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. 1993 Mar;462:321–347. doi: 10.1113/jphysiol.1993.sp019558

Photo-released intracellular Ca2+ rapidly blocks Ba2+ current in Lymnaea neurons.

B D Johnson 1, L Byerly 1
PMCID: PMC1175304  PMID: 8331587

Abstract

1. The effect of intracellular Ca2+ on Ba2+ current flowing through voltage-dependent Ca2+ channels was studied using the whole-cell patch-clamp technique on isolated neurons from the snail Lymnaea stagnalis. Intracellular Ca2+ was increased by flash photolysis of the caged Ca2+ compound DM-nitrophen and measured with the optical indicator fluo-3. 2. After the highest intensity flashes, peak Ba2+ current was blocked by 42% with a time constant of 5 ms. The onset of the block followed a similar time course whether channels were activated or closed. The Ba2+ current surviving after the flash had the same voltage dependence of activation and rate of inactivation as did the total Ba2+ current before the flash. 3. Recovery of the Ba2+ current from block was nearly complete and occurred with a time constant of 16 s. Multiple episodes of photolysis-induced block could be studied in the same cell when 7-10 min were allowed between flashes. In some cells, recovery from block was accompanied by a transient enhancement of the current above the pre-block magnitude. 4. Neurons greatly reduced the ability of photolysis to increase Ca2+, both by unloading the DM-nitrophen before flashes were applied and by rapidly buffering the photolytically released Ca2+. Maximal flashes on extracellular droplets of the DM-Ca2+ solution created a Ca2+ jump from 110 nM to 40 microM. In contrast, the same flashes on DM-Ca(2+)-loaded neurons resulted in a Ca2+ transient starting from a baseline of 36 nM to a peak of 130 nM. This intracellular Ca2+ transient decayed with three time constants (120 ms, 2 s and 13 s). 5. Endogenous buffer(s) binds Ca2+ rapidly. When intracellular Ca2+ was monitored within 2 ms of the flash, no rapid Ca2+ spike due to binding of photo-released Ca2+ could be detected. Addition of dibromo-BAPTA to the intracellular solution reduced the block by one third, which is consistent with the measured reduction of intracellular Ca2+. This indicates that the endogenous buffer can bind Ca2+ as rapidly as dibromo-BAPTA and as fast as Ca2+ is released by photolysis. 6. The Ca2+ dependence of the block, obtained by varying flash intensity, indicates some saturation by 130 nM. A simple two-state model of the block consistent with both the time course of block and recovery and the concentration dependence gave a dissociation constant of approximately 50 nM and forward rate constant of 7 x 10(8) M-1 s-1.(ABSTRACT TRUNCATED AT 400 WORDS)

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Akaike N., Tsuda Y., Oyama Y. Separation of current- and voltage-dependent inactivation of calcium current in frog sensory neuron. Neurosci Lett. 1988 Jan 11;84(1):46–50. doi: 10.1016/0304-3940(88)90335-7. [DOI] [PubMed] [Google Scholar]
  2. Augustine G. J., Charlton M. P., Horn R. Role of calcium-activated potassium channels in transmitter release at the squid giant synapse. J Physiol. 1988 Apr;398:149–164. doi: 10.1113/jphysiol.1988.sp017035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Brehm P., Eckert R. Calcium entry leads to inactivation of calcium channel in Paramecium. Science. 1978 Dec 15;202(4373):1203–1206. doi: 10.1126/science.103199. [DOI] [PubMed] [Google Scholar]
  4. Byerly L., Moody W. J. Intracellular calcium ions and calcium currents in perfused neurones of the snail, Lymnaea stagnalis. J Physiol. 1984 Jul;352:637–652. doi: 10.1113/jphysiol.1984.sp015314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Byerly L., Suen Y. Characterization of proton currents in neurones of the snail, Lymnaea stagnalis. J Physiol. 1989 Jun;413:75–89. doi: 10.1113/jphysiol.1989.sp017642. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Byerly L., Yazejian B. Intracellular factors for the maintenance of calcium currents in perfused neurones from the snail, Lymnaea stagnalis. J Physiol. 1986 Jan;370:631–650. doi: 10.1113/jphysiol.1986.sp015955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Campbell D. L., Giles W. R., Hume J. R., Shibata E. F. Inactivation of calcium current in bull-frog atrial myocytes. J Physiol. 1988 Sep;403:287–315. doi: 10.1113/jphysiol.1988.sp017250. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chad J. E., Eckert R. An enzymatic mechanism for calcium current inactivation in dialysed Helix neurones. J Physiol. 1986 Sep;378:31–51. doi: 10.1113/jphysiol.1986.sp016206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Connor J. A., Ahmed Z. Diffusion of ions and indicator dyes in neural cytoplasm. Cell Mol Neurobiol. 1984 Mar;4(1):53–66. doi: 10.1007/BF00710942. [DOI] [PubMed] [Google Scholar]
  10. Eberhard M., Erne P. Kinetics of calcium binding to fluo-3 determined by stopped-flow fluorescence. Biochem Biophys Res Commun. 1989 Aug 30;163(1):309–314. doi: 10.1016/0006-291x(89)92136-0. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. Grell E., Lewitzki E., Ruf H., Bamberg E., Ellis-Davies G. C., Kaplan J. H., de Weer P. Caged-Ca2+: a new agent allowing liberation of free Ca2+ in biological systems by photolysis. Cell Mol Biol. 1989;35(5):515–522. [PubMed] [Google Scholar]
  13. Gurney A. M., Charnet P., Pye J. M., Nargeot J. Augmentation of cardiac calcium current by flash photolysis of intracellular caged-Ca2+ molecules. Nature. 1989 Sep 7;341(6237):65–68. doi: 10.1038/341065a0. [DOI] [PubMed] [Google Scholar]
  14. 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]
  15. Gutnick M. J., Lux H. D., Swandulla D., Zucker H. Voltage-dependent and calcium-dependent inactivation of calcium channel current in identified snail neurones. J Physiol. 1989 May;412:197–220. doi: 10.1113/jphysiol.1989.sp017611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hadley R. W., Hume J. R. An intrinsic potential-dependent inactivation mechanism associated with calcium channels in guinea-pig myocytes. J Physiol. 1987 Aug;389:205–222. doi: 10.1113/jphysiol.1987.sp016654. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hagiwara S., Nakajima S. Effects of the intracellular Ca ion concentration upon the excitability of the muscle fiber membrane of a barnacle. J Gen Physiol. 1966 Mar;49(4):807–818. doi: 10.1085/jgp.49.4.807. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Huang Y., Quayle J. M., Worley J. F., Standen N. B., Nelson M. T. External cadmium and internal calcium block of single calcium channels in smooth muscle cells from rabbit mesenteric artery. Biophys J. 1989 Nov;56(5):1023–1028. doi: 10.1016/S0006-3495(89)82747-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kao J. P., Harootunian A. T., Tsien R. Y. Photochemically generated cytosolic calcium pulses and their detection by fluo-3. J Biol Chem. 1989 May 15;264(14):8179–8184. [PubMed] [Google Scholar]
  20. Kaplan J. H., Ellis-Davies G. C. Photolabile chelators for the rapid photorelease of divalent cations. Proc Natl Acad Sci U S A. 1988 Sep;85(17):6571–6575. doi: 10.1073/pnas.85.17.6571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kostyuk P. G., Krishtal O. A. Effects of calcium and calcium-chelating agents on the inward and outward current in the membrane of mollusc neurones. J Physiol. 1977 Sep;270(3):569–580. doi: 10.1113/jphysiol.1977.sp011969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Lee K. S., Marban E., Tsien R. W. Inactivation of calcium channels in mammalian heart cells: joint dependence on membrane potential and intracellular calcium. J Physiol. 1985 Jul;364:395–411. doi: 10.1113/jphysiol.1985.sp015752. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Marban E., Tsien R. W. Enhancement of calcium current during digitalis inotropy in mammalian heart: positive feed-back regulation by intracellular calcium? J Physiol. 1982 Aug;329:589–614. doi: 10.1113/jphysiol.1982.sp014321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. McCleskey E. W., Fox A. P., Feldman D., Tsien R. W. Different types of calcium channels. J Exp Biol. 1986 Sep;124:177–190. doi: 10.1242/jeb.124.1.177. [DOI] [PubMed] [Google Scholar]
  25. 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]
  26. Ohya Y., Kitamura K., Kuriyama H. Regulation of calcium current by intracellular calcium in smooth muscle cells of rabbit portal vein. Circ Res. 1988 Feb;62(2):375–383. doi: 10.1161/01.res.62.2.375. [DOI] [PubMed] [Google Scholar]
  27. Plant T. D., Standen N. B., Ward T. A. The effects of injection of calcium ions and calcium chelators on calcium channel inactivation in Helix neurones. J Physiol. 1983 Jan;334:189–212. doi: 10.1113/jphysiol.1983.sp014489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Rapp G., Güth K. A low cost high intensity flash device for photolysis experiments. Pflugers Arch. 1988 Feb;411(2):200–203. doi: 10.1007/BF00582315. [DOI] [PubMed] [Google Scholar]
  29. Robertson S. P., Johnson J. D., Potter J. D. The time-course of Ca2+ exchange with calmodulin, troponin, parvalbumin, and myosin in response to transient increases in Ca2+. Biophys J. 1981 Jun;34(3):559–569. doi: 10.1016/S0006-3495(81)84868-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Rosenberg R. L., Hess P., Tsien R. W. Cardiac calcium channels in planar lipid bilayers. L-type channels and calcium-permeable channels open at negative membrane potentials. J Gen Physiol. 1988 Jul;92(1):27–54. doi: 10.1085/jgp.92.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Sala F., Hernández-Cruz A. Calcium diffusion modeling in a spherical neuron. Relevance of buffering properties. Biophys J. 1990 Feb;57(2):313–324. doi: 10.1016/S0006-3495(90)82533-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Sherman A., Keizer J., Rinzel J. Domain model for Ca2(+)-inactivation of Ca2+ channels at low channel density. Biophys J. 1990 Oct;58(4):985–995. doi: 10.1016/S0006-3495(90)82443-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Simon S. M., Llinás R. R. Compartmentalization of the submembrane calcium activity during calcium influx and its significance in transmitter release. Biophys J. 1985 Sep;48(3):485–498. doi: 10.1016/S0006-3495(85)83804-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Smith G. A., Hesketh R. T., Metcalfe J. C., Feeney J., Morris P. G. Intracellular calcium measurements by 19F NMR of fluorine-labeled chelators. Proc Natl Acad Sci U S A. 1983 Dec;80(23):7178–7182. doi: 10.1073/pnas.80.23.7178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Tillotson D. Inactivation of Ca conductance dependent on entry of Ca ions in molluscan neurons. Proc Natl Acad Sci U S A. 1979 Mar;76(3):1497–1500. doi: 10.1073/pnas.76.3.1497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Tsien R. Y., Rink T. J. Neutral carrier ion-selective microelectrodes for measurement of intracellular free calcium. Biochim Biophys Acta. 1980 Jul;599(2):623–638. doi: 10.1016/0005-2736(80)90205-9. [DOI] [PubMed] [Google Scholar]
  37. Yue D. T., Backx P. H., Imredy J. P. Calcium-sensitive inactivation in the gating of single calcium channels. Science. 1990 Dec 21;250(4988):1735–1738. doi: 10.1126/science.2176745. [DOI] [PubMed] [Google Scholar]
  38. Zucker R. S. Effects of photolabile calcium chelators on fluorescent calcium indicators. Cell Calcium. 1992 Jan;13(1):29–40. doi: 10.1016/0143-4160(92)90027-p. [DOI] [PubMed] [Google Scholar]

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