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pubmed-article:7626597pubmed:abstractTextPlatelet accretion at sites of vascular injury yields a neo-tissue comprising packed platelets and having an interstitial space not supplied with blood. Within growing thrombi platelet masses become anoxic and depolarize to yield interstitial cation concentrations characteristic of the more voluminous platelet cytosol, with extracellular [Ca2+] falling below that adequate to support the plasma clotting system. The platelet-associated clotting system reactivates during disaggregation of the thrombi in vitro, which proceeds with high yield of apparently basal, functional platelets when specific anticoagulants are included in the disaggregating media. The capacity of regulatory demand to lower extracellular [Ca2+] in the microenvironment of platelet aggregates provides a physiological basis for evolution of the highly cooperative calcium interactions of the hemostasis system.lld:pubmed
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pubmed-article:7626597pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:7626597pubmed:articleTitleGating of thrombin in platelet aggregates by pO2-linked lowering of extracellular Ca2+ concentration.lld:pubmed
pubmed-article:7626597pubmed:affiliationDepartment of Biochemistry and Molecular Biology, Mayo Foundation for Education and Research, Rochester, Minnesota 55905, USA.lld:pubmed
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pubmed-article:7626597pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:7626597pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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