Prosapip1-Dependent Synaptic Adaptations in the Nucleus Accumbens Drive Alcohol Intake, Seeking, and Reward.
Prosapip1-Dependent Synaptic Adaptations in the Nucleus Accumbens Drive Alcohol Intake, Seeking, and Reward.
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DOI:
10.1016/j.neuron.2017.08.037
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发表时间:
2017-09-27
期刊:
影响因子:
16.2
通讯作者:
Ron D
中科院分区:
文献类型:
--
作者:
Laguesse S;Morisot N;Shin JH;Liu F;Adrover MF;Sakhai SA;Lopez MF;Phamluong K;Griffin WC 3rd;Becker HC;Bender KJ;Alvarez VA;Ron D
The mammalian target of rapamycin complex 1 (mTORC1), a transducer of local dendritic translation, participates in learning and memory processes as well as in mechanisms underlying alcohol-drinking behaviors. Using an unbiased RNA-seq approach, we identified Prosapip1 as a novel downstream target of mTORC1 whose translation and consequent synaptic protein expression are increased in the nucleus accumbens (NAc) of mice excessively consuming alcohol. We demonstrate that alcohol-dependent increases in Prosapip1 levels promote the formation of actin filaments, leading to changes in dendritic spine morphology of NAc medium spiny neurons (MSNs). We further demonstrate that Prosapip1 is required for alcohol-dependent synaptic localization of GluA2 lacking AMPA receptors in NAc shell MSNs. Finally, we present data implicating Prosapip1 in mechanisms underlying alcohol self-administration and reward. Together, these data suggest that Prosapip1 in the NAc is a molecular transducer of structural and synaptic alterations that drive and/or maintain excessive alcohol use. Laguesse et al. identified Prosapip1 as a novel downstream target of mTORC1 in the nucleus accumbens that promotes actin reorganization as well as morphological and synaptic alterations that in turn drive alcohol drinking and seeking behaviors.
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