短期缺氧对人间充质干细胞增殖、活力和p16(INK4A) mRNA表达的影响:使用脱氧剂的简单缺氧培养系统进行研究

IF 1.1 Q4 CELL & TISSUE ENGINEERING Journal of Stem Cells & Regenerative Medicine Pub Date : 2015-05-30 eCollection Date: 2015-01-01
Akira Ito, Tomoki Aoyama, Makoto Yoshizawa, Momoko Nagai, Junichi Tajino, Shoki Yamaguchi, Hirotaka Iijima, Xiangkai Zhang, Hiroshi Kuroki
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引用次数: 0

摘要

在干细胞中,缺氧环境被认为是维持干细胞的干性和抑制细胞衰老的重要因素。因此,在细胞扩增和/或诱导预期分化过程中,缺氧条件被诱导。然而,这些条件的诱导需要一个专门装备的缺氧室和昂贵的气体混合物,这是昂贵的和空间消耗。由于这些限制,在细胞运输过程中不能提供适当的缺氧条件,而再生医学越来越需要这种条件。因此,需要一种简单而经济的培养系统。本研究的目的是利用CulturePal系统(CulturePal- 0和CulturePal- 5)研究短期缺氧条件对人间充质干细胞(MSC)增殖、活力和衰老的影响,CulturePal系统是一种新型的简单缺氧培养系统,内置脱氧剂。观察到CulturePal-Zero中的O2浓度降至
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The effects of short-term hypoxia on human mesenchymal stem cell proliferation, viability and p16(INK4A) mRNA expression: Investigation using a simple hypoxic culture system with a deoxidizing agent.

A hypoxic environment is thought to be important for the maintenance of stemness and suppressing cell senescence, in stem cells. Therefore, a hypoxic condition is induced during cell expansion and/or induction of intended differentiation. However, the induction of these conditions requires a specially equipped hypoxia chamber and expensive gas mixtures, which are expensive and space-consuming. Owing to these restrictions, appropriate hypoxic conditions cannot be provided during cell transportation, which is increasingly required for regenerative medicine. Hence, a simple and economical culture system is required. The purpose of this study was to investigate the effects of short-term hypoxic conditions on human mesenchymal stem cell (MSC) proliferation, viability, and senescence, utilizing the CulturePal system (CulturePal-Zero and CulturePal-Five), a novel and simple hypoxic culture system with a built-in deoxidizing agent. The O2 concentration in the CulturePal-Zero was observed to reduce to <0.1% within 1 h, and to 5% within 24h in the CulturePal-Five system. Cell proliferation under these hypoxic conditions showed a sharp increase at 5% O2 concentration, and no noticeable cell death was observed even at severe hypoxic conditions (<0.1% O2) up to 72h. The p16(INK4A) (cell senescence marker) mRNA expression was retained under hypoxic conditions up to 72h, but it was up-regulated under normoxic conditions. Interestingly, the p16(INK4A) expression altered proportionately to the O2 concentration. These results indicated that the short-term hypoxic condition, at an approximate O2 concentration of 5%, would be suitable for promoting cell proliferation and repressing cell senescence, without aggravating the MSC viability. Therefore, the CulturePal systems may be suitable for providing an appropriate hypoxic condition in stem cell research and transportation.

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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
5
审稿时长
14 weeks
期刊最新文献
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