热诱导海藻糖导入原代大鼠肝细胞

Xiaoming He, Arthi A. Amin, A. Fowler, M. Toner
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引用次数: 22

摘要

海藻糖通过热诱导细胞膜改变的途径被引入悬浮大鼠原代肝细胞。将肝细胞悬浮在含有0.4 M海藻糖的稀释肝细胞培养液(培养基:dH2O = 1:2)中进行热处理。在添加海藻糖的培养基中,将肝细胞加热到39°C 10分钟后,使用高效液相色谱(HPLC)检测到大量的细胞质海藻糖(0.07 M)。保留了较高的细胞活力(约90%)。加热1-2小时后,细胞质海藻糖浓度达到平稳(约0.16 M),但加热30分钟后,细胞活力显著下降(<约72%)。进一步发现,通过每10分钟在0°C至39°C之间重复加热1 h(0 - 39°C, 1 h),可以保持较高的细胞活力(约83%),并获得较高的细胞质海藻糖浓度(约0.13 M)。trehalose-lade……
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thermally Induced Introduction of Trehalose into Primary Rat Hepatocytes
Trehalose was introduced into suspended primary rat hepatocytes through pathways resulting from thermally induced alterations of the cellular membrane. The hepatocytes were suspended in a diluted hepatocyte culture medium (medium:dH2O = 1:2) with 0.4 M trehalose during thermal treatments. A significant amount of cytoplasmic trehalose (0.07 M) was detected using high-performance liquid chromatography (HPLC) after heating hepatocytes to 39°C for 10 min in trehalose-supplemented medium. High cell viability (approximately 90%) was retained. The cytoplasmic trehalose concentration reached a plateau (approximately 0.16 M) after heating for 1–2 h. However, the cell viability decreased significantly after 30 min of heating (< approximately 72%). It was further found that by repetitive heating between 0°C and 39°C every 10 min for 1 h (0–39°C, 1 h), high cell viability (approximately 83%) could be maintained and a high cytoplasmic trehalose concentration (approximately 0.13 M) could be obtained. The trehalose-lade...
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