Agonist-evoked alkaline shift in the cytosolic pH set point for activation of Na+/H+ antiport in human platelets. The role of cytosolic Ca2+ and protein kinase C

J Biol Chem. 1990 Dec 5;265(34):21068-74.

Abstract

This work examines the roles of elevated cytosolic Ca2+ and stimulation of protein kinase C in agonist and non-agonist-mediated alkaline shift of the cytosolic pH set point for activation of Na+/H+ antiport in human platelets. Ca2(+)-depleted and control platelets were subjected to phorbol 12-myristate 13-acetate, thrombin, vasopressin, and ionomycin in 1 mM or Ca2+ free, nominally bicarbonate free media. To measure the cytosolic pH set point for Na+/H+ antiport activation, cells were acidified to different levels using the sodium propionate method. In some experiments protein kinase C was inhibited by staurosporine. Both protein kinase C stimulation and elevation of cytosolic Ca2+ can produce an alkaline shift in the pH set point for activation of Na+/H+ antiport in human platelets. However, the effect of Ca2+i on the pH set point predominates that of protein kinase C stimulation. Cytosolic Ca2+ is a prerequisite for agonist-evoked alkaline shift in the cytosolic pH set point for activation of Na+/H+ antiport. The cytosolic Ca2+ level is also essential for maintaining the basal cytosolic pH. These findings underscore the central role of cytosolic Ca2+ under basal and stimulated states in regulating cytosolic pH of human platelets.

Publication types

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

MeSH terms

  • Alkaloids / pharmacology
  • Blood Platelets / drug effects
  • Blood Platelets / metabolism*
  • Calcium / blood
  • Carrier Proteins / blood*
  • Humans
  • Hydrogen-Ion Concentration
  • Ionomycin / pharmacology
  • Kinetics
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / blood
  • Sodium-Hydrogen Exchangers
  • Staurosporine
  • Thrombin / pharmacology
  • Vasopressins / pharmacology

Substances

  • Alkaloids
  • Carrier Proteins
  • Sodium-Hydrogen Exchangers
  • Vasopressins
  • Ionomycin
  • Protein Kinase C
  • Thrombin
  • Staurosporine
  • Calcium