Effect of the successive steps of a cryopreservation protocol on the structural integrity of Rubia akane Nakai hairy roots

2014

Article référencé dans le Web of Science WOS:000335159300018

Salma M., Sylvestre Isabelle, Collin Myriam, Escoute J., Lartaud M., Yi J. Y., Kim H. H., Verdeil J. L., Engelmann Florent

Protoplasma, 2014, 251 (3), p. 649-659 ISSN 0033-183X

In this work, we studied the impact of the successive steps of the droplet-vitrification protocol technique employed for cryopreservation of Rubia akane hairy roots on the features of cortical, pericycle and endoderm cells of apical and central root segments, using histology techniques and combining qualitative and quantitative observations. In apical segments, plasmolysis (22-71 %, depending on cell type) was observed only after the loading treatment and did not increase after the following steps of the protocol. By contrast, in central segments, plasmolysis (39-45 %) was already observed after the sucrose pretreatment; it increased to 54-68 %, depending on cell type, after the loading treatment, but no further changes were noted after treatment with the vitrification solution. After liquid nitrogen exposure and unloading treatment, deplasmolysis was more rapid in apical segments, with cortical and pericycle cells having retrieved their original features. In central segments, only cortical cells had retrieved their original features and endoderm and pericycle cells were still highly plasmolysed. Nuclei were more strongly impacted by the cryopreservation protocol in central segments, where they displayed a highly condensed nucleoplasm from the loading treatment onwards and had not retrieved their original aspect after the unloading treatment. By contrast, nuclei had a much less condensed nucleoplasm in cells of apical segments, and they had retrieved their original aspect after the unloading treatment.

Sciences du monde végétal [076] ; Biotechnologies [084]

Fonds IRD [F B010061998]

fdi:010061998