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Research Article Free access | 10.1172/JCI107336

Identification of Inorganic Pyrophosphate in Human Platelets and Its Release on Stimulation with Thrombin

Donald C. Silcox, Sergio Jacobelli, and Daniel J. McCarty

Section of Arthritis and Metabolism, Department of Medicine, University of Chicago Pritzker School of Medicine, Chicago, Illinois 60637

Find articles by Silcox, D. in: PubMed | Google Scholar

Section of Arthritis and Metabolism, Department of Medicine, University of Chicago Pritzker School of Medicine, Chicago, Illinois 60637

Find articles by Jacobelli, S. in: PubMed | Google Scholar

Section of Arthritis and Metabolism, Department of Medicine, University of Chicago Pritzker School of Medicine, Chicago, Illinois 60637

Find articles by McCarty, D. in: PubMed | Google Scholar

Published July 1, 1973 - More info

Published in Volume 52, Issue 7 on July 1, 1973
J Clin Invest. 1973;52(7):1595–1600. https://doi.org/10.1172/JCI107336.
© 1973 The American Society for Clinical Investigation
Published July 1, 1973 - Version history
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Abstract

Serum inorganic pyrophosphate (PPi) levels were consistently two- to threefold higher than plasma PPi prepared from the same blood. PPi was found in platelets in amounts ranging from 1.4 to 3 nmol/108 cells, using three different techniques for quantification. These levels are approximately 800 times higher than the mean PPi concentration in normal plasma and approximate the levels of ADP found in platelets by other workers.

About 50% of platelet PPi was specifically released extracellularly after stimulation with thrombin. Timed release experiments showed a pattern of release that resembled that described for ADP and ATP. This pattern was clearly different from that shown by platelet calcium, serotonin, or β-glucuronidase. Platelet inorganic pyrophosphatase was not released into the supernate in detectable amounts.

Platelets from patients with nucleotide storage pool deficiency showed greatly reduced levels of PPi as compared with control. There was no detectable release of PPi into extracellular medium after thrombin addition to a suspension of these platelets.

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