Journal
JOURNAL OF NEUROSCIENCE
Volume 36, Issue 26, Pages 6892-6905Publisher
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0572-16.2016
Keywords
amacrine; CNiFER; electrical synapses; nicotinic acetylcholine receptor
Categories
Funding
- National Institutes of Health [R01EY013528, P30EY003176, F31EY024842]
- National Science Foundation Graduate Research Fellowship Program
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Before the maturation of rod and cone photoreceptors, the developing retina relies on light detection by intrinsically photosensitive retinal ganglion cells (ipRGCs) to drive early light-dependent behaviors. ipRGCs are output neurons of the retina; however, they also form functional microcircuits within the retina itself. Whether ipRGC microcircuits exist during development and whether they influence early light detection remain unknown. Here, we investigate the neural circuit that underlies the ipRGC-driven light response in developing mice. We use a combination of calcium imaging, tracer coupling, and electrophysiology experiments to show that ipRGCs form extensive gap junction networks that strongly contribute to the overall light response of the developing retina. Interestingly, we found that gap junction coupling was modulated by spontaneous retinal waves, such that acute blockade of waves dramatically increased the extent of coupling and hence increased the number of light-responsive neurons. Moreover, using an optical sensor, we found that this wave-dependent modulation of coupling is driven by dopamine that is phasically released by retinal waves. Our results demonstrate that ipRGCs form gap junction microcircuits during development that are modulated by retinal waves; these circuits determine the extent of the light response and thus potentially impact the processing of early visual information and light-dependent developmental functions.
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