Behavioral and structural responses to chronic cocaine require a feedforward loop involving Δ FosB and calcium/ calmodulin-dependent protein kinase II in the nucleus accumbens shell

Alfred J. Robison, Vincent Vialou, Michelle Mazei-Robison, Jian Feng, Saïd Kourrich, Miles Collins, Sunmee Wee, George Koob, Gustavo Turecki, Rachael Neve, Mark Thomas, Eric J. Nestler

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102 Scopus citations

Abstract

The transcription factor Δ FosB and the brain-enriched calcium/calmodulin-dependent protein kinase II (CaMKIIα) are induced in the nucleus accumbens (NAc) by chronic exposure to cocaine or other psychostimulant drugs of abuse, in which the two proteins mediate sensitized drug responses. Although Δ FosB and CaMKIIα both regulate AMPA glutamate receptor expression and function in NAc, dendritic spine formation on NAc medium spiny neurons (MSNs), and locomotor sensitization to cocaine, no direct link between these molecules has to date been explored. Here, we demonstrate that Δ FosB is phosphorylated by CaMKIIα at the protein-stabilizing Ser27 and that CaMKII is required for the cocaine-mediated accumulation of Δ FosB in rat NAc. Conversely, we show that ΔFosB is both necessary and sufficient for cocaine induction of CaMKIIα gene expression in vivo, an effect selective for D1-type MSNs in the NAc shell subregion. Furthermore, induction of dendritic spines on NAc MSNs and increased behavioral responsiveness to cocaine after NAc overexpression of Δ FosB are both CaMKII dependent. Importantly, we demonstrate for the first time induction of Δ FosB and CaMKII αin the NAc of human cocaine addicts, suggesting possible targets for future therapeutic intervention. These data establish that Δ FosB and CaMKIIα engage in a cell-type-and brain-region-specific positive feedforward loop as a key mechanism for regulating the reward circuitry of the brain in response to chronic cocaine.

Original languageEnglish (US)
Pages (from-to)4295-4307
Number of pages13
JournalJournal of Neuroscience
Volume33
Issue number10
DOIs
StatePublished - Mar 6 2013

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ASJC Scopus subject areas

  • Neuroscience(all)

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