Thromb Haemost 1988; 59(01): 054-061
DOI: 10.1055/s-0038-1642565
Review Article
Schattauer GmbH Stuttgart

Identity of Saturable Calcium-Binding Sites on Blood Platelets and Their Involvement in Platelet Aggregation

Geoffrey I Johnston
The Department of Medicine, University Hospital, Queen’s Medical Centre, Nottingham, UK
*   Current address:, Dept. of Medicine/Cardiovascular Blology Research Program, Oklahoma University Health Science Center-line 825 Northeast 13th Street Oklahoma City, Oklahoma 73104, USA
,
Stanley Heptinstall
The Department of Medicine, University Hospital, Queen’s Medical Centre, Nottingham, UK
› Author Affiliations
Further Information

Publication History

Received 07 April 1987

Accepted after revision 02 October 1987

Publication Date:
18 April 2018 (online)

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Summary

Extracellular Ca2+ ions are required for platelet aggregation and we show that they enter two platelet pools. One pool is rapidly filled and easily displaced by EGTA. The second is filled more slowly and is not displaced by EGTA. The EGTA-displaceable pool is believed to be surface-located and was found to contain at least one class of saturable binding sites as well as a class of non-saturable binding sites. The saturable sites were found to be highly selective for Ca2+ (dissociation constant, 3.5 × IO−7 M) even in the presence of 1 mM Mg2+ ions, and they took up between 261,000 and 307,000 Ca2+ ions/platelet. Full occupancy of the saturable binding sites appeared to be necessary for platelet aggregation to proceed. We also studied platelets that were unable to aggregate normally, either due to the congenital bleeding disorder Glanzmann’s thrombastenia or due to experimental manipulation. In both cases wc found decreased Ca2+uptake specifically by the saturable Ca2+ binding sites, and that this was associated with decreased number of GP IIb/IIIa molecules expressed on these platelets. We suggest that the Ca2+binding sites involved in platelet aggregation are located on the GP Ilb/IIIa complexes and may be involved in holding the glycoproteins in the complex together, and that the binding sites need to be fully occupied before aggregation can proceed.