奶油
转录组
星形胶质细胞
伏隔核
生物
神经科学
中棘神经元
腺苷
细胞生物学
调节器
运动前神经元活动
转录调控
核糖核酸
基因表达
化学
基因表达调控
中枢神经系统
核心
HEK 293细胞
钙显像
作者
Leanne M. Holt,Angélica Minier-Toribio,Rita Futamura,Caleb J. Browne,Freddyson J. Martínez-Rivera,Tamara Markovic,Trevonn Gyles,Szu-Ying Yeh,Eric M. Parise,Matthew J. Rivera,Corrine Brenner,Yun Young Yim,Veronika Kondev,Molly Estill,Shi Yan,Eleanor Keane,Alexa Labanca,G Rojas,Li Shen,Yan Dong
出处
期刊:PubMed
日期:2025-12-19
卷期号:11 (51): eaea2419-eaea2419
标识
DOI:10.1126/sciadv.aea2419
摘要
Emerging evidence increasingly indicates that astrocytes are involved in neuropsychiatric disorders, including addiction, but the cocaine-induced astrocyte transcriptome has yet to be investigated. We performed RNA sequencing on whole-cell sorted astrocytes from the nucleus accumbens and bioinformatically characterized the astrocyte transcriptome following cocaine self-administration in male mice. We found that astrocytes exhibit robust and contextually specific transcriptional signatures that implicate adenosine 3',5'-monophosphate response element-binding protein (CREB) as a cocaine-induced transcriptional regulator in astrocytes. Cleavage under targets and release using nuclease sequencing (CUT&RUN) revealed increased astrocytic CREB DNA binding in response to cocaine. Viral-mediated manipulation of nucleus accumbens astrocytic CREB activity in combination with addiction-related behaviors revealed that astrocytic CREB increases the rewarding and reinforcing properties of cocaine. Furthermore, we identified potential molecular mechanisms of astrocytic CREB's influence through modulating astrocytic calcium dynamics and selectively increasing D1-type medium spiny neuronal activity.
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