High-throughput cryopreservation of plant cell cultures for functional genomics

• Published in: Plant and cell physiology Vol. 53; no. 5; pp. 943 - 952
• Main Authors: Ogawa, Yoichi, Sakurai, Nozomu, Oikawa, Akira, Kai, Kosuke, Morishita, Yoshihiko, Mori, Kumiko, Moriya, Kanami, Fujii, Fumiko, Aoki, Koh, Suzuki, Hideyuki, Ohta, Daisaku, Saito, Kazuki, Shibata, Daisuke
• Format: Journal Article
• Language: English
• Published: Japan Oxford University Press 01.05.2012
• Subjects: Arabidopsis - cytology; Arabidopsis - genetics; Arabidopsis - physiology; Arabidopsis thaliana; Cell culture; Cell Culture Techniques - methods; Cell Line; Cell Survival - drug effects; Cryopreservation; Cryopreservation - methods; Cryoprotective Agents - pharmacology; Daucus carota; Freezing; Gene expression; Gene Expression Regulation, Plant - drug effects; Genetic engineering; genomics; Genomics - methods; Glucuronidase - metabolism; Glycerol; High-Throughput Screening Assays - methods; Lotus japonicus; Metabolism; Nicotiana tabacum; Nitrogen; Oryza sativa; Plant cells; Plant Cells - drug effects; Plant Cells - metabolism; polystyrene; Proline; Proline - pharmacology; Sucrose; Techniques; Temperature effects
• ISSN: 0032-0781; 1471-9053
• DOI: 10.1093/pcp/pcs038

Suspension-cultured cell lines from plant species are useful for genetic engineering. However, maintenance of these lines is laborious, involves routine subculturing and hampers wider use of transgenic lines, especially when many lines are required for a high-throughput functional genomics application. Cryopreservation of these lines may reduce the need for subculturing. Here, we established a simple protocol for cryopreservation of cell lines from five commonly used plant species, Arabidopsis thaliana, Daucus carota, Lotus japonicus, Nicotiana tabacum and Oryza sativa. The LSP solution (2 M glycerol, 0.4 M sucrose and 86.9 mM proline) protected cells from damage during freezing and was only mildly toxic to cells kept at room temperature for at least 2 h. More than 100 samples were processed for freezing simultaneously. Initially, we determined the conditions for cryopreservation using a programmable freezer; we then developed a modified simple protocol that did not require a programmable freezer. In the simple protocol, a thick expanded polystyrene (EPS) container containing the vials with the cell-LSP solution mixtures was kept at -30 °C for 6 h to cool the cells slowly (pre-freezing); samples from the EPS containers were then plunged into liquid nitrogen before long-term storage. Transgenic Arabidopsis cells were subjected to cryopreservation, thawed and then re-grown in culture; transcriptome and metabolome analyses indicated that there was no significant difference in gene expression or metabolism between cryopreserved cells and control cells. The simplicity of the protocol will accelerate the pace of research in functional plant genomics.