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通过对内化分子的亚衍射跟踪,可视化活神经元中的内吞作用再循环和转运。

Visualizing endocytic recycling and trafficking in live neurons by subdiffractional tracking of internalized molecules.

机构信息

Clem Jones Centre for Ageing Dementia Research, The University of Queensland, Brisbane, Queensland, Australia.

Queensland Brain Institute, The University of Queensland, Brisbane, Queensland, Australia.

出版信息

Nat Protoc. 2017 Dec;12(12):2590-2622. doi: 10.1038/nprot.2017.116. Epub 2017 Nov 30.

Abstract

Our understanding of endocytic pathway dynamics is restricted by the diffraction limit of light microscopy. Although super-resolution techniques can overcome this issue, highly crowded cellular environments, such as nerve terminals, can also dramatically limit the tracking of multiple endocytic vesicles such as synaptic vesicles (SVs), which in turn restricts the analytical dissection of their discrete diffusional and transport states. We recently introduced a pulse-chase technique for subdiffractional tracking of internalized molecules (sdTIM) that allows the visualization of fluorescently tagged molecules trapped in individual signaling endosomes and SVs in presynapses or axons with 30- to 50-nm localization precision. We originally developed this approach for tracking single molecules of botulinum neurotoxin type A, which undergoes activity-dependent internalization and retrograde transport in autophagosomes. This method was then adapted to localize the signaling endosomes containing cholera toxin subunit-B that undergo retrograde transport in axons and to track SVs in the crowded environment of hippocampal presynapses. We describe (i) the construction of a custom-made microfluidic device that enables control over neuronal orientation; (ii) the 3D printing of a perfusion system for sdTIM experiments performed on glass-bottom dishes; (iii) the dissection, culturing and transfection of hippocampal neurons in microfluidic devices; and (iv) guidance on how to perform the pulse-chase experiments and data analysis. In addition, we describe the use of single-molecule-tracking analytical tools to reveal the average and the heterogeneous single-molecule mobility behaviors. We also discuss alternative reagents and equipment that can, in principle, be used for sdTIM experiments and describe how to adapt sdTIM to image nanocluster formation and/or tubulation in early endosomes during sorting events. The procedures described in this protocol take ∼1 week.

摘要

我们对胞吞作用途径动态的理解受到光显微镜的衍射极限的限制。虽然超分辨率技术可以克服这个问题,但高度拥挤的细胞环境,如神经末梢,也可以极大地限制对多个胞吞小泡(如突触小泡(SVs))的跟踪,这反过来又限制了对其离散扩散和运输状态的分析。我们最近引入了一种用于亚衍射追踪内化分子(sdTIM)的脉冲追踪技术,该技术允许用 30-50nm 的定位精度可视化荧光标记的分子被困在单个信号内体和突触前或轴突中的 SVs 中。我们最初开发这种方法是为了追踪肉毒杆菌神经毒素 A 型的单个分子,该分子在自噬体中经历依赖于活性的内化和逆行运输。然后,该方法被改编用于定位含有霍乱毒素亚基-B 的信号内体,该内体在轴突中经历逆行运输,并追踪海马突触前拥挤环境中的 SVs。我们描述了(i)构建一个定制的微流控装置,该装置能够控制神经元的方向;(ii)用于在玻璃底培养皿上进行 sdTIM 实验的 3D 打印灌注系统;(iii)在微流控装置中分离、培养和转染海马神经元;以及(iv)进行脉冲追踪实验和数据分析的指导。此外,我们描述了使用单分子跟踪分析工具来揭示平均和异质单分子迁移行为。我们还讨论了可以用于 sdTIM 实验的替代试剂和设备,并描述了如何将 sdTIM 用于在分选事件中成像早期内体中的纳米簇形成和/或小管化。本方案中描述的程序大约需要 1 周时间。

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