4.8 Article

Serotonergic Signaling Controls Input-Specific Synaptic Plasticity at Striatal Circuits

Journal

NEURON
Volume 98, Issue 4, Pages 801-+

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2018.04.008

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Funding

  1. Fondation pour la Recherche Medicale [DEQ20150734352]
  2. Simons Foundation [SFARI 400101]
  3. Fondazione Istituto Italiano di Tecnologia
  4. Compagnia di San Paolo [2013 0942]
  5. Fondazione Cariplo [2013 0871]
  6. Brain and Behavior Foundation

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Monoaminergic modulation of cortical and thalamic inputs to the dorsal striatum (DS) is crucial for reward-based learning and action control. While dopamine has been extensively investigated in this context, the synaptic effects of serotonin (5-HT) have been largely unexplored. Here, we investigated how serotonergic signaling affects associative plasticity at glutamatergic synapses on the striatal projection neurons of the direct pathway (dSPNs). Combining chemogenetic and optogenetic approaches reveals that impeding serotonergic signaling preferentially gates spike-timing-dependent long-term depression (t-LTD) at thalamostriatal synapses. This t-LTD requires dampened activity of the 5-HT4 receptor subtype, which we demonstrate controls dendritic Ca2+ signals by regulating BK channel activity, and which preferentially localizes at the dendritic shaft. The synaptic effects of 5-HT signaling at thalamostriatal inputs provide insights into how changes in serotonergic levels associated with behavioral states or pathology affect striatal-dependent processes.

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