In Intact Mammalian Photoreceptors, Ca2+-dependent Modulation of cGMP-gated Ion Channels Is Detectable in Cones but Not in Rods
Open Access
- 29 December 2003
- journal article
- Published by Rockefeller University Press in The Journal of general physiology
- Vol. 123 (1) , 63-76
- https://doi.org/10.1085/jgp.200308952
Abstract
In the mammalian retina, cone photoreceptors efficiently adapt to changing background light intensity and, therefore, are able to signal small differences in luminance between objects and backgrounds, even when the absolute intensity of the background changes over five to six orders of magnitude. Mammalian rod photoreceptors, in contrast, adapt very little and only at intensities that nearly saturate the amplitude of their photoresponse. In search of a molecular explanation for this observation we assessed Ca2+-dependent modulation of ligand sensitivity in cyclic GMP–gated (CNG) ion channels of intact mammalian rods and cones. Solitary photoreceptors were isolated by gentle proteolysis of ground squirrel retina. Rods and cones were distinguished by whether or not their outer segments bind PNA lectin. We measured membrane currents under voltage-clamp in photoreceptors loaded with Diazo-2, a caged Ca2+ chelator, and fixed concentrations of 8Br-cGMP. At 600 nM free cytoplasmic Ca2+ the midpoint of the cone CNG channels sensitivity to 8BrcGMP, 8BrcGMPK1/2, is ∼2.3 μM. The ligand sensitivity is less in rod than in cone channels. Instantly decreasing cytoplasmic Ca2+ to 2+ -dependent modulation of cone CNG channels, presumably because of an increase in their affinity to the cyclic nucleotide. The time course of current activation is temperature dependent; it is well described by a single exponential process of ∼480 ms time constant at 20–21°C and 138 ms at 32°C. The absence of detectable Ca2+-dependent CNG current modulation in intact rods, in view of the known channel modulation by calmodulin in-vitro, affirms the modulation in intact rods may only occur at low Ca2+ concentrations, those expected at intensities that nearly saturate the rod photoresponse. The correspondence between Ca2+ dependence of CNG modulation and the ability to light adapt suggest these events are correlated in photoreceptors.Keywords
This publication has 64 references indexed in Scilit:
- Functionally Important Calmodulin-binding Sites in Both NH2- and COOH-terminal Regions of the Cone Photoreceptor Cyclic Nucleotide-gated Channel CNGB3 SubunitJournal of Biological Chemistry, 2003
- Ligand sensitivity of the α2 subunit from the bovine cone cGMP‐gated channel is modulated by protein kinase C but not by calmodulinThe Journal of Physiology, 2001
- Modulation of rod, but not cone, cGMP-gated photoreceptor channels by calcium-calmodulinVisual Neuroscience, 1997
- Ca2+ Dependence of Dark- and Light-Adapted Flash Responses in Rod PhotoreceptorsNeuron, 1996
- Modulation of the cGMP-gated channel of rod photoreceptor cells by calmodulinNature, 1993
- Intracellular calibration of the fluorescent calcium indicator Fura-2Cell Calcium, 1990
- Ionic channels of the inner segment of tiger salamander cone photoreceptors.The Journal of general physiology, 1989
- Calcium and calcium-dependent chloride currents generate action potentials in solitary cone photoreceptorsNeuron, 1988
- The photoreceptors of diurnal squirrels: Outer segment structure, disc shedding, and protein renewalJournal of Ultrastructure Research, 1976
- Intracellular recordings from gecko photoreceptors during light and dark adaptation.The Journal of general physiology, 1975