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. 1996 Jan 15;490(Pt 2):319–324. doi: 10.1113/jphysiol.1996.sp021146

Control of action potential propagation by intracellular Ca2+ in cultured rat dorsal root ganglion cells.

C Lüscher 1, P Lipp 1, H R Lüscher 1, E Niggli 1
PMCID: PMC1158671  PMID: 8821131

Abstract

1. To assess the role of intracellular Ca2+ in action potential (AP) propagation, whole-cell recordings of cultured dorsal root ganglion (DRG) cells were carried out while Ca2+ was simultaneously measured with a laser-scanning confocal microscope. 2. Flash photolytic liberation of a Ca2+ buffer during trains of APs which partly failed to invade the DRG cell body immediately lowered intracellular Ca2+ and restored safe AP propagation. Furthermore, the speed of the propagated AP was reduced considerably when intracellular Ca2+ was increased by flash photolysis of caged Ca2+. 3. Both results suggest that intracellular Ca2+ regulates the safety factor for AP propagation and may thus provide a control mechanism for synaptic integration, which acts pre- as well as postsynaptically.

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Selected References

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  1. Currie K. P., Wootton J. F., Scott R. H. Activation of Ca(2+)-dependent Cl- currents in cultured rat sensory neurones by flash photolysis of DM-nitrophen. J Physiol. 1995 Jan 15;482(Pt 2):291–307. doi: 10.1113/jphysiol.1995.sp020518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Eckert R., Chad J. E. Inactivation of Ca channels. Prog Biophys Mol Biol. 1984;44(3):215–267. doi: 10.1016/0079-6107(84)90009-9. [DOI] [PubMed] [Google Scholar]
  3. FRANKENHAEUSER B., HODGKIN A. L. The after-effects of impulses in the giant nerve fibres of Loligo. J Physiol. 1956 Feb 28;131(2):341–376. doi: 10.1113/jphysiol.1956.sp005467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Gurney A. M., Tsien R. Y., Lester H. A. Activation of a potassium current by rapid photochemically generated step increases of intracellular calcium in rat sympathetic neurons. Proc Natl Acad Sci U S A. 1987 May;84(10):3496–3500. doi: 10.1073/pnas.84.10.3496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hernández-Cruz A., Sala F., Adams P. R. Subcellular calcium transients visualized by confocal microscopy in a voltage-clamped vertebrate neuron. Science. 1990 Feb 16;247(4944):858–862. doi: 10.1126/science.2154851. [DOI] [PubMed] [Google Scholar]
  6. Heyer E. J., Macdonald R. L. Calcium- and sodium-dependent action potentials of mouse spinal cord and dorsal root ganglion neurons in cell culture. J Neurophysiol. 1982 Apr;47(4):641–655. doi: 10.1152/jn.1982.47.4.641. [DOI] [PubMed] [Google Scholar]
  7. Kostyuk P. G., Veselovsky N. S., Tsyndrenko A. Y. Ionic currents in the somatic membrane of rat dorsal root ganglion neurons-I. Sodium currents. Neuroscience. 1981;6(12):2423–2430. doi: 10.1016/0306-4522(81)90088-9. [DOI] [PubMed] [Google Scholar]
  8. Lipp P., Niggli E. Ratiometric confocal Ca(2+)-measurements with visible wavelength indicators in isolated cardiac myocytes. Cell Calcium. 1993 May;14(5):359–372. doi: 10.1016/0143-4160(93)90040-d. [DOI] [PubMed] [Google Scholar]
  9. Lüscher C., Streit J., Lipp P., Lüscher H. R. Action potential propagation through embryonic dorsal root ganglion cells in culture. II. Decrease of conduction reliability during repetitive stimulation. J Neurophysiol. 1994 Aug;72(2):634–643. doi: 10.1152/jn.1994.72.2.634. [DOI] [PubMed] [Google Scholar]
  10. Lüscher C., Streit J., Quadroni R., Lüscher H. R. Action potential propagation through embryonic dorsal root ganglion cells in culture. I. Influence of the cell morphology on propagation properties. J Neurophysiol. 1994 Aug;72(2):622–633. doi: 10.1152/jn.1994.72.2.622. [DOI] [PubMed] [Google Scholar]
  11. Morad M., Davies N. W., Kaplan J. H., Lux H. D. Inactivation and block of calcium channels by photo-released Ca2+ in dorsal root ganglion neurons. Science. 1988 Aug 12;241(4867):842–844. doi: 10.1126/science.2457253. [DOI] [PubMed] [Google Scholar]
  12. Spira M. E., Yarom Y., Parnas I. Modulation of spike frequency by regions of special axonal geometry and by synaptic inputs. J Neurophysiol. 1976 Jul;39(4):882–899. doi: 10.1152/jn.1976.39.4.882. [DOI] [PubMed] [Google Scholar]
  13. Spruston N., Schiller Y., Stuart G., Sakmann B. Activity-dependent action potential invasion and calcium influx into hippocampal CA1 dendrites. Science. 1995 Apr 14;268(5208):297–300. doi: 10.1126/science.7716524. [DOI] [PubMed] [Google Scholar]
  14. Stoney S. D., Jr Limitations on impulse conduction at the branch point of afferent axons in frog dorsal root ganglion. Exp Brain Res. 1990;80(3):512–524. doi: 10.1007/BF00227992. [DOI] [PubMed] [Google Scholar]
  15. Streit J., Lüscher C., Lüscher H. R. Depression of postsynaptic potentials by high-frequency stimulation in embryonic motoneurons grown in spinal cord slice cultures. J Neurophysiol. 1992 Nov;68(5):1793–1803. doi: 10.1152/jn.1992.68.5.1793. [DOI] [PubMed] [Google Scholar]
  16. Stuart G. J., Sakmann B. Active propagation of somatic action potentials into neocortical pyramidal cell dendrites. Nature. 1994 Jan 6;367(6458):69–72. doi: 10.1038/367069a0. [DOI] [PubMed] [Google Scholar]
  17. Wall P. D. Do nerve impulses penetrate terminal arborizations? A pre-presynaptic control mechanism. Trends Neurosci. 1995 Feb;18(2):99–103. doi: 10.1016/0166-2236(95)93883-y. [DOI] [PubMed] [Google Scholar]

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