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A protocol for combining fluorescent proteins with histological stains for diverse cell wall components
Author(s) -
Ursache Robertas,
Andersen Tonni Grube,
Marhavý Peter,
Geldner Niko
Publication year - 2018
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1111/tpj.13784
Subject(s) - biology , autofluorescence , fluorescence , clearance , staining , protein subcellular localization prediction , microbiology and biotechnology , computational biology , green fluorescent protein , plant cell , cell wall , biophysics , biochemistry , gene , genetics , physics , quantum mechanics , medicine , urology
Summary Higher plant function is contingent upon the complex three‐dimensional (3D) architecture of plant tissues, yet severe light scattering renders deep, 3D tissue imaging very problematic. Although efforts to ‘clear’ tissues have been ongoing for over a century, many innovations have been made in recent years. Among them, a protocol called ClearSee efficiently clears tissues and diminishes chlorophyll autofluorescence while maintaining fluorescent proteins – thereby allowing analysis of gene expression and protein localisation in cleared samples. To further increase the usefulness of this protocol, we have developed a ClearSee‐based toolbox in which a number of classical histological stains for lignin, suberin and other cell wall components can be used in conjunction with fluorescent reporter lines. We found that a number of classical dyes are highly soluble in ClearSee solution, allowing the old staining protocols to be enormously simplified; these additionally have been unsuitable for co‐visualisation with fluorescent markers due to harsh fixation and clearing. Consecutive staining with several dyes allows 3D co‐visualisation of distinct cell wall modifications with fluorescent proteins – used as transcriptional reporters or protein localisation tools – deep within tissues. Moreover, the protocol is easily applied on hand sections of different organs. In combination with confocal microscopy, this improves image quality while decreasing the time and cost of embedding/sectioning. It thus provides a low‐cost, efficient method for studying thick plant tissues which are usually cumbersome to visualise. Our ClearSee‐adapted protocols significantly improve and speed up anatomical and developmental investigations in numerous plant species, and we hope they will contribute to new discoveries in many areas of plant research.