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      Cell-Type-Specific Control of Brainstem Locomotor Circuits by Basal Ganglia

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          Summary

          The basal ganglia (BG) are critical for adaptive motor control, but the circuit principles underlying their pathway-specific modulation of target regions are not well understood. Here, we dissect the mechanisms underlying BG direct- and indirect-pathway-mediated control of the mesencephalic locomotor region (MLR), a brainstem target of the BG that is critical for locomotion. We optogenetically dissect the locomotor function of the three neurochemically-distinct cell types within the MLR: glutamatergic, GABAergic, and cholinergic neurons. We find that the glutamatergic subpopulation encodes locomotor state and speed, is necessary and sufficient for locomotion, and is selectively innervated by BG. We further show activation and suppression, respectively, of MLR glutamatergic neurons by direct and indirect pathways, which is required for bidirectional control of locomotion by BG circuits. These findings provide a fundamental understanding of how the BG can initiate or suppress a motor program through cell-type-specific regulation of neurons linked to specific actions.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          30 December 2015
          28 January 2016
          28 January 2017
          : 164
          : 3
          : 526-537
          Affiliations
          [1 ]The Gladstone Institutes, San Francisco, CA 94158 USA
          [2 ]Neuroscience Graduate Program, University of California, San Francisco, CA 94158 USA
          [3 ]Medical Scientist Training Program, University of California, San Francisco, CA 94158 USA
          [4 ]Department of Psychology, University of California, Berkeley, CA 94720 USA
          [5 ]Intramural Research Program, Synaptic Plasticity Section, National Institute for Drug Abuse, Baltimore, MD 21224 USA
          [6 ]Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, MD 21205 USA
          [7 ]Department of Psychiatry, Johns Hopkins University, Baltimore, MD 21287 USA
          [8 ]Departments of Physiology and Neurology, University of California, San Francisco, CA 94158 USA
          Author notes
          [* ]correspondence to: akreitzer@ 123456gladstone.ucsf.edu
          [#]

          contributed equally

          Article
          PMC4733247 PMC4733247 4733247 nihpa747874
          10.1016/j.cell.2015.12.037
          4733247
          26824660
          521896f0-df09-438a-9a10-d4293ba5dcd0
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