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可视化和量化培养神经元中的细胞器轴突运输。

Visualization and Quantification of Organelle Axonal Transport in Cultured Neurons.

机构信息

Department of Physiology and Pennsylvania Muscle Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Methods Mol Biol. 2024;2831:219-234. doi: 10.1007/978-1-0716-3969-6_15.

Abstract

The specialized function and extreme geometry of neurons necessitates a unique reliance upon long-distance microtubule-based transport. Appropriate trafficking of axonal cargos by motor proteins is essential for establishing circuitry during development and continuing function throughout a lifespan. Visualizing and quantifying cargo movement provides valuable insight into how axonal organelles are replenished, recycled, and degraded during the dynamic dance of outgoing and incoming axonal traffic. Long-distance axonal trafficking is of particular importance as it encompasses a pathway commonly disrupted in developmental and degenerative disease states. Here, we describe neuronal organelles and outline methods for live imaging and quantifying their movement throughout the axon via transient expression of fluorescently labeled organelle markers. This resource provides recommendations for target proteins/domains and appropriate acquisition time scales for visualizing distinct neuronal cargos in cultured neurons derived from human induced pluripotent stem cells (iPSCs) and primary rat neurons.

摘要

神经元的特殊功能和极端几何形状需要独特地依赖长距离基于微管的运输。运动蛋白适当运输轴突货物对于在发育过程中建立回路以及在整个生命周期中保持功能至关重要。对货物运动进行可视化和定量分析,可深入了解轴突细胞器在进出轴突交通的动态舞蹈中如何得到补充、再循环和降解。长距离轴突运输尤为重要,因为它包含在发育和退行性疾病状态中通常受到破坏的途径。在这里,我们描述了神经元细胞器,并概述了通过瞬时表达荧光标记细胞器标记物在整个轴突中对其进行活细胞成像和定量分析的方法。本资源针对目标蛋白/结构域提供了建议,并针对来自人诱导多能干细胞(iPSC)和原代大鼠神经元的培养神经元中可视化不同神经元货物的适当采集时间尺度提供了建议。

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