-INDUCED CA2+ OSCILLATIONS IN DIFFERENTIATED U937 CELLS - A STUDY USING LASER-SCANNING CONFOCAL MICROSCOPY AND CO-LOADED FLUO-3 AND FURA-RED FLUORESCENT-PROBES [J].
FLOTO, RA ;
MAHAUTSMITH, MP ;
SOMASUNDARAM, B ;
ALLEN, JM .
CELL CALCIUM, 1995, 18 (05) :377-389
[7]  
HALLAM TJ, 1986, J PHYSIOL-LONDON, V377, pP123
[8]  
HEEMSKERK JWM, 1993, J BIOL CHEM, V268, P356
[9]   The Ca2+-mobilizing potency of alpha-thrombin and thrombin-receptor-activating peptide on human platelets - Concentration and time effects of thrombin-induced Ca2+ signaling [J].
Heemskerk, JWM ;
Feijge, MAH ;
Henneman, L ;
Rosing, J ;
Hemker, HC .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 249 (02) :547-555
[10]   SPIKING IN CYTOSOLIC CALCIUM-CONCENTRATION IN SINGLE FIBRINOGEN-BOUND FURA-2-LOADED HUMAN PLATELETS [J].
HEEMSKERK, JWM ;
HOYLAND, J ;
MASON, WT ;
SAGE, SO .
BIOCHEMICAL JOURNAL, 1992, 283 :379-383