Neuronal Plasticity in the Retina

Ohio State University, Columbus OH

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Abstract

Project Summary/Abstract This research project is an experimental study that seeks to understand how neuronal networks change or adapt due to the influence of an intrinsic circadian oscillator. Recent published evidence indicates that a circadian (24-hour) clock in the mammalian retina regulates rod and cone input to cone-connected horizontal cells, a type of second order cell that receives synaptic contact from cones, by controlling rod- cone gap junctional coupling via dopamine D2 receptors. Preliminary evidence suggests that the retinal clock also regulates rod and cone input to ganglion cells, the output neurons of the retina. A circadian clock is a type of biological oscillator that has persistent rhythmicity with a period of approximately 24 hours in the absence of external timing cues (e.g. constant darkness). Preliminary evidence suggests that the retinal clock uses the intracellular signaling molecules cyclic AMP and protein kinase A and the neuromodulators melatonin and adenosine, in addition to dopamine, to regulate rod and cone input to cone-connected horizontal cells and to ganglion cells in part via Connexin36-containing gap junctions. We will use electrophysiological, neurochemical and anatomical techniques to determine whether the circadian clock utilizes adenosine and melatonin, and the intracellular signaling molecules cyclic AMP and protein kinase A to control rod and cone input to cones and cone-connected horizontal cells in part by modulating Connexin36- containing rod-cone gap junctions. We will also determine whether the clock utilizes dopamine, adenosine, and melatonin to control rod and cone input to ganglion cells and AII amacrine cells in part by modulating Connexin36-containing gap junctions. The light responses and tracer coupling of neurons in in vitro rabbit, mouse and goldfish retina preparations will be studied in the day and night under conditions of constant darkness.