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Freeze-substitution transmission electron microscopy of gentian shoot tips cryopreserved at ultra low temperatures

机译:在超低温下冷冻保存的龙胆芽尖的冷冻-替代透射电镜

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摘要

Transmission electron microscopy (TEM) combined with freeze substitution was employed to examine the ultrastructure of cells of gentian shoot tips cooled to the ultra-low temperature of slush nitrogen and liquid nitrogen. When shoot tips were cooled in ultra-low temperature without plant vitrification solution 2 (PVS2) treatment, massive ice formation was observed throughout the cells, indicating that severe injury occurred during cooling. In contrast, when shoot tips were treated with PVS2 and subsequently cooled to ultra- low temperatures, no ice crystals were observed in the cells. In addition, the cells of PVS2-treated shoot tips exhibited considerable plasmolysis and formation of small vesicles in cytoplasm. These results clearly demonstrate that the PVS2 treatment is essential for preventing damage caused by ice formation and for successful cryopreservation of plant shoot tips.
机译:采用透射电子显微镜(TEM)结合冷冻替代法研究了冷却至泥浆氮和液氮超低温的龙胆芽尖细胞的超微结构。当芽尖在未进行植物玻璃化溶液2(PVS2)处理的情况下以超低温冷却时,在整个细胞中均观察到大量的冰形成,表明在冷却过程中发生了严重伤害。相反,当用PVS2处理芽尖并随后冷却至超低温时,在细胞中未观察到冰晶。此外,PVS2处理的芽尖细胞表现出可观的溶酶作用并在细胞质中形成小囊泡。这些结果清楚地表明,PVS2处理对于防止因结冰而造成的损害以及成功地对植物梢进行冷冻保存至关重要。

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