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Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation

Light adaptation in vertebrate photoreceptors is thought to be mediated through a number of biochemical feedback reactions that reduce the sensitivity of the photoreceptor and accelerate the kinetics of the photoresponse. Ca(2+) plays a major role in this process by regulating several components of...

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Autores principales: Calvert, Peter D., Ho, Theresa W., LeFebvre, Yvette M., Arshavsky, Vadim Y.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1887766/
https://www.ncbi.nlm.nih.gov/pubmed/9417133
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author Calvert, Peter D.
Ho, Theresa W.
LeFebvre, Yvette M.
Arshavsky, Vadim Y.
author_facet Calvert, Peter D.
Ho, Theresa W.
LeFebvre, Yvette M.
Arshavsky, Vadim Y.
author_sort Calvert, Peter D.
collection PubMed
description Light adaptation in vertebrate photoreceptors is thought to be mediated through a number of biochemical feedback reactions that reduce the sensitivity of the photoreceptor and accelerate the kinetics of the photoresponse. Ca(2+) plays a major role in this process by regulating several components of the phototransduction cascade. Guanylate cyclase and rhodopsin kinase are suggested to be the major sites regulated by Ca(2+). Recently, it was proposed that cGMP may be another messenger of light adaptation since it is able to regulate the rate of transducin GTPase and thus the lifetime of activated cGMP phosphodiesterase. Here we report measurements of the rates at which the changes in Ca(2+) and cGMP are followed by the changes in the rates of corresponding enzymatic reactions in frog rod outer segments. Our data indicate that there is a temporal hierarchy among reactions that underlie light adaptation. Guanylate cyclase activity and rhodopsin phosphorylation respond to changes in Ca(2+) very rapidly, on a subsecond time scale. This enables them to accelerate the falling phase of the flash response and to modulate flash sensitivity during continuous illumination. To the contrary, the acceleration of transducin GTPase, even after significant reduction in cGMP, occurs over several tens of seconds. It is substantially delayed by the slow dissociation of cGMP from the noncatalytic sites for cGMP binding located on cGMP phosphodiesterase. Therefore, cGMP-dependent regulation of transducin GTPase is likely to occur only during prolonged bright illumination.
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spelling pubmed-18877662008-04-22 Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation Calvert, Peter D. Ho, Theresa W. LeFebvre, Yvette M. Arshavsky, Vadim Y. J Gen Physiol Article Light adaptation in vertebrate photoreceptors is thought to be mediated through a number of biochemical feedback reactions that reduce the sensitivity of the photoreceptor and accelerate the kinetics of the photoresponse. Ca(2+) plays a major role in this process by regulating several components of the phototransduction cascade. Guanylate cyclase and rhodopsin kinase are suggested to be the major sites regulated by Ca(2+). Recently, it was proposed that cGMP may be another messenger of light adaptation since it is able to regulate the rate of transducin GTPase and thus the lifetime of activated cGMP phosphodiesterase. Here we report measurements of the rates at which the changes in Ca(2+) and cGMP are followed by the changes in the rates of corresponding enzymatic reactions in frog rod outer segments. Our data indicate that there is a temporal hierarchy among reactions that underlie light adaptation. Guanylate cyclase activity and rhodopsin phosphorylation respond to changes in Ca(2+) very rapidly, on a subsecond time scale. This enables them to accelerate the falling phase of the flash response and to modulate flash sensitivity during continuous illumination. To the contrary, the acceleration of transducin GTPase, even after significant reduction in cGMP, occurs over several tens of seconds. It is substantially delayed by the slow dissociation of cGMP from the noncatalytic sites for cGMP binding located on cGMP phosphodiesterase. Therefore, cGMP-dependent regulation of transducin GTPase is likely to occur only during prolonged bright illumination. The Rockefeller University Press 1998-01-01 /pmc/articles/PMC1887766/ /pubmed/9417133 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Calvert, Peter D.
Ho, Theresa W.
LeFebvre, Yvette M.
Arshavsky, Vadim Y.
Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation
title Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation
title_full Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation
title_fullStr Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation
title_full_unstemmed Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation
title_short Onset of Feedback Reactions Underlying Vertebrate Rod Photoreceptor Light Adaptation
title_sort onset of feedback reactions underlying vertebrate rod photoreceptor light adaptation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1887766/
https://www.ncbi.nlm.nih.gov/pubmed/9417133
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