诱导热休克蛋白可增强冻融脂肪组织来源干细胞的干性

Stem cells and development Pub Date : 2017-04-15 Epub Date: 2017-02-16 DOI:10.1089/scd.2016.0289
Shahensha Shaik, Daniel Hayes, Jeffrey Gimble, Ram Devireddy
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引用次数: 0

摘要

为了确定冷冻方案和冷冻剂对脂肪组织衍生基质/干细胞(ASCs)以及其他细胞活力的影响,人们进行了大量的研究。遗憾的是,经过数十年利用基本相似的冷冻保存技术进行的研究,人们得出的结论是存在一个障碍,阻碍了细胞的完全恢复。我们假设,能够诱导热休克蛋白(HSPs)和伴侣蛋白子集的药剂将减少ASCs解冻后恢复的内在障碍。将 ASCs 暴露于 43°C 1 小时以上调 HSPs,并通过定量聚合酶链反应(PCR)和 Western 印迹检测确定热休克后 HSP 的时间表达谱。结果发现,热休克后3小时,HSP70和HSP32的表达水平最高,而HSP90和HSP27则保持不变。与未受热休克的样本相比,在 HSPs 表达达到最高水平时冷冻保存的受热休克 ASCs 在解冻后的存活率有所提高。组织化学染色和定量反转录-PCR表明,ASC的分化潜能得以保留。因此,在冷冻之前上调 HSPs 对 ASCs 是有益的,是使用有害冷冻保护剂的一种潜在替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inducing Heat Shock Proteins Enhances the Stemness of Frozen-Thawed Adipose Tissue-Derived Stem Cells.

Extensive research has been performed to determine the effect of freezing protocol and cryopreservation agents on the viability of adipose tissue-derived stromal/stem cells (ASCs) as well as other cells. Unfortunately, the conclusion one may draw after decades of research utilizing fundamentally similar cryopreservation techniques is that a barrier exists, which precludes full recovery. We hypothesize that agents capable of inducing a subset of heat shock proteins (HSPs) and chaperones will reduce the intrinsic barriers to the post-thaw recovery of ASCs. ASCs were exposed to 43°C for 1 h to upregulate HSPs, and the temporal HSP expression profile postheat shock was determined by performing quantitative polymerase chain reaction (PCR) and western blotting assays. The expression levels of HSP70 and HSP32 were found to be maximum at 3 h after the heat shock, whereas HSP90 and HSP27 remain unchanged. The heat shocked ASCs cryopreserved during maximal HSPs expression exhibited increased post-thaw viability than the nonheat shocked samples. Histochemical staining and quantitative reverse transcription-PCR indicated that the ASC differentiation potential was retained. Thus, suggesting that the upregulation of HSPs before a freezing insult is beneficial to ASCs and a potential alternative to the use of harmful cryoprotective agents.

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