Spontaneous waves of excitation, which occur in the developing retina during a specific time period immediately before the onset of vision, are believed to provide important cues for the development of precise neuronal connectivity in the visual system. However, the mechanisms underlying the formation and regulation of these retinal waves are unknown. Studies proposed in this competing renewal application will investigate neuronal interactions important for the generation, propagation, and regulation of spontaneous waves in the developing retina, with an emphasis on neurotransmitter-mediated interactions in starburst amacrine and ganglion cells. Through a set of carefully selected specific aims, these studies will test several critical and specific aspects of the general hypothesis that spontaneous waves in the mammalian retina are mediated, to a large extent, by multiple neurotransmitter systems interacting in a highly coordinated and age-dependent manner.
These specific aims aim to: (1) identify the contribution of the developing cholinergic, glutamatergic, glycinergic, and GABAergic systems to the formation of spontaneous neuronal activity at various stages of retinal development; (2) understand the rhythmicity and temporal regulation of spontaneous retinal waves; and (3) identify the interrelationship among wave dynamics, neuronal activity, and transmitter interaction. To achieve the above aims, cellular physiological and pharmacological experiments have been designed to take advantage of a unique whole-mount retinal preparation, which allows the integration of a number of cutting-edge neurophysiological techniques, including simultaneous Ca2+ imaging and patch-clamp recording, dual patch-clamp recording from identified cell pairs, and particle-delivered fluorescent labeling of living retinal neurons. This comprehensive approach will enable the investigators to obtain, at the synaptic, cellular, and network levels, critical data on retinal waves previously unattainable in other experimental settings. Results from these studies are expected to provide much needed information about neuronal interaction and spontaneous excitation in the developing retina, thus allowing better understanding of visual development and retinal processing in healthy and diseased states.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY010894-08
Application #
6621622
Study Section
Visual Sciences C Study Section (VISC)
Program Officer
Hunter, Chyren
Project Start
1995-08-01
Project End
2006-11-30
Budget Start
2002-12-01
Budget End
2003-11-30
Support Year
8
Fiscal Year
2003
Total Cost
$292,000
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Physiology
Type
Schools of Medicine
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
Kuenzel, Wayne J; Kang, Seong W; Zhou, Z Jimmy (2015) Exploring avian deep-brain photoreceptors and their role in activating the neuroendocrine regulation of gonadal development. Poult Sci 94:786-98
Chen, Minggang; Lee, Seunghoon; Park, Silvia J H et al. (2014) Receptive field properties of bipolar cell axon terminals in direction-selective sublaminas of the mouse retina. J Neurophysiol 112:1950-62
Xu, Hong-ping; Furman, Moran; Mineur, Yann S et al. (2011) An instructive role for patterned spontaneous retinal activity in mouse visual map development. Neuron 70:1115-27
Lee, Seunghoon; Kim, Kyongmin; Zhou, Z Jimmy (2010) Role of ACh-GABA cotransmission in detecting image motion and motion direction. Neuron 68:1159-72
Zhou, Z Jimmy; Lee, Seunghoon (2008) Synaptic physiology of direction selectivity in the retina. J Physiol 586:4371-6
Zheng, Jijian; Lee, Seunghoon; Zhou, Z Jimmy (2006) A transient network of intrinsically bursting starburst cells underlies the generation of retinal waves. Nat Neurosci 9:363-71
Lee, Seunghoon; Zhou, Z Jimmy (2006) The synaptic mechanism of direction selectivity in distal processes of starburst amacrine cells. Neuron 51:787-99
Zheng, Ji-Jian; Lee, Seunghoon; Zhou, Z Jimmy (2004) A developmental switch in the excitability and function of the starburst network in the mammalian retina. Neuron 44:851-64
Casini, G; Dal Monte, M; Fornai, F et al. (2004) Neurokinin 1 receptor expression and substance P physiological actions are developmentally regulated in the rabbit retina. Neuroscience 124:147-60
Syed, Mohsin Md; Lee, Seunghoon; Zheng, Jijian et al. (2004) Stage-dependent dynamics and modulation of spontaneous waves in the developing rabbit retina. J Physiol 560:533-49

Showing the most recent 10 out of 13 publications