The experiments described in this proposal are aimed understanding the photoreceptor to On-bipolar cell synapse in the vertebrate retina. The On-bipolar cell uses a G-protein-coupled signaling mechanism to relay information it collects from the photoreceptors to the inner retina for processing. While the receptor and G-protein have been identified, the mechanisms linking these to a non-specific cation channel are unknown. I will approach the study of this cascade with the following strategy. While blocking the G-protein's action, I will determine what internal factors are necessary in On-bipolar cells to open transduction channels. To accomplish this I will make whole-cell patch clamp recordings from salamander On-bipolar cells. In particular I will test whether the native state of the transduction channel is open or closed, and whether gating mechanisms directly or indirectly involve cGMP. If cGMP is not involved, the metabolic requirements for channel opening will be identified. In parallel experiments I will determine what internal factors are necessary for maintaining the light response, or what factors are necessary for channel closure. I will also test inhibitors of other known signaling mechanisms that utilize non-specific cation channels. These two types of experiments will be corroborated by two-photon imaging of calcium in the On-bipolar dendrites, to compare the localization of """"""""run-open"""""""" channels with those opened by the transduction mechanism. Finally, I will study how low light level information is transferred between rod photoreceptors and rod bipolar cells in the mouse retina. The signal-to-noise ratio at this synapse is maximized by a thresholding non-linearity. I will study the mechanism producing this non-linearity. First I will determine whether the mechanism is pre- or postsynaptic, and if it arises from saturation at the receptors or downstream in the transduction mechanism. Lastly, I will determine whether the non-linearity is dynamic, or whether its position can be influenced by very dim background light. ? ?

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32EY014784-02
Application #
6783466
Study Section
Special Emphasis Panel (ZRG1-F02B (20))
Program Officer
Mariani, Andrew P
Project Start
2003-03-16
Project End
2004-12-31
Budget Start
2004-03-16
Budget End
2004-12-31
Support Year
2
Fiscal Year
2004
Total Cost
$41,163
Indirect Cost
Name
University of Washington
Department
Physiology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Matthews, Hugh R; Sampath, Alapakkam P (2010) Photopigment quenching is Ca2+ dependent and controls response duration in salamander L-cone photoreceptors. J Gen Physiol 135:355-66
Dunn, Felice A; Doan, Thuy; Sampath, Alapakkam P et al. (2006) Controlling the gain of rod-mediated signals in the Mammalian retina. J Neurosci 26:3959-70
Sampath, Alapakkam P; Strissel, Katherine J; Elias, Rajesh et al. (2005) Recoverin improves rod-mediated vision by enhancing signal transmission in the mouse retina. Neuron 46:413-20
Sampath, Alapakkam P; Rieke, Fred (2004) Selective transmission of single photon responses by saturation at the rod-to-rod bipolar synapse. Neuron 41:431-43