Graduate School of Science and Engineering, Department of Regulation-Biology, Faculty of Science, Saitama University, 255 Shimo-Okubo, Sakura-ku, Saitama City, Saitama 338-8570, Japan.
Planta. 2010 Mar;231(4):965-76. doi: 10.1007/s00425-010-1101-5. Epub 2010 Jan 26.
Some cultured plant cells are able to acquire tolerance to various stresses when they are cultured under suitably controlled conditions. Induction of a high level of desiccation tolerance in suspension-cultured cells of the liverwort Marchantia polymorpha was examined for studying the mechanisms of desiccation tolerance and vitrification at the cellular level. Desiccation tolerance level of cells was very low and the survival rate was less than 10% after exposure to drying below 0.1 g H(2)O g(-1) dry weight (DW). Preculture treatment in 0.5 M sucrose medium was the most effective method for inducing a high level of desiccation tolerance in cells and the survival rate was 87% even after being desiccated to below 0.1 g H(2)O g(-1) DW. Preculture treatment caused alteration of cell structures and accumulation of a large amount of sucrose and newly synthesized proteins in cells. Abundant sucrose and preculture-induced proteins were necessary for full development of desiccation tolerance in the cells. When water content decreased to below 0.1 g H(2)O g(-1) DW, desiccation-tolerant cells that had been precultured were vitrified above 0 degrees C and maintained stable viability. We have succeeded in the induction of desiccation tolerance that allows formation of intracellular glass with cell viability at ambient temperatures by controlling culture conditions, and our results suggest that suspension-cultured cells of M. polymorpha are useful for studying cellular mechanisms for the development of desiccation tolerance and the stabilization of vitrified cells.
在适当控制条件下培养时,一些培养的植物细胞能够获得对各种胁迫的耐受能力。为了研究细胞水平脱水耐性和玻璃化的机制,我们研究了悬浮培养的地钱(Marchantia polymorpha)细胞获得高水平脱水耐性的诱导。细胞的脱水耐性水平很低,在暴露于低于 0.1 g H2O g(-1)干重(DW)的干燥条件下,存活率不到 10%。在 0.5 M 蔗糖培养基中的预培养处理是诱导细胞高水平脱水耐性的最有效方法,即使在干燥至低于 0.1 g H2O g(-1) DW 时,存活率仍为 87%。预培养处理导致细胞结构的改变和大量蔗糖和新合成蛋白质的积累。大量的蔗糖和预培养诱导的蛋白质是细胞充分发展脱水耐性所必需的。当水含量下降至低于 0.1 g H2O g(-1) DW 时,经过预培养的耐脱水细胞在 0 度以上玻璃化,并保持稳定的活力。通过控制培养条件,我们成功地诱导了允许在环境温度下形成具有细胞活力的细胞内玻璃的脱水耐性,我们的结果表明,悬浮培养的地钱细胞可用于研究发展脱水耐性和稳定玻璃化细胞的细胞机制。