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Nr4a1 suppresses cocaine-induced behavior via epigenetic regulation of homeostatic target genes

Author

Listed:
  • Marco D. Carpenter

    (University of Pennsylvania
    University of Pennsylvania
    University of Pennsylvania)

  • Qiwen Hu

    (University of Pennsylvania
    University of Pennsylvania
    University of Pennsylvania)

  • Allison M. Bond

    (University of Pennsylvania
    University of Pennsylvania)

  • Sonia I. Lombroso

    (University of Pennsylvania
    University of Pennsylvania
    University of Pennsylvania)

  • Kyle S. Czarnecki

    (University of Pennsylvania
    University of Pennsylvania
    University of Pennsylvania)

  • Carissa J. Lim

    (University of Pennsylvania)

  • Hongjun Song

    (University of Pennsylvania
    University of Pennsylvania)

  • Mathieu E. Wimmer

    (Temple University)

  • R. Christopher Pierce

    (Perelman School of Medicine at the University of Pennsylvania)

  • Elizabeth A. Heller

    (University of Pennsylvania
    University of Pennsylvania
    University of Pennsylvania)

Abstract

Endogenous homeostatic mechanisms can restore normal neuronal function following cocaine-induced neuroadaptations. Such mechanisms may be exploited to develop novel therapies for cocaine addiction, but a molecular target has not yet been identified. Here we profiled mouse gene expression during early and late cocaine abstinence to identify putative regulators of neural homeostasis. Cocaine activated the transcription factor, Nr4a1, and its target gene, Cartpt, a key molecule involved in dopamine metabolism. Sustained activation of Cartpt at late abstinence was coupled with depletion of the repressive histone modification, H3K27me3, and enrichment of activating marks, H3K27ac and H3K4me3. Using both CRISPR-mediated and small molecule Nr4a1 activation, we demonstrated the direct causal role of Nr4a1 in sustained activation of Cartpt and in attenuation of cocaine-evoked behavior. Our findings provide evidence that targeting abstinence-induced homeostatic gene expression is a potential therapeutic target in cocaine addiction.

Suggested Citation

  • Marco D. Carpenter & Qiwen Hu & Allison M. Bond & Sonia I. Lombroso & Kyle S. Czarnecki & Carissa J. Lim & Hongjun Song & Mathieu E. Wimmer & R. Christopher Pierce & Elizabeth A. Heller, 2020. "Nr4a1 suppresses cocaine-induced behavior via epigenetic regulation of homeostatic target genes," Nature Communications, Nature, vol. 11(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-14331-y
    DOI: 10.1038/s41467-020-14331-y
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    Cited by:

    1. Marco D. Carpenter & Delaney K. Fischer & Shuo Zhang & Allison M. Bond & Kyle S. Czarnecki & Morgan T. Woolf & Hongjun Song & Elizabeth A. Heller, 2022. "Cell-type specific profiling of histone post-translational modifications in the adult mouse striatum," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Brandon W. Hughes & Jessica L. Huebschman & Evgeny Tsvetkov & Benjamin M. Siemsen & Kirsten K. Snyder & Rose Marie Akiki & Daniel J. Wood & Rachel D. Penrod & Michael D. Scofield & Stefano Berto & Mak, 2024. "NPAS4 supports cocaine-conditioned cues in rodents by controlling the cell type-specific activation balance in the nucleus accumbens," Nature Communications, Nature, vol. 15(1), pages 1-18, December.

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