Role of external Na+ and cytosolic pH in agonist-evoked cytosolic Ca2+ response in human platelets

Am J Physiol. 1994 Dec;267(6 Pt 1):C1543-52. doi: 10.1152/ajpcell.1994.267.6.C1543.

Abstract

The role of external Na+ in agonist-evoked platelet Ca2+ response is poorly understood. This was explored in this study. Removal of external Na+ decreased both cytosolic Ca2+ mobilization and external Ca2+ entry, induced by thrombin but not by ADP or vasopressin. That external Na+ regulates thrombin activities was demonstrated by 1) Na+ dependency of the amidolytic activity of thrombin, 2) inhibition of thrombin binding to the high-affinity binding sites in Na(+)-free medium, and 3) attenuation of thrombin-induced inositol 1,4,5-trisphosphate production in Na(+)-free medium. Moreover, Ca2+ response to the thrombin receptor 6-amino acid peptide was independent of external Na+. The role of external Na+ in modifying agonist-evoked Ca2+ response through activation of Na+/H+ antiport and cytosolic alkalinization was then explored. Cytosolic alkalinization by monensin or NH4Cl enhanced thrombin, ADP, and thimerosal-induced external Ca2+ entry. Thimerosal-induced acceleration of external Ca2+ entry was diminished by the inhibition of Na+/H+ antiport. Thus external Na+ enhances thrombin activities, and cytosolic pH mediates store-regulated external Ca2+ entry. However, Na+/H+ antiport activation is not essential for agonist-evoked Ca2+ mobilization and external Ca2+ entry.

Publication types

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

MeSH terms

  • Blood Platelets / metabolism*
  • Calcium / metabolism*
  • Cytosol / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Manganese / metabolism
  • Sodium / physiology*
  • Sodium-Hydrogen Exchangers / physiology
  • Thrombin / pharmacology*

Substances

  • Sodium-Hydrogen Exchangers
  • Manganese
  • Sodium
  • Thrombin
  • Calcium