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      Mapping synaptic input fields of neurons with super-resolution imaging

      research-article
      1 , 1 , 2 , 1 , 2 , 3
      Cell

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          Summary

          As a basic functional unit in neural circuits, each neuron integrates input signals from hundreds to thousands of synapses. Knowledge of the synaptic input fields of individual neurons, including the identity, strength and location of each synapse, is essential for understanding how neurons compute. Here we developed a volumetric super-resolution reconstruction platform for large-volume imaging and automated segmentation of neurons and synapses with molecular identity information. We used this platform to map inhibitory synaptic input fields of On-Off direction-selective ganglion cells (On-Off DSGCs), which are important for computing visual motion direction in the mouse retina. The reconstructions of On-Off DSGCs showed a GABAergic, receptor subtype-specific input field for generating direction selective responses without significant glycinergic inputs for mediating monosynaptic crossover inhibition. These results demonstrate unique capabilities of this super-resolution platform for interrogating neural circuitry.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          25 January 2016
          01 October 2015
          8 October 2015
          08 October 2016
          : 163
          : 2
          : 493-505
          Affiliations
          [1 ]Howard Hughes Medical Institute, Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA
          [2 ]Center for Brain Science, Harvard University, Cambridge, MA 02138, USA
          [3 ]Department of Physics, Harvard University, Cambridge, MA 02138, USA
          Author notes
          [* ]To whom correspondence should be addressed. E-mail: zhuang@ 123456chemistry.harvard.edu
          [4]

          These authors contributed equally to this work.

          Article
          PMC4733473 PMC4733473 4733473 nihpa727594
          10.1016/j.cell.2015.08.033
          4733473
          26435106
          2b3f4ea0-945d-4466-8797-5e99dd52f673
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