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Modification of cellular membranes conveys cryoprotection to cells during rapid, non-equilibrium cryopreservation

机译:细胞膜的改性在快速,非平衡冷冻保存期间传送到细胞的冷冻保护

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摘要

Rapid cooling and re-warming has been shown promising to cryopreserve living cells, which cannot be preserved by conventional slow freezing methods. However, success is limited by the cytotoxicity of highly concentrated cryoprotective agents. Recent results have shown that cryoprotective agents do not need to suppress intracellular ice crystals completely to allow for survival after cryopreservation. Cryoprotective agents like DMSO or ethylene glycol can also lead to a tolerance of cells towards intracellular ice. It is however unclear by which mechanism this tolerance is achieved. These substances are also known to modulate properties of cellular membranes. It is shown here that cryoprotective DMSO and ethylene glycol have a clear influence on the mobility of lipids in the plasma membrane of HeLa cells. To isolate changes of the properties of plasma membranes from effects on ice formation, the membrane properties were modulated in absence of cryoprotective agents. This was achieved by changing their sterol content. In cells with elevated sterol content, an immobile lipid fraction was present, similar to cells treated with DMSO and ethylene glycol. These cells showed also significantly increased plasma membrane integrity after rapid freezing and thawing in the absence of classical cryoprotective agents. However, their intracellular lysosomes, which cannot be enriched with sterols, still got ruptured. These results clearly indicate that a modulation of membrane properties can convey cryoprotection. Upon slow cooling, elevated sterol content had actually an adverse effect on the plasma membranes, which shows that this effect is specific for rapid, non-equilibrium cooling processes. Unraveling this alternative mode of action of cryoprotection should help in the directed design of novel cryoprotective agents, which might be less cytotoxic than classical, empirically-found cryoprotective agents.
机译:快速的冷却和再加热已被证明是对冷冻储存活细胞的承诺,不能通过常规缓慢冷冻方法保存。然而,成功受高度浓缩的冷冻保护剂的细胞毒性的限制。最近的结果表明,冷冻保护剂不需要完全抑制细胞内冰晶以允许在冷冻保存后存活。 DMSO或乙二醇等冷冻保护剂也可以导致细胞展示细胞内冰。然而,不清楚这种耐受机构实现了这种耐受性。还已知这些物质调节细胞膜的性质。这里示出了冷冻保护DMSO和乙二醇对HeLa细胞的质膜中脂质的迁移性有明显影响。为了将血浆膜的性质从对冰形成的影响隔离,在不存在冷冻保护剂的情况下调节膜性质。这是通过改变甾醇含量来实现的。在甾醇含量升高的细胞中,存在固定脂质部分,类似于用DMSO和乙二醇处理的细胞。在没有经典冷冻保护剂的情况下,这些细胞在快速冷冻和解冻后也显着增加了血浆膜完整性。然而,它们的细胞内溶酶体不能富含甾甾体,仍然破裂。这些结果清楚地表明膜特性的调节可以传达冷冻保护。冷却缓慢时,甾醇含量升高实际上对血浆膜具有不利影响,这表明这种效果是特异性的快速,非平衡冷却过程。解开这种冷冻保护的替代作用模式应该有助于新型冷冻保护剂的指导设计,这可能比经典的经验发现的冷冻保护剂更少细胞毒性。

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    Jan Huebinger;

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  • 年度 2018
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  • 原文格式 PDF
  • 正文语种 eng
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