Lysophospholipids regulate excitability and exocytosis in cultured bovine chromaffin cells

J Neurochem. 2007 Aug;102(3):944-56. doi: 10.1111/j.1471-4159.2007.04584.x.

Abstract

Bioactive lysophospholipids (LPLs) are released by blood cells and can modulate many cellular activities such as angiogenesis and cell survival. In this study, the effects of sphingosine-1-phosphate (S1P) and lysophosphatidic acid (LPA) on excitability and exocytosis in bovine chromaffin cells were investigated using the whole-cell configuration of the patch-clamp. Voltage-gated Ca(2+) current was inhibited by S1P and LPA pre-treatment in a concentration-dependent manner with IC(50)s of 0.46 and 0.79 mumol/L, respectively. Inhibition was mostly reversible upon washout and prevented by suramin, an inhibitor of G-protein signaling. Na(+) current was inhibited by S1P, but not by LPA. However, recovery of Na(+) channels from inactivation was slowed by both LPLs. The outward K(+) current was also significantly reduced by both LPLs. Chromaffin cells fired repetitive action potentials in response to minimal injections of depolarizing current. Repetitive activity was dramatically reduced by LPLs. Consistent with the reduction in Ca(2+) current, exocytosis elicited by a train of depolarizations and the ensuing endocytosis were both inhibited by LPL pre-treatments. These data demonstrate the interaction between immune and endocrine systems mediated by the inhibitory effects of LPLs on the excitability of adrenal chromaffin cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Adrenal Medulla / metabolism*
  • Adrenal Medulla / ultrastructure
  • Animals
  • Cattle
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism*
  • Cells, Cultured
  • Chromaffin Cells / drug effects
  • Chromaffin Cells / metabolism*
  • Dose-Response Relationship, Drug
  • Electric Stimulation
  • Endocytosis / drug effects
  • Endocytosis / physiology
  • Exocytosis / drug effects
  • Exocytosis / physiology
  • Immunologic Factors / metabolism
  • Immunologic Factors / pharmacology
  • Lysophospholipids / metabolism*
  • Lysophospholipids / pharmacology
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Neurosecretory Systems / drug effects
  • Neurosecretory Systems / metabolism
  • Patch-Clamp Techniques
  • Potassium Channels / drug effects
  • Potassium Channels / metabolism
  • Receptors, G-Protein-Coupled / drug effects
  • Receptors, G-Protein-Coupled / metabolism
  • Sodium Channels / drug effects
  • Sodium Channels / metabolism
  • Sphingosine / analogs & derivatives
  • Sphingosine / metabolism
  • Sphingosine / pharmacology
  • Suramin / pharmacology

Substances

  • Immunologic Factors
  • Lysophospholipids
  • Potassium Channels
  • Receptors, G-Protein-Coupled
  • Sodium Channels
  • sphingosine 1-phosphate
  • Suramin
  • Sphingosine
  • lysophosphatidic acid