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Publication : Proteasome phosphorylation regulates cocaine-induced sensitization.

First Author  Gonzales FR Year  2018
Journal  Mol Cell Neurosci Volume  88
Pages  62-69 PubMed ID  29217409
Mgi Jnum  J:260973 Mgi Id  MGI:6151972
Doi  10.1016/j.mcn.2017.12.001 Citation  Gonzales FR, et al. (2018) Proteasome phosphorylation regulates cocaine-induced sensitization. Mol Cell Neurosci 88:62-69
abstractText  Repeated exposure to cocaine produces structural and functional modifications at synapses from neurons in several brain regions including the nucleus accumbens. These changes are thought to underlie cocaine-induced sensitization. The ubiquitin proteasome system plays a crucial role in the remodeling of synapses and has recently been implicated in addiction-related behavior. The ATPase Rpt6 subunit of the 26S proteasome is phosphorylated by Ca(2+)/calmodulin-dependent protein kinases II alpha at ser120 which is thought to regulate proteasome activity and distribution in neurons. Here, we demonstrate that Rpt6 phosphorylation is involved in cocaine-induced locomotor sensitization. Cocaine concomitantly increases proteasome activity and Rpt6 S120 phosphorylation in cultured neurons and in various brain regions of wild type mice including the nucleus accumbens and prefrontal cortex. In contrast, cocaine does not increase proteasome activity in Rpt6 phospho-mimetic (ser120Asp) mice. Strikingly, we found a complete absence of cocaine-induced locomotor sensitization in the Rpt6 ser120Asp mice. Together, these findings suggest a critical role for Rpt6 phosphorylation and proteasome function in the regulation cocaine-induced behavioral plasticity.
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