Literature DB >> 35349132

Plasmodesmata Ultrastructure Determination Using Electron Tomography.

Jules D Petit1,2, Marie Glavier1, Lysiane Brocard3, Emmanuelle M F Bayer4.   

Abstract

Plant plasmodesmata (PD) are complex intercellular channels consisting of a thin endoplasmic reticulum (ER) tubule enveloped by the plasma membrane (PM). PD were first observed by electron microscopy about 50 years ago and, since, numerous studies in transmission and scanning electron microscopy have provided important information regarding their overall organization, revealing at the same time their diversity in terms of structure and morphology. However, and despite the fact that PD cell-cell communication is of critical importance for plant growth, development, cellular patterning, and response to biotic and abiotic stresses, linking their structural organization to their functional state has been proven difficult. This is in part due to their small size (20-50 nm in diameter) and the difficulty to resolve these structures in three dimensions at nanometer resolution to provide details of their internal organization.In this protocol, we provide in detail a complete process to produce high-resolution transmission electron tomograms of PD. We describe the preparation of the plant sample using high-pressure cryofixation and cryo-substitution. We also describe how to prepare filmed grids and how to cut and collect the sections using an ultramicrotome. We explain how to acquire a tilt series and how to reconstruct a tomogram from it using the IMOD software. We also give a few guidelines on segmentation of the reconstructed tomogram.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Cryofixation; Electron tomography; Plasmodesmata; Segmentation; Ultrastructure

Mesh:

Year:  2022        PMID: 35349132     DOI: 10.1007/978-1-0716-2132-5_3

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

Review 1.  Imaging plasmodesmata.

Authors:  Karen Bell; Karl Oparka
Journal:  Protoplasma       Date:  2010-11-12       Impact factor: 3.356

2.  High resolution scanning electron microscopy of plasmodesmata.

Authors:  Sarah Brecknock; Teresa P Dibbayawan; Maret Vesk; Peter A Vesk; Christine Faulkner; Deborah A Barton; Robyn L Overall
Journal:  Planta       Date:  2011-05-28       Impact factor: 4.116

3.  Computer visualization of three-dimensional image data using IMOD.

Authors:  J R Kremer; D N Mastronarde; J R McIntosh
Journal:  J Struct Biol       Date:  1996 Jan-Feb       Impact factor: 2.867

4.  Architecture and permeability of post-cytokinesis plasmodesmata lacking cytoplasmic sleeves.

Authors:  William J Nicolas; Magali S Grison; Sylvain Trépout; Amélia Gaston; Mathieu Fouché; Fabrice P Cordelières; Karl Oparka; Jens Tilsner; Lysiane Brocard; Emmanuelle M Bayer
Journal:  Nat Plants       Date:  2017-06-12       Impact factor: 15.793

Review 5.  Cryo-electron microscopy for the study of virus assembly.

Authors:  Daniel Luque; José R Castón
Journal:  Nat Chem Biol       Date:  2020-02-20       Impact factor: 15.040

Review 6.  Advances in the field of single-particle cryo-electron microscopy over the last decade.

Authors:  Joachim Frank
Journal:  Nat Protoc       Date:  2017-01-05       Impact factor: 13.491

7.  Electron Tomography to Study the Three-dimensional Structure of Plasmodesmata in Plant Tissues-from High Pressure Freezing Preparation to Ultrathin Section Collection.

Authors:  William J Nicolas; Emmanuelle Bayer; Lysiane Brocard
Journal:  Bio Protoc       Date:  2018-01-05
  7 in total

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