Cell shrinkage is essential in lysophosphatidic acid signaling in Ehrlich ascites tumor cells

J Membr Biol. 2000 Jan 1;173(1):19-29. doi: 10.1007/s002320001003.

Abstract

The present study aimed at elucidating the initial intracellular lysophosphatidic acid (LPA)-induced signaling events, in order to investigate the sequence in which LPA affects the intracellular concentration of free, cytosolic Ca(2+), [Ca(2+)](i), ion channels, the F-actin cytoskeleton, cell volume and the Na(+)/H(+) exchanger. We found that stimulation of Ehrlich cells with LPA induced a transient, concentration-dependent increase in [Ca(2+)](i), which is due to Ca(2+) release from intracellular Ins(1,4,5)P(3)-sensitive stores as well as an influx of Ca(2+). The EC(50) values for LPA-induced Ca(2+) mobilization were estimated at 0.03 nm and 0.4 nm LPA in the presence and absence of extracellular Ca(2+), respectively. The LPA-induced increase in [Ca(2+)](i) resulted in (i) co-activation of Ca(2+)-activated, charybdotoxin (ChTX)-sensitive K(+) and niflumic acid-sensitive Cl(-) currents; (ii) a subsequent cell shrinkage and increased polymerization of F-actin, and (iii) activation of a Na(+)/H(+) exchange, resulting in a concentration-dependent intracellular alkalinization. The EC(50) value for the LPA-induced rate of alkalinization was estimated at 0. 37 nm LPA. When cell shrinkage was prevented, the LPA-induced activation of the Na(+)/H(+) exchanger was impaired. In conclusion, the initial signaling events induced by LPA involves activation of volume regulatory mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / drug effects
  • Animals
  • Calcium / metabolism*
  • Carcinoma, Ehrlich Tumor / pathology
  • Carcinoma, Ehrlich Tumor / physiopathology*
  • Cell Membrane / drug effects
  • Cell Membrane / physiology
  • Cell Size / drug effects
  • Charybdotoxin / pharmacology
  • Chloride Channels / physiology
  • Chlorides / metabolism
  • Cytoskeleton / drug effects
  • Cytosol / metabolism
  • Female
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Lysophospholipids / pharmacology*
  • Membrane Potentials / physiology
  • Mice
  • Mice, Inbred Strains
  • Niflumic Acid / pharmacology
  • Potassium / metabolism
  • Rubidium / pharmacokinetics
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Sodium-Hydrogen Exchangers / drug effects
  • Sodium-Hydrogen Exchangers / metabolism
  • Taurine / metabolism
  • Tumor Cells, Cultured

Substances

  • Actins
  • Chloride Channels
  • Chlorides
  • Lysophospholipids
  • Sodium-Hydrogen Exchangers
  • Charybdotoxin
  • Taurine
  • Niflumic Acid
  • Inositol 1,4,5-Trisphosphate
  • Rubidium
  • Potassium
  • Calcium