Suppr超能文献

一种分子钙整合器揭示了一种驱动厌恶的纹状体细胞类型。

A Molecular Calcium Integrator Reveals a Striatal Cell Type Driving Aversion.

机构信息

Department of Genetics, Stanford University, Stanford, CA 94305, USA.

Department of Genetics, Stanford University, Stanford, CA 94305, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.

出版信息

Cell. 2020 Dec 23;183(7):2003-2019.e16. doi: 10.1016/j.cell.2020.11.015. Epub 2020 Dec 11.

Abstract

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.

摘要

能够在细胞的 DNA 或 RNA 中记录瞬时细胞事件,将使对异质细胞群体进行精确的、大规模的分析、选择和重编程成为可能。在这里,我们报告了一种用于稳定遗传标记细胞的分子技术,这些细胞表现出与细胞内钙浓度增加相关的活性(FLiCRE)。我们使用 FLiCRE 在对厌恶输入进行短暂刺激期间,对小鼠大脑伏隔核中的激活神经簇进行转录标记。使用单细胞 RNA 测序,我们在内源性转录组中检测到了 FLiCRE 转录本,同时提供了细胞类型和钙激活历史的直接读出。我们在伏隔核中鉴定出一种细胞类型,该细胞类型被长程兴奋性投射激活。利用 FLiCRE 的模块化设计,我们在这种细胞类型中选择性地表达了一种光遗传学通道,并表明直接招募这种在遗传上无法接近的群体可引起行为厌恶。FLiCRE 的特异性和微小分辨率使激活细胞群的分子信息特征分析、操作和重编程成为可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91f6/9839359/30356be51b4a/nihms-1646305-f0002.jpg

相似文献

引用本文的文献

1
Aligning brain and behavior.使大脑与行为相匹配。
Curr Opin Behav Sci. 2025 Apr;62. doi: 10.1016/j.cobeha.2025.101487. Epub 2025 Mar 5.
3
An improved FLARE system for recording and manipulating neuronal activity.一种用于记录和操纵神经元活动的改进型FLARE系统。
Cell Rep Methods. 2025 Apr 21;5(4):101012. doi: 10.1016/j.crmeth.2025.101012. Epub 2025 Mar 21.
5
Protein Engineering for Spatiotemporally Resolved Cellular Monitoring.用于时空分辨细胞监测的蛋白质工程
Annu Rev Anal Chem (Palo Alto Calif). 2025 May;18(1):217-240. doi: 10.1146/annurev-anchem-070124-035857. Epub 2025 Feb 25.
10
DNA Methylation in Long-Term Memory.长期记忆中的DNA甲基化
Physiology (Bethesda). 2025 Jul 1;40(4):0. doi: 10.1152/physiol.00032.2024. Epub 2025 Feb 5.

本文引用的文献

3
Connect-seq to superimpose molecular on anatomical neural circuit maps.Connect-seq 可将分子与解剖神经回路图谱叠加。
Proc Natl Acad Sci U S A. 2020 Feb 25;117(8):4375-4384. doi: 10.1073/pnas.1912176117. Epub 2020 Feb 7.
5
Directed evolution improves the catalytic efficiency of TEV protease.定向进化提高 TEV 蛋白酶的催化效率。
Nat Methods. 2020 Feb;17(2):167-174. doi: 10.1038/s41592-019-0665-7. Epub 2019 Dec 9.
6
Continuous and Discrete Neuron Types of the Adult Murine Striatum.成年鼠纹状体的连续和离散神经元类型。
Neuron. 2020 Feb 19;105(4):688-699.e8. doi: 10.1016/j.neuron.2019.11.004. Epub 2019 Dec 5.
8
Cortical layer-specific critical dynamics triggering perception.皮层层特异性关键动力学触发感知。
Science. 2019 Aug 9;365(6453). doi: 10.1126/science.aaw5202. Epub 2019 Jul 18.
10
Comprehensive Integration of Single-Cell Data.单细胞数据的综合整合。
Cell. 2019 Jun 13;177(7):1888-1902.e21. doi: 10.1016/j.cell.2019.05.031. Epub 2019 Jun 6.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验