Preparation of Suspensions of Washed Platelets from Humans

Authors

  • J. F. Mustard,

    Corresponding author
    1. Department of Pathology, McMaster University, Hamilton, Ontario, and Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada
      Dr J. F. Mustard, Department of Pathology, McMaster University, Hamilton, Ontario, Canada.
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  • D. W. Perry,

    1. Department of Pathology, McMaster University, Hamilton, Ontario, and Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada
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  • N. G. Ardlie,

    1. Department of Pathology, McMaster University, Hamilton, Ontario, and Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada
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  • M. A. Packham

    1. Department of Pathology, McMaster University, Hamilton, Ontario, and Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada
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Dr J. F. Mustard, Department of Pathology, McMaster University, Hamilton, Ontario, Canada.

Abstract

Summary: Methods have been developed for the preparation of suspensions of washed platelets from humans. Heparin is used in the washing fluids to prevent: thrombin generation and apyrase is used to prevent adenine nucleotide accumulation. Platelets suspended in Eagle's tissue culture medium containing albumin were more responsive to ADP than platelets in Tyrode's-albumin solution. Addition of fibrinogen is required for maximum sensitivity to ADP-induced aggregation. These platelets can be stored for 4 hr or more at 37°C in the presence of apyrase and maintain their ability to aggregate upon the addition of low concentrations of ADP.

Without apyrase the platelets gradually become insensitive to ADP upon storage at 37°C; this is presumably caused by the accumulation of ADP in the suspending fluid because sensitivity can be partially restored by the addition of apyrase and further incubation.

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