Ca(2+) and Na(+) contribute to the swelling of differentiated neuroblastoma cells induced by equinatoxin-II

Toxicon. 2000 Nov;38(11):1547-60. doi: 10.1016/s0041-0101(00)00088-x.

Abstract

Equinatoxin-II (EqTx-II), a cytotoxic protein (mol.wt 20 kDa) isolated from the sea anemone Actinia equina, was found to consistently increase the three-dimensional projected area of differentiated neuroblastoma (NG108-15) cells provided Ca(2+) was present in the medium. No swelling was detected when external NaCl was replaced by sucrose, but replacement of NaCl by Na-isethionate did not prevent the swelling, as revealed by confocal laser scanning microscopy. In addition, microspectrofluorometric measurements in cells preloaded with the Ca(2+) indicator fura-2/AM revealed that EqTx-II (100 nM) markedly increased the fluorescence (F(340)/F(380)) ratio indicating a rise of intracellular Ca(2+) concentration ([Ca(2+)](i)). The elevation of [Ca(2+)](i) exhibited two components that seem to be related to the kinetics of EqTx-II-induced Ca(2+) entry since pretreatment of cells with Ca(2+)-ATPase inhibitors (thapsigargin), Ca(2+) channel blockers (nifedipine and Gd(3+)) or prolonged exposure to a high K(+) (75 mM) medium did not alter EqTx-II-induced Ca(2+) signals. As far as we know, this is the first demonstration that EqTx-II causes swelling of neuroblastoma cells and that this effect is correlated both with an increase of [Ca(2+)](i) and needs the presence of extracellular Na(+). It is suggested that EqTx-II has the ability to insert into the plasma membrane of neuroblastoma cells and to form pores altering the membrane permeability and the intracellular osmolality, inducing a marked influx of water into the cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium Channel Blockers / pharmacology
  • Calcium Signaling / drug effects
  • Calcium-Transporting ATPases / antagonists & inhibitors
  • Cell Differentiation
  • Cnidarian Venoms / toxicity*
  • Cytotoxins / toxicity*
  • Enzyme Inhibitors / pharmacology
  • Membrane Potentials / drug effects
  • Mice
  • Microscopy, Confocal / methods
  • Neuroblastoma / pathology*
  • Rats
  • Sea Anemones / chemistry
  • Sodium / metabolism*
  • Tumor Cells, Cultured

Substances

  • Calcium Channel Blockers
  • Cnidarian Venoms
  • Cytotoxins
  • Enzyme Inhibitors
  • equinatoxin
  • Sodium
  • Calcium-Transporting ATPases
  • Calcium