Cell-Type-Specific Regulation of Nucleus Accumbens Synaptic Plasticity and Cocaine Reward Sensitivity by the Circadian Protein, NPAS2

• Published in: The Journal of neuroscience Vol. 39; no. 24; pp. 4657 - 4667
• Main Authors: Parekh, Puja K, Logan, Ryan W, Ketchesin, Kyle D, Becker-Krail, Darius, Shelton, Micah A, Hildebrand, Mariah A, Barko, Kelly, Huang, Yanhua H, McClung, Colleen A
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 12.06.2019
• Subjects: Adaptation; Animals; Basic Helix-Loop-Helix Transcription Factors - genetics; Behavior; Behavioral plasticity; Circadian rhythms; Cocaine; Cocaine - pharmacology; Cocaine-Related Disorders - genetics; Conditioning; Disruption; Dopamine; Dopamine D1 receptors; Dopamine D2 receptors; Female; Forebrain; Glutamatergic transmission; Glutamic Acid - physiology; Male; Mental disorders; Mice; Mice, Inbred C57BL; Mice, Knockout; Neostriatum; Nerve Tissue Proteins - genetics; Neuronal Plasticity - drug effects; Neuronal Plasticity - genetics; NPAS2 protein; Nuclei (cytology); Nucleus accumbens; Nucleus Accumbens - cytology; Nucleus Accumbens - drug effects; Place preference conditioning; Reinforcement; Reward; RNA viruses; Sensitivity; Spiny neurons; Substrates; Synapses; Synaptic plasticity; Synaptic strength; Synaptic transmission; Synaptic Transmission - drug effects; Viruses; transcription factor; nucleus accumbens; circadian rhythms; cocaine; glutamatergic
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.2233-18.2019

The circadian transcription factor neuronal PAS domain 2 (NPAS2) is linked to psychiatric disorders associated with altered reward sensitivity. The expression of is preferentially enriched in the mammalian forebrain, including the nucleus accumbens (NAc), a major neural substrate of motivated and reward behavior. Previously, we demonstrated that downregulation of NPAS2 in the NAc reduces the conditioned behavioral response to cocaine in mice. We also showed that is preferentially enriched in dopamine receptor 1 containing medium spiny neurons (D1R-MSNs) of the striatum. To extend these studies, we investigated the impact of NPAS2 disruption on accumbal excitatory synaptic transmission and strength, along with the behavioral sensitivity to cocaine reward in a cell-type-specific manner. Viral-mediated knockdown of in the NAc of male and female C57BL/6J mice increased the excitatory drive onto MSNs. Using -tdTomato mice in combination with viral knockdown, we determined these synaptic adaptations were specific to D1R-MSNs relative to non-D1R-MSNs. Interestingly, NAc-specific knockdown of blocked cocaine-induced enhancement of synaptic strength and glutamatergic transmission specifically onto D1R-MSNs. Last, we designed, validated, and used a novel Cre-inducible short-hairpin RNA virus for MSN-subtype-specific knockdown of Cell-type-specific knockdown in D1R-MSNs, but not D2R-MSNs, in the NAc reduced cocaine conditioned place preference. Together, our results demonstrate that NPAS2 regulates excitatory synapses of D1R-MSNs in the NAc and cocaine reward-related behavior. Drug addiction is a widespread public health concern often comorbid with other psychiatric disorders. Disruptions of the circadian clock can predispose or exacerbate substance abuse in vulnerable individuals. We demonstrate a role for the core circadian protein, NPAS2, in mediating glutamatergic neurotransmission at medium spiny neurons (MSNs) in the nucleus accumbens (NAc), a region critical for reward processing. We find that NPAS2 negatively regulates functional excitatory synaptic plasticity in the NAc and is necessary for cocaine-induced plastic changes in MSNs expressing the dopamine 1 receptor (D1R). We further demonstrate disruption of NPAS2 in D1R-MSNs produces augmented cocaine preference. These findings highlight the significance of cell-type-specificity in mechanisms underlying reward regulation by NPAS2 and extend our knowledge of its function.