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诱导热休克蛋白可增强冻融脂肪组织来源干细胞的干性。

Inducing Heat Shock Proteins Enhances the Stemness of Frozen-Thawed Adipose Tissue-Derived Stem Cells.

作者信息

Shaik Shahensha, Hayes Daniel, Gimble Jeffrey, Devireddy Ram

机构信息

1 Bioengineering Laboratory, Department of Mechanical Engineering, Louisiana State University , Baton Rouge, Louisiana.

2 Department of Biomedical Engineering, Pennsylvania State University , University Park, Pennsylvania.

出版信息

Stem Cells Dev. 2017 Apr 15;26(8):608-616. doi: 10.1089/scd.2016.0289. Epub 2017 Feb 16.

Abstract

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.

摘要

已经进行了广泛的研究,以确定冷冻方案和冷冻保存剂对脂肪组织来源的基质/干细胞(ASC)以及其他细胞活力的影响。不幸的是,经过数十年使用基本相似的冷冻保存技术的研究,人们可能得出的结论是存在一个障碍,这阻碍了完全恢复。我们假设,能够诱导一部分热休克蛋白(HSP)和伴侣蛋白的试剂将减少ASC解冻后恢复的内在障碍。将ASC暴露于43°C 1小时以上调HSP,通过进行定量聚合酶链反应(PCR)和蛋白质印迹分析来确定热休克后HSP的时间表达谱。发现热休克后3小时HSP70和HSP32的表达水平最高,而HSP90和HSP27保持不变。在最大HSP表达期间冷冻保存的热休克ASC解冻后的活力比未热休克的样品有所增加。组织化学染色和定量逆转录PCR表明ASC的分化潜能得以保留。因此,表明在冷冻损伤前上调HSP对ASC有益,并且是使用有害冷冻保护剂的潜在替代方法。

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