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利用CellREADR对人类皮层中的RNA可编程细胞类型进行监测与操控。

RNA-programmable cell type monitoring and manipulation in the human cortex with CellREADR.

作者信息

Matthews Elizabeth A, Russ Jeffrey B, Qian Yongjun, Zhao Shengli, Thompson Peyton, Methani Muhib, Vestal Matthew L, Josh Huang Z, Southwell Derek G

机构信息

Department of Neurosurgery, Duke University School of Medicine, Durham, NC USA.

Department of Neurobiology, Duke University School of Medicine, Durham, NC USA.

出版信息

bioRxiv. 2024 Dec 6:2024.12.03.626590. doi: 10.1101/2024.12.03.626590.

DOI:10.1101/2024.12.03.626590
PMID:39677799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11642864/
Abstract

Reliable and systematic experimental access to diverse cell types is necessary for understanding the neural circuit organization, function, and pathophysiology of the human brain. Methods for targeting human neural populations are scarce and currently center around identifying and engineering transcriptional enhancers and viral capsids. Here we demonstrate the utility of CellREADR, a programmable RNA sensor-effector technology that couples cellular RNA sensing to effector protein translation, for accessing, monitoring, and manipulating specific neuron types in human cortical tissues. We designed CellREADR constructs to target two distinct human neuron types, (calretinin) GABAergic interneurons and + (forkhead box protein P2) glutamatergic projection neurons, and validated cell targeting using histological, electrophysiological, and transcriptomic methods. CellREADR-mediated expression of optogenetic effectors and genetically-encoded calcium indicators allowed us to manipulate and monitor these neuronal populations in cortical microcircuits. We further demonstrate that AAV-based CellREADR and enhancer vectors can be jointly used to target different subpopulations in the same preparation. By demonstrating specific, reliable, and programmable experimental access to targeted cell types, our results highlight CellREADR's potential for studying human neural circuits and treating brain disorders with cell type resolution.

摘要

可靠且系统地获取各种细胞类型对于理解人类大脑的神经回路组织、功能及病理生理学至关重要。针对人类神经群体的方法稀缺,目前主要围绕识别和改造转录增强子及病毒衣壳展开。在此,我们展示了CellREADR的实用性,这是一种可编程的RNA传感器 - 效应器技术,它将细胞RNA传感与效应蛋白翻译相结合,用于在人类皮质组织中获取、监测和操纵特定的神经元类型。我们设计了CellREADR构建体来靶向两种不同的人类神经元类型,即钙视网膜蛋白(calretinin)γ - 氨基丁酸能中间神经元和叉头框蛋白P2(forkhead box protein P2)谷氨酸能投射神经元,并使用组织学、电生理学和转录组学方法验证了细胞靶向。CellREADR介导的光遗传学效应器和基因编码钙指示剂的表达使我们能够在皮质微回路中操纵和监测这些神经元群体。我们进一步证明,基于腺相关病毒(AAV)的CellREADR和增强子载体可联合用于在同一制剂中靶向不同的亚群。通过展示对靶向细胞类型的特异性、可靠性和可编程的实验性获取,我们的结果突出了CellREADR在以细胞类型分辨率研究人类神经回路和治疗脑部疾病方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/17267c2f7d3e/nihpp-2024.12.03.626590v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/75352ee54894/nihpp-2024.12.03.626590v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/960aa3d88541/nihpp-2024.12.03.626590v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/4ff41fe8f9e1/nihpp-2024.12.03.626590v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/3c16c6510000/nihpp-2024.12.03.626590v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/17267c2f7d3e/nihpp-2024.12.03.626590v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/75352ee54894/nihpp-2024.12.03.626590v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/960aa3d88541/nihpp-2024.12.03.626590v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/4ff41fe8f9e1/nihpp-2024.12.03.626590v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/3c16c6510000/nihpp-2024.12.03.626590v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a07/12233745/17267c2f7d3e/nihpp-2024.12.03.626590v2-f0005.jpg

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