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. 1973 Apr;61(4):462-81.
doi: 10.1085/jgp.61.4.462.

Calcium uptake and associated adenosine triphosphatase activity of isolated platelet membranes

Calcium uptake and associated adenosine triphosphatase activity of isolated platelet membranes

L S Robblee et al. J Gen Physiol. 1973 Apr.

Abstract

A platelet subcellular fraction, sedimenting between 14,000 and 40,000 g and consisting primarily of membrane vesicles, accumulates up to 200-400 nmoles calcium/mg protein in the presence of ATP and oxalate. Steady-state levels of calcium accumulation are attained in 40-60 min. Calcium uptake requires adenosine triphosphate (ATP), is enhanced by oxalate, and is accompanied by the release of inorganic phosphate. Calcium accumulation and phosphate release require magnesium and are inhibited by Salyrgan (10 microM) and adenosine diphosphate (ADP) (1 mM), but not by ouabain (0.1 mM). The ATPase activity is stimulated by low concentrations of calcium (5-10 microM) and is inhibited by 2 mM EGTA. Electron microscopic histochemistry using lead nitrate to precipitate released phosphate results in lead precipitates localized primarily at the inner surface of membrane vesicles. These results provide evidence for a membrane ATPase that is stimulated by low concentrations of calcium and may be involved in the transport of calcium across the membrane. It is postulated that the observed calcium uptake activity is an in vitro manifestation of a calcium extrusion pump in the intact platelet.

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References

    1. J Biophys Biochem Cytol. 1961 Feb;9:409-14 - PubMed
    1. Bull Soc Chim Biol (Paris). 1958;40(11):1623-36 - PubMed
    1. Science. 1970 Apr 10;168(3928):255-7 - PubMed
    1. J Gen Physiol. 1971 Feb;57(2):202-15 - PubMed
    1. J Gen Physiol. 1967 May;50(5):1327-52 - PubMed

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