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成像胞间连丝。

Imaging plasmodesmata.

机构信息

Institute of Molecular Plant Sciences, University of Edinburgh, Mayfield Road, Edinburgh, EH9 3JR, UK.

出版信息

Protoplasma. 2011 Jan;248(1):9-25. doi: 10.1007/s00709-010-0233-6. Epub 2010 Nov 12.

Abstract

At only 50 nm in diameter, plasmodesmata (PD) are below the limit of resolution of conventional light microscopy. Consequently, much of our current interpretation of the substructure of PD is derived from transmission electron microscopy. However, PD can be imaged with alternative techniques, including field emission scanning electron microscopy and 'super-resolution' imaging approaches such as 3D-structured illumination microscopy. This review considers the methods currently available for studying PD and focuses on the boundary between light- and electron-based imaging approaches.

摘要

直径仅 50nm 的胞间连丝(PD)低于传统光学显微镜的分辨率极限。因此,我们目前对 PD 亚结构的大部分解释都来自于透射电子显微镜。然而,PD 可以通过其他技术进行成像,包括场发射扫描电子显微镜和“超分辨率”成像方法,如 3D 结构照明显微镜。本文回顾了目前用于研究 PD 的方法,并重点讨论了基于光和电子的成像方法之间的界限。

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