NA-CA2+ EXCHANGE MODULATES CA2+ HANDLING OF HUMAN PLATELETS BY ALTERING INTRACELLULAR CA2+ STORE SIZE()

Citation
T. Ishida et al., NA-CA2+ EXCHANGE MODULATES CA2+ HANDLING OF HUMAN PLATELETS BY ALTERING INTRACELLULAR CA2+ STORE SIZE(), Journal of hypertension, 11(10), 1993, pp. 1089-1095
Citations number
32
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
02636352
Volume
11
Issue
10
Year of publication
1993
Pages
1089 - 1095
Database
ISI
SICI code
0263-6352(1993)11:10<1089:NEMCHO>2.0.ZU;2-1
Abstract
Objective: In order to elucidate the role of Na+-Ca2+ exchange in regu lating cytosolic free Ca2+ concentration in human platelets, we invest igated the relationship between cytosolic free Na+ and Ca2+ concentrat ions in human platelets.Methods: Sodium-binding benzofuran isophthalat e and fura-2 were used to monitor cytosolic free Na+ and Ca2+ concentr ations, respectively. Results: Ouabain at a concentration of 100 mumol /l induced an increase in cytosolic free Na+ concentration within 5 mi n, followed by increases in resting cytosolic free Ca2+ concentration and intracellular Ca2+ store. These three parameters were increased in a time-dependent manner significantly above the timed control over a period of 60 min. Pre-incubation of platelets with 100 mumol/l ouabain for 30 min significantly enhanced the cytosolic free Ca2+ response to thrombin and arginine vasopressin in the absence of extracellular Ca2 +. The decrease from peak cytosolic free Ca2+ concentration in respons e to ionomycin in the absence of extracellular Ca2+ was significantly slower in low-Na+ buffer than in standard buffer. In addition, 5 mumol /l ionomycin increased the cytosolic free Na+ concentration markedly i n the presence of 0.1 mmol/l extracellular Ca2+, but the rise in cytos olic free Na+ concentration was suppressed by 2 mmol/l Ni2+ (NiCl2) or by removal of extracellular Ca2+. Conclusions. These results suggest that Na+-Ca2+ exchange is important in extruding Ca2+ from the cytosol in human platelets, and inhibition of this exchange leads to the accu mulation of intracellular Ca2+ store, which may be responsible for the enhanced responsiveness of cytosolic free Ca2+ to agonists.