Xiangyue Hu, Haoyun Duan, Dulei Zou, Chunxiao Dong, Yani Wang, Yao Wang, Zongren Li, Zongyi Li
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Finally, changes in gene expression levels were examined using quantitative polymerase chain reaction (qPCR) in the presence of appropriate primers.</p><p><strong>Results: </strong>Compared with normal cells in the control group, the morphology of experimental cells subjected to acoustic vibration did not significantly change. Contrastingly, the colony-forming efficiency of the experimental cells significantly increased. Immunofluorescence staining results showed the cells in experimental group were positive for the pluripotency markers NANOG, octamer-binding transcription factor 4 gene (OCT4), and SRY (sex determining region Y)-box 2 (SOX2). 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引用次数: 0
摘要
研究目的本研究旨在探讨声学振动对人类胚胎干细胞(hESCs)多能性的影响,并评估处理后细胞的增殖和自我更新能力:实验使用人类 ES 细胞株 H1。方法:实验采用人 ES 细胞系 H1,用声波振动装置处理 hESC,然后用集落形成试验检测其增殖能力,并通过免疫荧光染色检测多能性相关标记物的表达。最后,在适当引物的作用下,使用定量聚合酶链反应(qPCR)检测基因表达水平的变化:结果:与对照组的正常细胞相比,声学振动实验组细胞的形态没有明显变化。相反,实验组细胞的集落形成效率明显提高。免疫荧光染色结果显示,实验组细胞的多能性标志物NANOG、八聚体结合转录因子4基因(OCT4)和SRY(性别决定区Y)-box 2(SOX2)呈阳性。此外,多能性基因NANOG、OCT4、SOX2和Yes相关蛋白(YAP)相关基因的表达水平在声学振动后上调:我们的研究结果表明,声学振动增强了 hESCs 的增殖能力,提高了 NANOG、OCT4、SOX2 和 YAP 相关基因的表达水平,表明声学振动可以优化 hESCs 的自我更新能力,YAP 信号通路可能在声学振动的功能过程中发挥了关键作用。
Acoustic vibration promotes in vitro expansion of human embryonic stem cells.
Objectives: This study aimed to investigate the effect of acoustic vibration on the pluripotency of human embryonic stem cells (hESCs) and evaluate cell proliferation and self-renewal ability post-treatment.
Methods: The human ES cell line H1 was used for the experiments. hESCs were treated with an acoustic vibration device. Their proliferative ability was subsequently detected using a colony formation assay, while the expression of pluripotency-related markers was detected via immunofluorescence staining. Finally, changes in gene expression levels were examined using quantitative polymerase chain reaction (qPCR) in the presence of appropriate primers.
Results: Compared with normal cells in the control group, the morphology of experimental cells subjected to acoustic vibration did not significantly change. Contrastingly, the colony-forming efficiency of the experimental cells significantly increased. Immunofluorescence staining results showed the cells in experimental group were positive for the pluripotency markers NANOG, octamer-binding transcription factor 4 gene (OCT4), and SRY (sex determining region Y)-box 2 (SOX2). In addition, the expression levels of pluripotency genes NANOG, OCT4, SOX2, and Yes-associated protein (YAP)-related genes were up-regulated following acoustic vibration.
Conclusions: Our results revealed that acoustic vibration enhanced the proliferative ability of hESCs and increased the expression levels of NANOG, OCT4, SOX2, and YAP-related genes, indicating that acoustic vibration can optimize the self-renewal ability of hESCs and that the YAP signaling pathway may play a critical role in the functional process of acoustic vibration.