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Nanosecond pulsed electric fields enhance mesenchymal stem cells differentiation via DNMT1-regulated OCT4/NANOG gene expression

机译:纳秒脉冲电场通过DNMT1调节的OCT4 / NANOG基因表达增强间充质干细胞分化

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摘要

A single nsPEF treatment (5 pulses, less than 10 s) can enhance the differentiation of MSCs. a Schematic of MSCs stimulated by nsPEFs. One million of MSCs were suspended in culture medium in gap cuvette and were subjected to 5 pulses of nsPEFs (i.e., 10 ns at 20 kV/cm and 100 ns at 10 kV/cm). And the time interval between two pulses is 1 s. Then, the trilineage differentiation induction was carried out. b Alizarin Red S, Oil red O staining, and Alcian blue staining for osteogenic, adipogenic, and chondrogenic differentiation at day 14, insets show the no-staining counterparts. c Quantification of differentiation into osteogenic, adipogenic, and chondrogenic lineages. (3 batches of studies were tested with 3 biological donors, values are mean ± SEM from one representative batch with 5 technical repeats, one-way ANOVA, *p ≤ 0.05; **p ≤ 0.01, ***p ≤ 0.001, ****p ≤ 0.0001, NS, p > 0.05) d–f qRT-PCR for the mRNA levels of genes associated with trilineage differentiation (osteogenic: RUNX2, OCN; adipogenic: PPARγ, LPL; chondrogenic: SOX9, COLII) respectively at day 14. (3 batches of studies were tested with 3 biological donors, values are mean ± SEM from one representative batch with 5 technical repeats, one-way ANOVA, *p ≤ 0.05; **p ≤ 0.01, ***p ≤ 0.001, ****p ≤ 0.0001, NS, p > 0.05)
机译:单个NPSPEF处理(5个脉冲,小于10秒)可以增强MSC的分化。由nspefs刺激的MSCs示意图。将一百万MSC悬浮在间隙比色皿中的培养基中,并进行5个NPPEF(即,20kV / cm,10nS,10kV / cm)。两个脉冲之间的时间间隔为1 s。然后,进行Trilineage分化诱导。 B Alizarin Red S,Oil Red O染色和Alcian Blue染色在第14天的骨质,脂肪发生和软骨分化中,插入显示无染色的对应物。 C分化成骨质发生,脂肪发生和软骨形成谱系的定量。 (用3种生物供体测试3批研究,从一个代表批料的值是平均值±SEM,其中5种技术重复,单向ANOVA,*P≤0.05; **P≤0.01,***P≤0.001,* ***p≤0.0001,ns,p> 0.05)D-F qRT-PCR,用于与三叶油分化相关的mRNA水平(osteogensic:runx2,OCN;脂肪生成:PPARγ,LPL;软骨组:SOX9,COLII)分别在第14天。(用3种生物供体测试了3批研究,值是平均值±SEM,从一个代表批次,5种技术重复,单向ANOVA,*P≤0.05; **P≤0.01,***p≤ 0.001,****p≤0.0001,ns,p> 0.05)

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