Literature DB >> 1469706

Rapid Ca2+ extrusion via the Na+/Ca2+ exchanger of the human platelet.

P A Valant1, P N Adjei, D H Haynes.   

Abstract

This communication reports the kinetics of the Na+/Ca2+ exchanger and of the plasma membrane (PM) Ca2+ pump of the intact human platelet. The kinetic properties of these two systems were deduced by studying the rate of Ca2+ extrusion and its Na+ dependence for concentrations of cytoplasmic free Ca2+ ([Ca2+]cyt) in the 1-10-microM range. The PM Ca(2+)-ATPase was previously characterized (Johansson, J.S. Haynes, D.H. 1988. J. Membrane Biol. 104:147-163) for [Ca2+]cyt < or = 1.5 microM with the fluorescent Ca2+ indicator quin2 (Kd = 115 nM). That study determined that the PM Ca2+ pump in the basal state has a Vmax = 0.098 mM/min, a Km = 80 nM and a Hill coefficient = 1.7. The present study extends the measurable range of [Ca2+]cyt with the intracellular Ca2+ probe, rhod2 (Kd = 500 nM), which has almost a fivefold lower affinity for Ca2+. An Appendix also describes the Mg2+ and pH dependence of the Kd and fluorescence characteristics of the commercially available dye, which is a mixture of two molecules. Rates of active Ca2+ extrusion were determined by two independent methods which gave good agreement: (i) by measuring Ca2+ extrusion into a Ca(2+)-free medium (above citation) or (ii) by the newly developed "ionomycin short-circuit" method, which determines the ionomycin concentration necessary to short circuit the PM Ca2+ extrusion systems. Absolute rates of extrusion were determined by knowledge of how many Ca2+ ions are moved by ionomycin per minute. The major findings are as follows: (i) The exchanger is saturable with respect to Ca2+ with a Km = 0.97 +/- 0.31 microM and Vmax = 1.0 +/- 0.6 mM/min. (ii) At high [Ca2+]cyt, the exchanger works at a rate 10 times as large as the basal Vmax of the PM Ca2+ extrusion pump. (iii) The exchanger can work in reverse after Na+ loading of the cytoplasm by monensin. (iv) The PM Ca2+ extrusion pump is activated by exposure to [Ca2+]cyt > or = 1.5 microM for 20-50 sec. Activation raises the pump Vmax to 1.6 +/- 0.6 mM/min and the Km to 0.55 +/- 0.24 microM. (v) The Ca2+ buffering capacity of the cytoplasm is 3.6 mM in the 0.1 to 3 microM range of [Ca2+]cyt. In summary, the results show that the human platelet can extrude Ca2+ very rapidly at high [Ca2+]cyt. Both the Na+/Ca2+ exchanger and Ca2+ pump activation may prevent inappropriate platelet activation by marginal stimuli.

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Year:  1992        PMID: 1469706     DOI: 10.1007/bf00233739

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  31 in total

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Authors:  A Fabiato
Journal:  J Gen Physiol       Date:  1985-02       Impact factor: 4.086

2.  Platelet free calcium concentrations measured with fura-2 are influenced by the transmembrane sodium gradient.

Authors:  J Schaeffer; M P Blaustein
Journal:  Cell Calcium       Date:  1989 Feb-Mar       Impact factor: 6.817

3.  Role of Na+/H+ exchange in thrombin- and arachidonic acid-induced Ca2+ influx in platelets.

Authors:  D Ghigo; S Treves; F Turrini; A Pannocchia; G Pescarmona; A Bosia
Journal:  Biochim Biophys Acta       Date:  1988-05-09

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Authors:  M P Mahaut-Smith; S O Sage; T J Rink
Journal:  J Biol Chem       Date:  1990-06-25       Impact factor: 5.157

5.  Activation of Na+/H+ exchange and Ca2+ mobilization start simultaneously in thrombin-stimulated platelets. Evidence that platelet shape change disturbs early rises of BCECF fluorescence which causes an underestimation of actual cytosolic alkalinization.

Authors:  W Siffert; G Siffert; P Scheid; J W Akkerman
Journal:  Biochem J       Date:  1989-03-01       Impact factor: 3.857

6.  Cytoplasmic Mg2+ concentration in platelets: implications for determination of Ca2+ with aequorin.

Authors:  J A Ware; M Smith; E T Fossel; E W Salzman
Journal:  Am J Physiol       Date:  1988-10

7.  Calcium homeostasis in intact lymphocytes: cytoplasmic free calcium monitored with a new, intracellularly trapped fluorescent indicator.

Authors:  R Y Tsien; T Pozzan; T J Rink
Journal:  J Cell Biol       Date:  1982-08       Impact factor: 10.539

8.  Cyclic AMP stimulates Ca(2+)-ATPase-mediated Ca2+ extrusion from human platelets.

Authors:  J S Johansson; L E Nied; D H Haynes
Journal:  Biochim Biophys Acta       Date:  1992-03-23

9.  Cyclic GMP increases the rate of the calcium extrusion pump in intact human platelets but has no direct effect on the dense tubular calcium accumulation system.

Authors:  J S Johansson; D H Haynes
Journal:  Biochim Biophys Acta       Date:  1992-03-23

10.  Myoplasmic free calcium concentration reached during the twitch of an intact isolated cardiac cell and during calcium-induced release of calcium from the sarcoplasmic reticulum of a skinned cardiac cell from the adult rat or rabbit ventricle.

Authors:  A Fabiato
Journal:  J Gen Physiol       Date:  1981-11       Impact factor: 4.086

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Authors:  Y X Li; J Rinzel; J Keizer; S S Stojilković
Journal:  Proc Natl Acad Sci U S A       Date:  1994-01-04       Impact factor: 11.205

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4.  A positive feedback cell signaling nucleation model of astrocyte dynamics.

Authors:  Christopher L Macdonald; Gabriel A Silva
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  4 in total

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