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非热常压等离子体是一种极好的工具,可以激活各种中胚层来源的人类成体干细胞的增殖。

Non-thermal atmospheric pressure plasma is an excellent tool to activate proliferation in various mesoderm-derived human adult stem cells.

机构信息

Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.

Department of Electrical Engineering, Pusan National University, Pusan, 46241, Republic of Korea.

出版信息

Free Radic Biol Med. 2019 Apr;134:374-384. doi: 10.1016/j.freeradbiomed.2019.01.032. Epub 2019 Jan 24.

Abstract

Adult stem cells are capable of self-renewal and differentiation into specific cell types in tissues and have high potential for stem cell therapy. Mesenchymal and hematopoietic stem cells are easily attainable from the human body and have become applicable tools for adult stem cell therapy. However, there are still technical barriers for the application of mesenchymal and hematopoietic stem cells for therapy, such as the small number of cell populations, high risk of contamination, and loss of their stemness properties in vitro. In our previous study, we showed that non-thermal atmospheric pressure plasma (NTAPP) promoted the proliferation of adipose tissue-derived stem cells (ASCs) by 1.6-fold on average, while maintaining their stemness. Here, we examined the feasibility of NTAPP as a tool to activate the proliferation of mesenchymal and hematopoietic stem cells in vitro without affecting their stem cell characteristics. NTAPP increased the proliferation of bone marrow-derived stem cells (BM-MSCs) and hematopoietic stem cells (HSCs) by 1.8- and 2-fold, respectively, when compared to that of untreated cells. As observed in ASCs, NTAPP exposure also activated the expression of stem cell-specific surface markers, CD44 and CD105, by 5-fold in BM-MSCs, when compared to that in unexposed control cells in a low glucose medium with a low concentration of basic fibroblast growth factor (b-FGF). In addition, NTAPP exposure highly augmented the mRNA expression of well-known pluripotent genes for stemness, such as Oct4, Sox2, and Nanog in ASCs and BM-MSCs when compared to that in unexposed control cells. When cell cycle progression was examined, the G1-S shift was accelerated, and expression of PCNA was increased in NTAPP-exposed ASCs when compared to that in untreated control cells, suggesting that NTAPP activated G1-S transition. Taken together, these results demonstrated that NTAPP activated the proliferation of various mesodermal-derived human adult stem cells by accelerating the G1-S transition while maintaining their pluripotency and stemness, strongly suggesting that NTAPP can be an efficient tool for expanding the population of various adult stem cells in vitro for medical applications.

摘要

成体干细胞具有自我更新和分化为组织中特定细胞类型的能力,具有很高的干细胞治疗潜力。间充质干细胞和造血干细胞容易从人体中获得,已成为成体干细胞治疗的应用工具。然而,间充质干细胞和造血干细胞在治疗中的应用仍然存在技术障碍,例如细胞群体数量少、污染风险高以及体外失去干细胞特性等。在我们之前的研究中,我们表明非热常压等离子体(NTAPP)可使脂肪组织来源的干细胞(ASCs)的增殖平均增加 1.6 倍,同时保持其干细胞特性。在这里,我们研究了 NTAPP 作为一种在不影响其干细胞特性的情况下体外激活间充质和造血干细胞增殖的工具的可行性。与未处理的细胞相比,NTAPP 分别使骨髓来源的干细胞(BM-MSCs)和造血干细胞(HSCs)的增殖增加了 1.8 倍和 2 倍。与未暴露于 NTAPP 的对照细胞相比,在低糖培养基中添加低浓度碱性成纤维细胞生长因子(b-FGF)时,暴露于 NTAPP 还使 BM-MSCs 中的干细胞特异性表面标志物 CD44 和 CD105 的表达增加了 5 倍。此外,与未暴露于 NTAPP 的对照细胞相比,NTAPP 暴露还高度增加了 ASCs 和 BM-MSCs 中与干细胞特性相关的已知多能基因(如 Oct4、Sox2 和 Nanog)的 mRNA 表达。当检查细胞周期进展时,与未处理的对照细胞相比,G1-S 转变加速,并且 NTAPP 暴露的 ASCs 中的 PCNA 表达增加,这表明 NTAPP 激活了 G1-S 转变。总之,这些结果表明,NTAPP 通过加速 G1-S 转变激活了各种中胚层来源的人类成体干细胞的增殖,同时保持了它们的多能性和干细胞特性,强烈表明 NTAPP 可作为体外扩增各种成体干细胞群体的有效工具,用于医学应用。

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