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The Journal of Neuroscience, 2000, 20:RC56:1-6
RAPID COMMUNICATION
Differential Effects of Acetylcholine and Glutamate Blockade on
the Spatiotemporal Dynamics of Retinal Waves
Evelyne
Sernagor1,
Stephen J.
Eglen2, and
Michael J.
O'Donovan3
1 Department of Child Health, The Medical School,
University of Newcastle upon Tyne, Newcastle upon Tyne, NE2 4HH, United
Kingdom, 2 Institute for Adaptive and Neural Computation,
Division of Informatics, University of Edinburgh, Edinburgh, EH8 9LW,
United Kingdom, and 3 Laboratory of Neural Control,
National Institute of Neurological Diseases and Stroke, National
Institutes of Health, Bethesda, Maryland 20892
In the immature vertebrate retina, neighboring ganglion cells
express spontaneous bursting activity (SBA), resulting in propagating waves. Previous studies suggest that the spontaneous bursting activity,
asynchronous between the two eyes, controls the refinement of retinal
ganglion cell projections to central visual targets. To understand how
the patterns encoded within the waves contribute to the refinement of
connections in the visual system, it is necessary to understand how
wave propagation is regulated. We have used video-rate calcium imaging
of spontaneous bursting activity in chick embryonic retinal ganglion
cells to show how glutamatergic and cholinergic connections, two major
excitatory synaptic drives involved in spontaneous bursting activity,
contribute differentially to the spatiotemporal patterning of the
waves. During partial blockade of cholinergic connections, cellular
recruitment declines, leading to spatially more restricted waves. The
velocity of wave propagation decreases during partial blockade of
glutamatergic connections, but cellular recruitment remains
substantially higher than during cholinergic blockade, thereby altering
correlations in the activity of neighboring and distant ganglion cells.
These findings show that cholinergic and glutamatergic connections
exert different influences on the spatial and temporal properties of the waves, raising the possibility that they may play distinct roles
during visual development.
Key words:
retinal waves; spatiotemporal properties; chick embryo; glutamate; acetylcholine; visual system development; calcium imaging; retinal ganglion cells
Copyright © 2000 Society for Neuroscience 0270-6474/00/$05.00/0
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