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用于深入分析神经元突起RNA含量的轴突测序

Axon-seq for in Depth Analysis of the RNA Content of Neuronal Processes.

作者信息

Nijssen Jik, Aguila Julio, Hedlund Eva

机构信息

Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

Bio Protoc. 2019 Jul 20;9(14):e3312. doi: 10.21769/BioProtoc.3312.

Abstract

Neuronal processes have an RNA composition that is distinct from the cell body. Therefore, to fully understand neuronal biology in health and disease we need to study both somas, dendrites and axons. Here we describe a detailed protocol of a newly refined method, Axon-seq, for RNA sequencing of axons (and dendrites) grown in isolation using single microfluidic devices. We also detail how to generate motor neurons from mouse and human pluripotent stem cells for sequencing, but Axon-seq is applicable to any neuronal cell. In Axon-seq, the axons are recruited through a growth factor gradient, lysed and directly processed to cDNA without RNA isolation. A careful bioinformatic step ensures that any soma-contaminated samples are easily identified and removed.

摘要

神经元突起具有与细胞体不同的RNA组成。因此,为了全面了解健康和疾病状态下的神经元生物学,我们需要同时研究胞体、树突和轴突。在这里,我们描述了一种新改进方法Axon-seq的详细方案,该方法用于对使用单个微流控装置单独培养的轴突(和树突)进行RNA测序。我们还详细介绍了如何从小鼠和人类多能干细胞生成运动神经元用于测序,但Axon-seq适用于任何神经元细胞。在Axon-seq中,轴突通过生长因子梯度被募集,裂解后直接处理成cDNA,无需进行RNA分离。一个仔细的生物信息学步骤可确保任何被胞体污染的样本都能被轻松识别并去除。

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