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An Improved Model for Nucleation-Limited Ice Formation in Living Cells during Freezing

机译:冷冻过程中活细胞中成核受限冰形成的改进模型

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摘要

Ice formation in living cells is a lethal event during freezing and its characterization is important to the development of optimal protocols for not only cryopreservation but also cryotherapy applications. Although the model for probability of ice formation (PIF) in cells developed by Toner et al. has been widely used to predict nucleation-limited intracellular ice formation (IIF), our data of freezing Hela cells suggest that this model could give misleading prediction of PIF when the maximum PIF in cells during freezing is less than 1 (PIF ranges from 0 to 1). We introduce a new model to overcome this problem by incorporating a critical cell volume to modify the Toner's original model. We further reveal that this critical cell volume is dependent on the mechanisms of ice nucleation in cells during freezing, i.e., surface-catalyzed nucleation (SCN) and volume-catalyzed nucleation (VCN). Taken together, the improved PIF model may be valuable for better understanding of the mechanisms of ice nucleation in cells during freezing and more accurate prediction of PIF for cryopreservation and cryotherapy applications.
机译:活细胞中的冰形成是冷冻过程中的致命事件,其特征对于开发不仅适用于冷冻保存而且适用于冷冻疗法的最佳方案也很重要。尽管Toner等人开发了细胞中冰形成概率(PIF)的模型。已广泛用于预测成核受限的细胞内冰形成(IIF),我们的冷冻Hela细胞数据表明,当冷冻过程中细胞中的最大PIF小于1(PIF范围为0至1)。我们引入了一种新模型来解决此问题,方法是合并一个关键的电池盒容积以修改碳粉的原始模型。我们进一步揭示该临界细胞体积取决于冷冻过程中细胞中冰成核的机理,即表面催化成核(SCN)和体积催化成核(VCN)。综上所述,改进的PIF模型可能对于更好地了解冷冻过程中细胞中冰核形成的机制以及为冷冻保存和冷冻疗法应用更准确地预测PIF具有有价值的价值。

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