Nuclear calcium signaling in D1 receptor-expressing neurons of the nucleus accumbens regulates molecular, cellular and behavioral adaptations to cocaine.

IF 9.6 1区 医学 Q1 NEUROSCIENCES Biological Psychiatry Pub Date : 2025-01-24 DOI:10.1016/j.biopsych.2025.01.013
Estefani Saint-Jour, Marie-Charlotte Allichon, Andry Andrianarivelo, Enrica Montalban, Claire Martin, Lisa Huet, Nicolas Heck, Anna M Hagenston, Aisha Ravenhorst, Mélanie Marias, Nicolas Gervasi, Faustine Arrivet, Adèle Vilette, Katleen Pinchaud, Sandrine Betuing, Thomas Lissek, Jocelyne Caboche, Hilmar Bading, Peter Vanhoutte
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Abstract

Background: The persistence of cocaine-evoked adaptations relies on gene regulations within the reward circuit, especially in the ventral striatum (i.e., nucleus accumbens (NAc)). Notably, activation of the extracellular signal-regulated kinase (ERK) pathway in the striatum is known to trigger a transcriptional program shaping long-term responses to cocaine. Nuclear calcium signaling has also been shown to control multiple forms of transcription-dependent neuroadaptations but the dynamics and roles of striatal nuclear calcium signaling in preclinical models of addiction remains unknown.

Methods: A genetically-encoded cell-type-specific nuclear calcium probe has been developed to monitor calcium dynamics in the nuclei of striatal neurons, including in freely-moving mice. A cell-type-specific inhibitor of nuclear calcium signaling, combined with 3D imaging of neuronal morphology, immunostaining and behavior, was used to disentangle the roles of nuclear calcium in NAc medium-sized spiny neurons (MSN) expressing the dopamine D1 (D1R) or D2 (D2R) receptor on cocaine-evoked responses.

Results: The D1R-mediated potentiation of calcium influx through glutamate N-methyl-D-aspartate receptors (NMDAR), which shapes cocaine effects, also drives nuclear calcium transients. Fiber photometry revealed that cocaine-treated mice display a sustained nuclear calcium increase in NAc D1R-MSN. Disrupting nuclear calcium in D1R-MSN, but not D2R-MSN, blocks cocaine-evoked morphological changes of MSN and gene expression, and blunts cocaine's rewarding effects.

Conclusions: Our study unravels the dynamics and roles of cocaine-induced nuclear calcium signaling increases in D1R-MSN on molecular, cellular and behavioral adaptations to cocaine, and brings a significant breakthrough as it could contribute to the development of innovative strategies with therapeutic potential to alleviate addiction symptoms.

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背景:可卡因诱发适应的持续性依赖于奖赏回路中的基因调控,尤其是在腹侧纹状体(即伏隔核(NAc))中。值得注意的是,已知纹状体中细胞外信号调节激酶(ERK)通路的激活会触发转录程序,形成对可卡因的长期反应。核钙信号也被证明能控制多种形式的转录依赖性神经适应,但临床前成瘾模型中纹状体核钙信号的动态和作用仍不清楚:方法:已开发出一种基因编码的细胞类型特异性核钙探针,用于监测纹状体神经元核内的钙动态,包括在自由活动的小鼠体内。一种细胞类型特异的核钙信号转导抑制剂与神经元形态、免疫染色和行为的三维成像相结合,被用来区分表达多巴胺D1(D1R)或D2(D2R)受体的NAc中型棘神经元(MSN)中的核钙对可卡因诱发反应的作用:结果:D1R介导的钙离子通过谷氨酸N-甲基-D-天冬氨酸受体(NMDAR)流入的增效作用也驱动了核钙离子瞬态。纤维光度法显示,可卡因处理过的小鼠在 NAc D1R-MSN 中显示出持续的核钙质增加。干扰D1R-MSN(而非D2R-MSN)的核钙可阻断可卡因诱发的MSN形态变化和基因表达,并减弱可卡因的奖赏效应:我们的研究揭示了可卡因诱导的D1R-MSN核钙化信号增加对可卡因的分子、细胞和行为适应的动态变化和作用,是一项重大突破,有助于开发具有治疗潜力的创新策略,缓解成瘾症状。
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来源期刊
Biological Psychiatry
Biological Psychiatry 医学-精神病学
CiteScore
18.80
自引率
2.80%
发文量
1398
审稿时长
33 days
期刊介绍: Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.
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