TY - JOUR
T1 - 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
AU - Robison, Alfred J.
AU - Vialou, Vincent
AU - Mazei-Robison, Michelle
AU - Feng, Jian
AU - Kourrich, Saïd
AU - Collins, Miles
AU - Wee, Sunmee
AU - Koob, George
AU - Turecki, Gustavo
AU - Neve, Rachael
AU - Thomas, Mark
AU - Nestler, Eric J.
PY - 2013/3/6
Y1 - 2013/3/6
N2 - 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.
AB - 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.
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U2 - 10.1523/JNEUROSCI.5192-12.2013
DO - 10.1523/JNEUROSCI.5192-12.2013
M3 - Article
C2 - 23467346
AN - SCOPUS:84874627808
SN - 0270-6474
VL - 33
SP - 4295
EP - 4307
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 10
ER -