JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 70: 1669-1680, 1993;
0022-3077/93 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gallemore, R. P.
Right arrow Articles by Steinberg, R. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gallemore, R. P.
Right arrow Articles by Steinberg, R. H.

Journal of Neurophysiology, Vol 70, Issue 4 1669-1680, Copyright © 1993 by APS


ARTICLES

Light-evoked modulation of basolateral membrane Cl- conductance in chick retinal pigment epithelium: the light peak and fast oscillation

R. P. Gallemore and R. H. Steinberg
Department of Physiology, University of California, San Francisco 94143.

1. We studied the ionic mechanism of the light-peak voltage of the DC electroretinogram (DC ERG) in an in vitro preparation of chick neural retina-retinal pigment epithelium (RPE)-choroid. The light peak originates from a depolarization of the RPE basolateral (basal) membrane, associated with an increase in its conductance. Using conventional and Cl(-)-selective microelectrodes, we tested the hypothesis that the light-peak voltage is generated by an increase in Cl- conductance (gCl) of the basolateral (basal) membrane. 2. Perfusion of the RPE basal membrane with 4,4'-diisothiocyanostilbene-2,2'-disulfonate (DIDS), a known blocker of gCl in chick RPE, suppressed both the light-peak depolarization and the accompanying conductance increase of the basal membrane. 3. Using sustained transepithelial current to clamp the basal membrane potential at different levels, we estimated the reversal potential of the light peak. At membrane potentials above the equilibrium potential for Cl- (ECl = -40 +/- 10 mV mean +/- SE), light-peak polarity was reversed. Current-voltage (I-V) curves measured in the dark and at the peak of the light peak also gave a reversal potential in the same range as ECl. In addition, shifting ECl by changing intracellular Cl- (aCli) via passage of transepithelial current or perfusing the apical side of the RPE with the Cl- uptake blocker, furosemide, shifted the light-peak reversal potential in the same direction as the change in ECl. 4. The transference number for Cl-, TCl, was estimated from step decreases in basal Cl- and increased from 0.20 +/- 0.01 in the dark to 0.31 +/- 0.01 during the light peak. These results indicate an average increase of 55% in the relative conductance of the basal membrane for Cl-. 5. Light-evoked changes in aCli, measured with Cl(-)-selective microelectrodes, were too small to account for the change in basal membrane potential during the light peak. These data strongly support the hypothesis that the light peak originates from an increase in RPE basal membrane permeability to Cl-. 6. We also obtained support for the model of Joseph and Miller that the fast-oscillation trough of the DC ERG, generated by a delayed basal membrane hyperpolarization of the RPE, originates from light-evoked modulation of the Cl- transport pathway. Perfusing either the apical side of the RPE with furosemide or the basal side with DIDS suppressed the fast oscillation. The delayed basal hyperpolarization reversed polarity at membrane potentials positive to ECl.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
J. Wu, A. D. Marmorstein, J. Striessnig, and N. S. Peachey
Voltage-Dependent Calcium Channel CaV1.3 Subunits Regulate the Light Peak of the Electroretinogram
J Neurophysiol, May 1, 2007; 97(5): 3731 - 3735.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
K. Yu, Y. Cui, and H. C. Hartzell
The Bestrophin Mutation A243V, Linked to Adult-Onset Vitelliform Macular Dystrophy, Impairs Its Chloride Channel Function
Invest. Ophthalmol. Vis. Sci., November 1, 2006; 47(11): 4956 - 4961.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
D. Reigada, W. Lu, and C. H. Mitchell
Glutamate acts at NMDA receptors on fresh bovine and on cultured human retinal pigment epithelial cells to trigger release of ATP
J. Physiol., September 15, 2006; 575(3): 707 - 720.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
O. Strauss
The Retinal Pigment Epithelium in Visual Function
Physiol Rev, July 1, 2005; 85(3): 845 - 881.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
A. D. Marmorstein, J. B. Stanton, J. Yocom, B. Bakall, M. T. Schiavone, C. Wadelius, L. Y. Marmorstein, and N. S. Peachey
A Model of Best Vitelliform Macular Dystrophy in Rats
Invest. Ophthalmol. Vis. Sci., October 1, 2004; 45(10): 3733 - 3739.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
C. Rahner, M. Fukuhara, S. Peng, S. Kojima, and L. J. Rizzolo
The apical and basal environments of the retinal pigment epithelium regulate the maturation of tight junctions during development
J. Cell Sci., July 1, 2004; 117(15): 3307 - 3318.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Physiol.Home page
Z. Qu, R. Fischmeister, and C. Hartzell
Mouse Bestrophin-2 Is a Bona fide Cl- Channel: Identification of a Residue Important in Anion Binding and Conduction
J. Gen. Physiol., March 29, 2004; 123(4): 327 - 340.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
B. Bakall, L. Y. Marmorstein, G. Hoppe, N. S. Peachey, C. Wadelius, and A. D. Marmorstein
Expression and Localization of Bestrophin during Normal Mouse Development
Invest. Ophthalmol. Vis. Sci., August 1, 2003; 44(8): 3622 - 3628.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
S. A. Rajasekaran, J. Hu, J. Gopal, R. Gallemore, S. Ryazantsev, D. Bok, and A. K. Rajasekaran
Na,K-ATPase inhibition alters tight junction structure and permeability in human retinal pigment epithelial cells
Am J Physiol Cell Physiol, June 1, 2003; 284(6): C1497 - C1507.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
S. Peng, C. Rahner, and L. J. Rizzolo
Apical and Basal Regulation of the Permeability of the Retinal Pigment Epithelium
Invest. Ophthalmol. Vis. Sci., February 1, 2003; 44(2): 808 - 817.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. Y. Marmorstein, P. J. McLaughlin, J. B. Stanton, L. Yan, J. W. Crabb, and A. D. Marmorstein
Bestrophin Interacts Physically and Functionally with Protein Phosphatase 2A
J. Biol. Chem., August 16, 2002; 277(34): 30591 - 30597.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
C.-F. Arndt, A. Sari, M. Ferre, E. Parrat, D. Courtas, J. De Seze, J.-C. Hache, and R. Matran
Electrophysiological Effects of Corticosteroids on the Retinal Pigment Epithelium
Invest. Ophthalmol. Vis. Sci., February 1, 2001; 42(2): 472 - 475.
[Abstract] [Full Text]


Home page
IOVSHome page
R. H. Quinn, J. N. Quong, and S. S. Miller
Adrenergic Receptor Activated Ion Transport in Human Fetal Retinal Pigment Epithelium
Invest. Ophthalmol. Vis. Sci., January 1, 2001; 42(1): 255 - 264.
[Abstract] [Full Text]


Home page
J. Neurosci.Home page
W. M. Peterson, C. Meggyesy, K. Yu, and S. S. Miller
Extracellular ATP Activates Calcium Signaling, Ion, and Fluid Transport in Retinal Pigment Epithelium
J. Neurosci., April 1, 1997; 17(7): 2324 - 2337.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online