Cell-type-specific auditory responses in the striatum are shaped by feedforward inhibition

The posterior "tail" region of the striatum receives dense innervation from sensory brain regions and is important for behaviors that require sensorimotor integration. The output neurons of the striatum, D1 and D2 striatal projection neurons (SPNs), which make up the direct and indirect pathways, are thought to play distinct functional roles, although it remains unclear if these neurons show cell-type-specific differences in their response to sensory stimuli. Here, we examine the strength of synaptic inputs onto D1 and D2 SPNs following the stimulation of upstream auditory pathways. We report that auditory-evoked depolarizations onto D1 SPN responses are stronger and faster. This is due to differences in feedforward inhibition, with fast-spiking interneurons forming stronger synapses onto D2 SPNs. Our results support a model in which differences in feedforward inhibition enable the preferential recruitment of D1 SPNs by auditory stimuli, positioning the direct pathway to initiate sound-driven actions.

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Publication Details

Journal
Cell Reports
Published
2024-12-24
DOI
https://doi.org/10.1016/j.celrep.2024.115090
Citations
5
Primary Topic
Neural dynamics and brain function
Type
article
Field-Weighted Citation Impact
1.71

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article

Cell-type-specific auditory responses in the striatum are shaped by feedforward inhibition

Tanya Sippy, Mélanie Druart, Corryn Chaimowitz, Catherine Fan et al.
5 citations
Cell Reports
Neural dynamics and brain function
1.71
article

Cell-type-specific auditory responses in the striatum are shaped by feedforward inhibition

Tanya Sippy, Mélanie Druart, Corryn Chaimowitz, Catherine Fan, Megha Kori
article en
5 citations

Abstract

The posterior "tail" region of the striatum receives dense innervation from sensory brain regions and is important for behaviors that require sensorimotor integration. The output neurons of the striatum, D1 and D2 striatal projection neurons (SPNs), which make up the direct and indirect pathways, are thought to play distinct functional roles, although it remains unclear if these neurons show cell-type-specific differences in their response to sensory stimuli. Here, we examine the strength of synaptic inputs onto D1 and D2 SPNs following the stimulation of upstream auditory pathways. We report that auditory-evoked depolarizations onto D1 SPN responses are stronger and faster. This is due to differences in feedforward inhibition, with fast-spiking interneurons forming stronger synapses onto D2 SPNs. Our results support a model in which differences in feedforward inhibition enable the preferential recruitment of D1 SPNs by auditory stimuli, positioning the direct pathway to initiate sound-driven actions.

Cell ReportsVol. 44(1)
New York University (US)
Brain and Behavior Research Foundation, Whitehall Foundation, McKnight Foundation, Leon Levy Foundation, National Institutes of Health, School of Medicine, New York University
Zero hunger
Openalex Percentile: Top 15%
Neural dynamics and brain function
1.71
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