Literature DB >> 17734

Surface potential reflected in both gating and permeation mechanisms of sodium and calcium channels of the tunicate egg cell membrane.

H Ohmori, M Yoshii.   

Abstract

1. Threshold changes of Na and Ca currents due to various polyvalent cations (stabilizing cations) or H(+) ions were studied in the egg cell membrane of a tunicate, Halocynthia roretzi, by using the voltage-clamp technique.2. With an increase in [Ca](o) or a decrease in pH in the external solution, the current-voltage (I-V) relations for the peak of the Na and Ca currents shifted along the voltage axis in the positive direction. These voltage shifts in the I-V relations, measured at a potential of V((1/2)) where inward current attains its half-maximum, were shown to be identical to shifts in voltage-dependence of the time courses of Na and Ca currents, and also identical to shifts in the inactivation curves of Na current along the voltage axis.3. The shifts in V((1/2)) produced by various polyvalent cations or H(+) ions were analysed by the Gouy-Chapman equation for the diffuse double layer, by assuming that a change in V((1/2)) directly corresponds to a change in the surface double layer potential.4. The V((1/2))-divalent cation concentration relations of Na current were exactly described by the predictions of the theory with a constant value of the surface charge density of 1e(-)/(9 A)(2). The weak stabilizing effects of Mg(2+), Sr(2+) and Ba(2+) were quite similar to each other and were explained in terms of a ;screening' effect. Other divalent cations, such as Ca(2+), Mn(2+) and Ni(2+), showed various different stabilizing effects which were explained in terms of a ;binding' effect. The binding constants (K(1)'s) for Ca(2+), Mn(2+) and Ni(2+) were 0.21, 0.45 and 0.94 M(-1), respectively.5. H(+) ions showed a powerful stabilizing effect upon the Na current with a K(H) of 6 x 10(4)M(-1). This value indicates that the acidic sites around Na channels have a pK(a) of 4.78. La(3+) ions also acted as a strong stabilizer upon the Na current with a K(La) of 15 M(-1). For both H(+) and La(3+), the V((1/2))-concentration relations were also exactly described by the Gouy-Chapman equation with the same charge density of 1e(-)/(9 A)(2) as estimated by varying divalent cations.6. The stabilizing effect of permeant cations such as Ca(2+), Sr(2+) and Ba(2+) on Ca channel currents was analysed. The effect of lowering pH was also studied. It was found that the surface charge density of 1e(-)/(9 A)(2) estimated by Na current is also applicable to the explanation for the V((1/2))-divalent cation concentration or - pH relationships. The estimated binding constants for H(+), Ca(2+) and Sr(2+) were 1.2x10(5), 0.58 and 0.035 M(-1), respectively. Ba(2+) does not bind to charged sites near to the Ca channels.7. It was noticed that a considerable reduction in the conductances of Na and Ca currents occurred in parallel with a stabilizing effect. This reduction was ascribed to a decrease in the concentration of permeant cations at the external surface of the cell membrane, as predicted by the theory of the diffuse double layer. The Goldman, Hodgkin-Katz equation for ionic currents was applied to explain the conductance suppression.8. The conductance suppressions of Na and Ca channel currents due to Ca(2+), Sr(2+) and Ba(2+) were found to be apparent ones, only reflecting decreases in the surface concentration of permeant cations without any changes in the permeability. After correction for the apparent suppression, the real permeability ratio among Ca(2+), Sr(2+) and Ba(2+) for Ca channels was determined as 1.00, 0.56 and 0.21 respectively.9. The conductance suppression of Na current by lowering pH was explained in terms of a real suppression or blocking which is superimposed on the apparent suppression. Considering the surface [Na](o), the plot of P(Na) against the surface pH yielded a blocking curve of Na channel by H(+) ions, which implies that two H(+) ions are necessary to block each Na channel. For Ca channels no real blockage was observed in acidic pH.10. It was concluded from the present experiment that there exists a surface potential capable of affecting both gating and permeation mechanisms of ionic channels in this tunicate egg cell membrane.

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Year:  1977        PMID: 17734      PMCID: PMC1283623          DOI: 10.1113/jphysiol.1977.sp011821

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  42 in total

1.  The interactions of calcium with mpyxicola giant axons and a description in terms of a simple surface charge model.

Authors:  C L Schauf
Journal:  J Physiol       Date:  1975-07       Impact factor: 5.182

2.  Membrane currents of the tunicate egg under the voltage-clamp condition.

Authors:  H Okamoto; K Takahashi; M Yoshii
Journal:  J Physiol       Date:  1976-01       Impact factor: 5.182

3.  Two components of the calcium current in the egg cell membrane of the tunicate.

Authors:  H Okamoto; K Takahashi; M Yoshii
Journal:  J Physiol       Date:  1976-02       Impact factor: 5.182

4.  Axonal surface charges: binding or screening by divalent cations governed by external pH.

Authors:  J S D'Arrigo
Journal:  J Physiol       Date:  1974-12       Impact factor: 5.182

5.  Ionic pores, gates, and gating currents.

Authors:  C M Armstrong
Journal:  Q Rev Biophys       Date:  1974-05       Impact factor: 5.318

6.  Ruthenium red and violet. I. Chemistry, purification, methods of use for electron microscopy and mechanism of action.

Authors:  J H Luft
Journal:  Anat Rec       Date:  1971-11

7.  An essential ionized acid group in sodium channels.

Authors:  B Hille
Journal:  Fed Proc       Date:  1975-04

8.  Ionic conductance changes in voltage clamped crayfish axons at low pH.

Authors:  P Shrager
Journal:  J Gen Physiol       Date:  1974-12       Impact factor: 4.086

9.  Magnitude and location of surface charges on Myxicola giant axons.

Authors:  T Begenisich
Journal:  J Gen Physiol       Date:  1975-07       Impact factor: 4.086

10.  Ionic blockage of sodium channels in nerve.

Authors:  A M Woodhull
Journal:  J Gen Physiol       Date:  1973-06       Impact factor: 4.086

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  85 in total

1.  The influence of plasma membrane electrostatic properties on the stability of cell ionic composition.

Authors:  S Genet; R Costalat; J Burger
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

2.  Intra and extracellular surface charges near Ca2+ channels in neurons and neuroblastoma cells.

Authors:  A Becchetti; A Arcangeli; M R Del Bene; M Olivotto; E Wanke
Journal:  Biophys J       Date:  1992-10       Impact factor: 4.033

3.  Inactivating and non-inactivating dihydropyridine-sensitive Ca2+ channels in mouse cerebellar granule cells.

Authors:  P A Slesinger; J B Lansman
Journal:  J Physiol       Date:  1991-08       Impact factor: 5.182

4.  Effects of the external pH on Ca channels: experimental studies and theoretical considerations using a two-site, two-ion model.

Authors:  T Iijima; S Ciani; S Hagiwara
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

5.  Dihydropyridine-sensitive low-threshold calcium channels in isolated rat hypothalamic neurones.

Authors:  N Akaike; P G Kostyuk; Y V Osipchuk
Journal:  J Physiol       Date:  1989-05       Impact factor: 5.182

6.  GABA receptor-channel complex as a target site of mercury, copper, zinc, and lanthanides.

Authors:  T Narahashi; J Y Ma; O Arakawa; E Reuveny; M Nakahiro
Journal:  Cell Mol Neurobiol       Date:  1994-12       Impact factor: 5.046

7.  Brain-derived neurotrophic factor enhances the excitability of rat sensory neurons through activation of the p75 neurotrophin receptor and the sphingomyelin pathway.

Authors:  Y H Zhang; Xian Xuan Chi; G D Nicol
Journal:  J Physiol       Date:  2008-05-01       Impact factor: 5.182

8.  Permeation and gating in CaV3.1 (alpha1G) T-type calcium channels effects of Ca2+, Ba2+, Mg2+, and Na+.

Authors:  Nilofar Khan; I Patrick Gray; Carlos A Obejero-Paz; Stephen W Jones
Journal:  J Gen Physiol       Date:  2008-08       Impact factor: 4.086

9.  Regulation of N-type voltage-gated calcium channels (Cav2.2) and transmitter release by collapsin response mediator protein-2 (CRMP-2) in sensory neurons.

Authors:  Xian Xuan Chi; Brian S Schmutzler; Joel M Brittain; Yuying Wang; Cynthia M Hingtgen; Grant D Nicol; Rajesh Khanna
Journal:  J Cell Sci       Date:  2009-11-10       Impact factor: 5.285

10.  The whole-cell calcium current in acutely dissociated magnocellular cholinergic basal forebrain neurones of the rat.

Authors:  T G Allen; J A Sim; D A Brown
Journal:  J Physiol       Date:  1993-01       Impact factor: 5.182

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