生物
重编程
光遗传学
伏隔核
人口
钙显像
转录组
细胞生物学
神经科学
中棘神经元
电池类型
细胞
遗传学
基因表达
基因
钙
多巴胺
基底神经节
内科学
人口学
中枢神经系统
社会学
医学
作者
Christina K. Kim,Mateo I. Sánchez,Paul Hoerbelt,Lief E. Fenno,Robert C. Malenka,Karl Deisseroth,Alice Y. Ting
出处
期刊:Cell
[Cell Press]
日期:2020-12-01
卷期号:183 (7): 2003-2019.e16
被引量:36
标识
DOI:10.1016/j.cell.2020.11.015
摘要
The ability to record transient cellular events in the DNA or RNA of cells would enable precise, large-scale analysis, selection, and reprogramming of heterogeneous cell populations. Here, we report a molecular technology for stable genetic tagging of cells that exhibit activity-related increases in intracellular calcium concentration (FLiCRE). We used FLiCRE to transcriptionally label activated neural ensembles in the nucleus accumbens of the mouse brain during brief stimulation of aversive inputs. Using single-cell RNA sequencing, we detected FLiCRE transcripts among the endogenous transcriptome, providing simultaneous readout of both cell-type and calcium activation history. We identified a cell type in the nucleus accumbens activated downstream of long-range excitatory projections. Taking advantage of FLiCRE’s modular design, we expressed an optogenetic channel selectively in this cell type and showed that direct recruitment of this otherwise genetically inaccessible population elicits behavioral aversion. The specificity and minute resolution of FLiCRE enables molecularly informed characterization, manipulation, and reprogramming of activated cellular ensembles.
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