improved method for clearing and staining free-hand sections and whole-mount samples

• Published in: Annals of botany 2005-11, Vol.96 (6), p.989-996
• Main Authors: Lux, A, Morita, S, Abe, J, Ito, K
• Format: Article
• Language: English
• Subjects: Allium cepa; Camellia sinensis; Casparian bands; Cell Wall; Cell walls; clearing; Corn; cucumbers; Cucumis melo; Cucumis sativus; differential staining; Endodermis; Epidermal cells; exodermis; Fluorescence; fluorescence emission spectroscopy; fluorescence microscopy; grain sorghum; Hand sections; Laboratory staining techniques; melons; methodology; Microscopy; Microscopy, Fluorescence - methods; Microtomy - methods; Oncidium; onions; Original; plant anatomy; Plant roots; Plant Roots - anatomy & histology; Plant Roots - cytology; Plants; roots; Sorghum; Sorghum bicolor; Specimen Handling; Staining and Labeling - methods; tea
• ISSN: 0305-7364; 1095-8290
• DOI: 10.1093/aob/mci266

BACKGROUND AND AIMS: Free-hand sectioning of living plant tissues allows fast microscopic observation of internal structures. The aim of this study was to improve the quality of preparations from roots with suberized cell walls. A whole-mount procedure that enables visualization of exo- and endodermal cells along the root axis was also established. METHODS: Free-hand sections were cleared with lactic acid saturated with chloral hydrate, and observed with or without post-staining in toluidine blue O or aniline blue. Both white light and UV light were used for observation. Lactic acid was also used as a solvent for berberine, and fluorol yellow for clearing and staining the samples used for suberin observation. This procedure was also applied to whole-mount roots with suberized celllayers. KEY RESULTS: Clearing of sections results in good image quality to observe the tissue structure and cell walls compared with non-cleared sections. The use of lactic acid as a solvent for fluorol yellow proved superior to previously used solvents such as polyethylene glycol-glycerol. Clearing and fluorescence staining of thin roots such as those of Arabidopsis thaliana were succesful for suberin visualization in endodermal cells within whole-mount roots. For thicker roots, such as those of maize, sorghum or tea, this procedure could be used for visualizing the exodermis in a longitudinal view. Clearing and staining of peeled maize root segments enabled observation of endodermal cell walls. CONCLUSIONS: The clearing procedure using lactic acid improves the quality of images from free-hand sections and clearings. This method enhaces the study of plant root anatomy, in particular the histological development and changes of cell walls, when used in combination with fluorescence microscopy.