4.8 Article

Segregated Glycine-Glutamate Co-transmission from vGluT3 Amacrine Cells to Contrast-Suppressed and Contrast-Enhanced Retinal Circuits

Journal

NEURON
Volume 90, Issue 1, Pages 27-34

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2016.02.023

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Funding

  1. NIH [EY017353, EY026065]
  2. Research to Prevent Blindness Inc.
  3. China Scholarship Council [201406240139]
  4. Marvin L. Sears Endowed Professorship

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Since the introduction of Dale's principle of one neuron releases one transmitter at all its synapses,'' a growing number of exceptions to this principle have been identified. While the concept of neurotransmitter co-release by a single neuron is now well accepted, the specific synaptic circuitry and functional advantage of co-neurotransmission remain poorly understood in general. Here we report Ca2+-dependent co-release of a new combination of inhibitory and excitatory neurotransmitters, namely, glycine and glutamate, by the vGluT3-expressing amacrine cell (GAC) in the mouse retina. GACs selectively make glycinergic synapses with uniformity detectors (UDs) and provide a major inhibitory drive that underlies the suppressed-by-contrast trigger feature of UDs. Meanwhile, GACs release glutamate to excite OFF alpha ganglion cells and a few other nonlinear, contrast-sensitive ganglion cells. This coordinated inhibition and excitation of two separate neuronal circuits by a single interneuron suggests a unique advantage in differential detection of visual field uniformity and contrast.

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