Modulation of calcium homeostasis in cultured rat aortic endothelial cells by intracellular acidification

Am J Physiol. 1993 Oct;265(4 Pt 2):H1424-33. doi: 10.1152/ajpheart.1993.265.4.H1424.

Abstract

Acidosis produces vasodilation in a process that may involve the vascular endothelium. Because synthesis and release of endothelium-derived vasodilatory substances are linked to an increase in cytosolic calcium concentration ([Ca2+]i), we examined the effect of intracellular acidification on cultured rat aortic endothelial cells loaded either with the pH-sensitive probe carboxy-seminaphthorhodafluor-1 or the Ca(2+)-sensitive fluorescent probe indo 1. The basal cytosolic pH (pHi) of endothelial monolayers in a 5% CO2-HCO3- buffer was 7.27 +/- 0.02 and that in a bicarbonate-free solution was 7.22 +/- 0.03. Acidification was induced either by removal of NH4Cl (delta pHi = -0.10 +/- 0.02), changing from a bicarbonate-free to a 5% CO2-HCO3(-)-buffered solution at constant buffer pH (delta pHi = -0.18 +/- 0.03), or changing from a 5% to a 20% CO2-HCO3- solution (delta pHi = -0.27 +/- 0.07). Regardless of the method used, intracellular acidification increased [Ca2+]i as indexed by indo 1 fluorescence. The increase in [Ca2+]i induced by changing from a 5 to a 20% CO2-HCO3- solution was not significantly altered by removal of buffer Ca2+ either before or after depletion of bradykinin- and thapsigargin-sensitive intracellular Ca2+ stores. Thus intracellular acidification of vascular endothelial cells releases Ca2+ into the cytosol either from pH-sensitive intracellular buffer sites, mitochondria, or from bradykinin- and thapsigargin-insensitive intracellular stores. This Ca2+ mobilization may be linked to endothelial synthesis and release of vasodilatory substances during acidosis.

MeSH terms

  • Acids / metabolism*
  • Ammonium Chloride / pharmacology
  • Animals
  • Aorta / cytology
  • Aorta / metabolism*
  • Bicarbonates / pharmacology
  • Bradykinin / pharmacology
  • Buffers
  • Calcium / metabolism*
  • Calcium-Transporting ATPases / antagonists & inhibitors
  • Carbon Dioxide / pharmacology
  • Cells, Cultured
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism*
  • Homeostasis
  • Hydrogen-Ion Concentration
  • Intracellular Membranes / metabolism*
  • Rats
  • Rats, Wistar
  • Terpenes / pharmacology
  • Thapsigargin

Substances

  • Acids
  • Bicarbonates
  • Buffers
  • Terpenes
  • Ammonium Chloride
  • Carbon Dioxide
  • Thapsigargin
  • Calcium-Transporting ATPases
  • Bradykinin
  • Calcium