A Molecular Calcium Integrator Reveals a Striatal Cell Type Driving Aversion
Author(s) -
Christina K. Kim,
Mateo I. Sánchez,
Paul Hoerbelt,
Lief E. Fenno,
Robert C. Malenka,
Karl Deisseroth,
Alice Y. Ting
Publication year - 2020
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2020.11.015
Subject(s) - biology , reprogramming , optogenetics , nucleus accumbens , calcium imaging , population , transcriptome , medium spiny neuron , cell type , microbiology and biotechnology , neuroscience , cell , rna , genetics , gene expression , gene , calcium , dopamine , medicine , striatum , demography , sociology
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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