Alpha-granule secretion from alpha-toxin permeabilized, MgATP-exposed platelets is induced independently by H+ and Ca2+

J Cell Physiol. 1999 Apr;179(1):1-10. doi: 10.1002/(SICI)1097-4652(199904)179:1<1::AID-JCP1>3.0.CO;2-E.

Abstract

In order to better understand granule release from platelets, we developed an alpha-toxin permeabilized platelet model to study alpha-granule secretion. Secretion of alpha-granules was analyzed by flow cytometry using P-selectin as a marker for alpha-granule release. P-selectin surface expression occurred when platelets were permeabilized in the presence of Ca2+. Responsiveness to Ca2+ was lost 30 min after permeabilization but could be reconstituted with MgATP. Alpha-toxin-permeabilized, MgATP-exposed platelets also degranulated within a pH range of 5.4-5.9 without exposure to and independent of Ca2+. ATP, GTP, CTP, UTP, and ITP supported Ca2+-induced alpha-granule secretion, while H+-induced alpha-granule secretion occurred only with ATP and GTP. Both Ca2+- and H+-induced alpha-granule secretion required ATP hydrolysis. Kinase inhibitors blocked both Ca2+- and H+-induced secretion. These data suggest that alpha-granule secretion in this permeabilized platelet system shares many characteristics with granule secretion studied in other permeabilized cell models. Furthermore, these results show that H+ can trigger alpha-granule release independent of Ca2+.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / pharmacology*
  • Blood Platelets / drug effects*
  • Blood Platelets / metabolism
  • Calcium / pharmacology*
  • Cell Membrane Permeability / drug effects
  • Cytoplasmic Granules / metabolism*
  • Egtazic Acid / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Flow Cytometry
  • Genistein / pharmacology
  • Guanosine Triphosphate / pharmacology
  • Humans
  • Hydrogen-Ion Concentration
  • Isoquinolines / pharmacology
  • Magnesium / pharmacology*
  • Manganese / pharmacology
  • Nucleotides / pharmacology
  • P-Selectin / analysis
  • Protein Kinase Inhibitors
  • Protons*
  • Staurosporine / pharmacology
  • Sulfonamides*
  • Type C Phospholipases / pharmacology*
  • Tyrphostins / pharmacology
  • beta-Thromboglobulin / metabolism

Substances

  • Enzyme Inhibitors
  • Isoquinolines
  • Nucleotides
  • P-Selectin
  • Protein Kinase Inhibitors
  • Protons
  • Sulfonamides
  • Tyrphostins
  • beta-Thromboglobulin
  • Manganese
  • Egtazic Acid
  • Guanosine Triphosphate
  • Adenosine Triphosphate
  • Genistein
  • Type C Phospholipases
  • Staurosporine
  • Magnesium
  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide
  • Calcium