A store-operated Ca(2+) influx pathway in the bag cell neurons of Aplysia

J Neurophysiol. 2006 Nov;96(5):2688-98. doi: 10.1152/jn.00118.2006. Epub 2006 Aug 2.

Abstract

Although store-operated Ca(2+) influx has been well-studied in nonneuronal cells, an understanding of its nature in neurons remains poor. In the bag cell neurons of Aplysia californica, prior work has suggested that a Ca(2+) entry pathway can be activated by Ca(2+) store depletion. Using fura-based imaging of intracellular Ca(2+) in cultured bag cell neurons, we now characterize this pathway as store-operated Ca(2+) influx. In the absence of extracellular Ca(2+), the endoplasmic reticulum Ca(2+)-ATPase inhibitors, cyclopiazonic acid (CPA) or thapsigargin, depleted intracellular stores and elevated intracellular free Ca(2+). With the subsequent addition of extracellular Ca(2+), a prominent Ca(2+) influx was observed. The ryanodine receptor agonist, chloroethylphenol (CEP), also increased intracellular Ca(2+) but did not initiate store-operated Ca(2+) influx, despite overlap between CEP- and CPA-sensitive stores. Bafilomycin A, a vesicular H(+)-ATPase inhibitor, liberated intracellular Ca(2+) from acidic stores and attenuated subsequent Ca(2+) influx, presumably by replenishing CPA-depleted stores. Store-operated Ca(2+) influx was partially blocked by low concentrations of La(3+) or BTP2, and strongly inhibited by either 1-[b-[3-(4-methoxyphenyl)propoxy]-4-methoxyphenethyl]-1H-imidazole (SKF-96365) or a high concentration of Ni(2+). Regarding IP(3) receptor blockers, 2-aminoethyldiphenyl borate, but not xestospongin C, prevented store-operated Ca(2+) influx. However, jasplakinolide, an actin stabilizer reported to inhibit this pathway in smooth muscle cell lines, was ineffective. The bag cell neurons initiate reproductive behavior through a prolonged afterdischarge associated with intracellular Ca(2+) release and neuropeptide secretion. Store-operated Ca(2+) influx may serve to replenish stores depleted during the afterdischarge or participate in the release of peptide that triggers behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anilides / pharmacology
  • Animals
  • Aplysia / physiology*
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels / physiology*
  • Calcium Signaling / physiology*
  • Electrophysiology
  • Enzyme Inhibitors / pharmacology
  • Imidazoles / pharmacology
  • In Vitro Techniques
  • Indicators and Reagents
  • Indoles / pharmacology
  • Inositol 1,4,5-Trisphosphate / pharmacology
  • Lanthanum / pharmacology
  • Macrocyclic Compounds / pharmacology
  • Membrane Potentials / physiology
  • Neurons / physiology*
  • Nickel / pharmacology
  • Oxazoles / pharmacology
  • Ryanodine Receptor Calcium Release Channel / drug effects
  • Thapsigargin / pharmacology
  • Thiadiazoles / pharmacology

Substances

  • 4-methyl-4'-(3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl)-1,2,3-thiadiazole-5-carboxanilide
  • Anilides
  • Calcium Channel Blockers
  • Calcium Channels
  • Enzyme Inhibitors
  • Imidazoles
  • Indicators and Reagents
  • Indoles
  • Macrocyclic Compounds
  • Oxazoles
  • Ryanodine Receptor Calcium Release Channel
  • Thiadiazoles
  • xestospongin C
  • Thapsigargin
  • Lanthanum
  • Nickel
  • Inositol 1,4,5-Trisphosphate
  • 1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1H-imidazole
  • cyclopiazonic acid

Grants and funding