The experiments in this proposal are designed to address important outstanding questions in photoreceptor physiology, and to use the most powerful methods presently available to answer these questions. In collaboration with molecular biologists, this project will use animals with targeted mutations in essential photoreceptor proteins in order to probe basic features of photoreceptor function, in direct response to the program objective of the Retinal Disease Program of the NEI to """"""""analyze the mechanisms underlying light adaptation and recovery following phototransduction"""""""". These experiments will take advantage of techniques recently developed in the PI's laboratory that permit the fast perfusion of the small outer segments of mouse rods, and the bleaching and regeneration of pigment in isolated cells. One of the principal goals of this proposal is to ask how rod responses recover after stimulation with light, and what causes this recovery to be accelerated as the intensity of background illumination is increased, so that we become better able to detect change and motion in bright light. Is the rate of photoreceptor recovery modulated by Ca2+, and if so, by what process? Similar approaches will be used to study mechanisms of photoreceptor light adaptation. Recent experiments have shown that adaptation cannot be completely explained by the usually proposed mechanisms of regulation of guanylyl cyclase, rhodopsin phosphorylation, and channel opening, but that a newly discovered component probably produced by modulation of phosphodiesterase also makes an important contribution. Is light adaptation in mammals controlled by outer segment Ca2+ concentration? If so, does Ca2+ regulate the rate of phosphodiesterase decay as well as the rate of cGMP synthesis? Does the desensitization produced by bright bleaching light also have a phosphodiesterase component, and is bleaching desensitization produced by a mechanism essentially identical to the one producing desensitization in maintained background light? If these questions can be answered, they will move photoreceptor transduction in a new direction and stimulate additional research into the biochemistry of vision. Taken together, the experiments of this proposal will contribute to a more detailed understanding of the physiology of G-protein cascades throughout the body.

Public Health Relevance

The great majority of diseases of the retina are caused by disorder or degeneration of the photoreceptors, the cells in the eye that convert light into an electrical signal. This proposal seeks to understand basic mechanisms of photoreceptor function, particularly adaptation to maintained illumination and recovery after exposure to light, which are known to be implicated in genetically inherited retinal diseases including night blindness, bradyopsin, and Leber's amaurosis. This study will support an important program objective of the National Eye Institute of the NIH to analyze the mechanisms underlying light adaptation and recovery following phototransduction, and this work will also contribute to a more detailed understanding of the physiology of signal transduction throughout the body.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY001844-37
Application #
8515409
Study Section
Special Emphasis Panel (ZRG1-CB-G (02))
Program Officer
Neuhold, Lisa
Project Start
1984-07-01
Project End
2017-07-31
Budget Start
2013-08-01
Budget End
2014-07-31
Support Year
37
Fiscal Year
2013
Total Cost
$351,732
Indirect Cost
$114,232
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Arts and Sciences
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Ingram, Norianne T; Sampath, Alapakkam P; Fain, Gordon L (2016) Why are rods more sensitive than cones? J Physiol 594:5415-26
Woodruff, Michael L; Rajala, Ammaji; Fain, Gordon L et al. (2015) Effect of knocking down the insulin receptor on mouse rod responses. Sci Rep 5:7858
Morshedian, Ala; Fain, Gordon L (2015) Single-photon sensitivity of lamprey rods with cone-like outer segments. Curr Biol 25:484-7
Chen, Ching-Kang; Woodruff, Michael L; Fain, Gordon L (2015) Rhodopsin kinase and recoverin modulate phosphodiesterase during mouse photoreceptor light adaptation. J Gen Physiol 145:213-24
Reingruber, Jürgen; Holcman, David; Fain, Gordon L (2015) How rods respond to single photons: Key adaptations of a G-protein cascade that enable vision at the physical limit of perception. Bioessays 37:1243-52
Fain, Gordon L (2015) Phototransduction: Making the Chromophore to See Through the Murk. Curr Biol 25:R1126-7
Woodruff, Michael L; Rajala, Ammaji; Fain, Gordon L et al. (2014) Modulation of mouse rod photoreceptor responses by Grb14 protein. J Biol Chem 289:358-64
Reingruber, Jürgen; Pahlberg, Johan; Woodruff, Michael L et al. (2013) Detection of single photons by toad and mouse rods. Proc Natl Acad Sci U S A 110:19378-83
Chen, Ching-Kang; Woodruff, Michael L; Chen, Frank S et al. (2012) Modulation of mouse rod response decay by rhodopsin kinase and recoverin. J Neurosci 32:15998-6006
Tsang, Stephen H; Woodruff, Michael L; Lin, Chyuan-Sheng et al. (2012) Effect of the ILE86TER mutation in the γ subunit of cGMP phosphodiesterase (PDE6) on rod photoreceptor signaling. Cell Signal 24:181-8

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