The contributions of plasma membrane Na+-Ca2+-exchange and the Ca2+-ATPase to the regulation of cytosolic calcium ([Ca2+]i) in a clonal pituitary cell line (AtT-20) of mouse corticotropes

Life Sci. 2001 Dec 28;70(6):681-98. doi: 10.1016/s0024-3205(01)01443-6.

Abstract

Single cell calcium microfluorimetry was used to examine the regulation of [Ca2+]i homeostasis in a clonal cell line of corticotropes (AtT-20 cells). Single cells, loaded with fura-2/AM, were exposed briefly to elevated potassium chloride (KCI, 40 mM, 5 sec). The time constant of decay of the [Ca2+]i signal was used as an index of [Ca2+]i extrusion and/or sequestration. Substitution of extracellular sodium with lithium, N-methyl-D-glucamine (NMDG), or Tris, increased resting levels of [Ca2+]i and significantly increased the time constant of [Ca2+]i decay by 40% compared to control indicating the participation of Na+-Ca2+-exchange. Prior exposure of single cells to thapsigargin (1 microM) or BuBHQ (10 microM). inhibitors of the SERCA Ca2+-ATPases, and/or the mitochondrial uncoupler FCCP (1 microM) did not significantly change the time constant of [Ca2+]i decay following KCl. Lanthanum ions (La3+), applied during the decay of the KCI-induced increase in [Ca2+]i, significantly increased the time constant of the return of [Ca2+]i to resting levels by 70% compared to control. Brief exposure of cells to sodium orthovanadate, an inhibitor of ATP-dependent pump activity, slowed and longer exposures prevented, the return of [Ca2+]i to resting levels. We conclude that neither intracellular SERCA pumps nor mitochondrial uptake contribute significantly to [Ca2+]i sequestration following a [Ca2+]i load and that the plasma membrane Ca2+-ATPase contributes to a greater extent than the Na+-Ca2+-exchanger to the return of [Ca2+]i to resting levels following a [Ca2+]i load under these experimental conditions.

MeSH terms

  • Animals
  • Calcium-Transporting ATPases / antagonists & inhibitors
  • Calcium-Transporting ATPases / metabolism*
  • Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone / pharmacology
  • Cell Line
  • Cell Membrane / enzymology*
  • Clone Cells
  • Enzyme Inhibitors / pharmacology
  • Fura-2 / pharmacology
  • Hydroquinones / pharmacology
  • Image Processing, Computer-Assisted
  • Ionomycin / pharmacology
  • Lithium / pharmacology
  • Meglumine / pharmacology
  • Meglumine Antimoniate
  • Mice
  • Organometallic Compounds / pharmacology
  • Organophosphates / pharmacology
  • Pituitary Gland / cytology
  • Pituitary Gland / drug effects
  • Pituitary Gland / enzymology*
  • Potassium Chloride / pharmacology
  • Signal Transduction
  • Sodium-Calcium Exchanger / antagonists & inhibitors
  • Sodium-Calcium Exchanger / metabolism*
  • Tetraethylammonium / pharmacology
  • Thapsigargin / pharmacology

Substances

  • Enzyme Inhibitors
  • Hydroquinones
  • Organometallic Compounds
  • Organophosphates
  • Sodium-Calcium Exchanger
  • tris(2,3-dibromopropyl)phosphate
  • 2,5-di-tert-butylhydroquinone
  • Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
  • Ionomycin
  • Tetraethylammonium
  • Potassium Chloride
  • Thapsigargin
  • Meglumine
  • Meglumine Antimoniate
  • Lithium
  • Calcium-Transporting ATPases
  • Fura-2