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Articles, Systems/Circuits

Conditional Knock-Out of Vesicular GABA Transporter Gene from Starburst Amacrine Cells Reveals the Contributions of Multiple Synaptic Mechanisms Underlying Direction Selectivity in the Retina

Zhe Pei, Qiang Chen, David Koren, Benno Giammarinaro, Hector Acaron Ledesma and Wei Wei
Journal of Neuroscience 23 September 2015, 35 (38) 13219-13232; DOI: https://doi.org/10.1523/JNEUROSCI.0933-15.2015
Zhe Pei
Department of Neurobiology, The University of Chicago, Chicago, Illinois 60637
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Qiang Chen
Department of Neurobiology, The University of Chicago, Chicago, Illinois 60637
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David Koren
Department of Neurobiology, The University of Chicago, Chicago, Illinois 60637
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Benno Giammarinaro
Department of Neurobiology, The University of Chicago, Chicago, Illinois 60637
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Hector Acaron Ledesma
Department of Neurobiology, The University of Chicago, Chicago, Illinois 60637
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Wei Wei
Department of Neurobiology, The University of Chicago, Chicago, Illinois 60637
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Abstract

Direction selectivity of direction-selective ganglion cells (DSGCs) in the retina results from patterned excitatory and inhibitory inputs onto DSGCs during motion stimuli. The inhibitory inputs onto DSGCs are directionally tuned to the antipreferred (null) direction and therefore potently suppress spiking during motion in the null direction. However, whether direction-selective inhibition is indispensable for direction selectivity is unclear. Here, we selectively eliminated the directional tuning of inhibitory inputs onto DSGCs by disrupting GABA release from the presynaptic interneuron starburst amacrine cell in the mouse retina. We found that, even without directionally tuned inhibition, direction selectivity can still be implemented in a subset of On-Off DSGCs by direction-selective excitation and a temporal offset between excitation and isotropic inhibition. Our results therefore demonstrate the concerted action of multiple synaptic mechanisms for robust direction selectivity in the retina.

SIGNIFICANCE STATEMENT The direction-selective circuit in the retina has been a classic model to study neural computations by the brain. An important but unresolved question is how direction selectivity is implemented by directionally tuned excitatory and inhibitory mechanisms. Here we specifically removed the direction tuning of inhibition from the circuit. We found that direction tuning of inhibition is important but not indispensable for direction selectivity of DSGCs' spiking activity, and that the residual direction selectivity is implemented by direction-selective excitation and temporal offset between excitation and inhibition. Our results highlight the concerted actions of synaptic excitation and inhibition required for robust direction selectivity in the retina and provide critical insights into how patterned excitation and inhibition collectively implement sensory processing.

  • direction selectivity
  • retina
  • starburst amacrine cell
  • synaptic excitation
  • synaptic inhibition
  • vesicular GABA transporter
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The Journal of Neuroscience: 35 (38)
Journal of Neuroscience
Vol. 35, Issue 38
23 Sep 2015
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Conditional Knock-Out of Vesicular GABA Transporter Gene from Starburst Amacrine Cells Reveals the Contributions of Multiple Synaptic Mechanisms Underlying Direction Selectivity in the Retina
Zhe Pei, Qiang Chen, David Koren, Benno Giammarinaro, Hector Acaron Ledesma, Wei Wei
Journal of Neuroscience 23 September 2015, 35 (38) 13219-13232; DOI: 10.1523/JNEUROSCI.0933-15.2015

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Conditional Knock-Out of Vesicular GABA Transporter Gene from Starburst Amacrine Cells Reveals the Contributions of Multiple Synaptic Mechanisms Underlying Direction Selectivity in the Retina
Zhe Pei, Qiang Chen, David Koren, Benno Giammarinaro, Hector Acaron Ledesma, Wei Wei
Journal of Neuroscience 23 September 2015, 35 (38) 13219-13232; DOI: 10.1523/JNEUROSCI.0933-15.2015
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Keywords

  • direction selectivity
  • retina
  • starburst amacrine cell
  • synaptic excitation
  • synaptic inhibition
  • vesicular GABA transporter

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