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Differentiation of rat adipose tissue-derived stem cells into neuron-likecells by valproic acid a histone deacetylase inhibitor

机译:大鼠脂肪组织干细胞向神经元样细胞的分化组蛋白脱乙酰基酶抑制剂丙戊酸

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摘要

Valproic acid (VPA) is a widely used antiepileptic drug, which has recently been reported to modulate the neuronal differentiation of adipose tissue-derived stem cells (ASCs) in humans and dogs. However, controversy exists as to whether VPA really acts as an inducer of neuronal differentiation of ASCs. The present study aimed to elucidate the effect of VPA in neuronal differentiation of rat ASCs. One or three days of pretreatment with VPA (2 mM) followed by neuronal induction enhanced the ratio of immature neuron marker βIII-tubulin-positive cells in a time-dependent manner, where the majority of cells also had a positive signal for neurofilament medium polypeptide (NEFM), a mature neuron marker. RT-PCR analysis revealed increases in the mRNA expression of microtubule-associated protein 2 (MAP2) and NEFM mature neuron markers, even without neuronal induction. Three-days pretreatment of VPA increased acetylation of histone H3 of ASCs as revealed by immunofluorescence staining. Chromatin immunoprecipitation assay also showed that the status of histone acetylation at H3K9 correlated with the gene expression of TUBB3 in ASCs by VPA. These results indicate that VPA significantly promotes the differentiation of rat ASCs into neuron-like cells through acetylation of histone H3, which suggests that VPA may serve as a useful tool for producing transplantable cells for future applications in clinicaltreatments.
机译:丙戊酸(VPA)是一种广泛使用的抗癫痫药,最近有报道称它能调节人和狗中脂肪组织干细胞(ASCs)的神经元分化。但是,关于VPA是否真正起ASCs神经元分化的诱导作用存在争议。本研究旨在阐明VPA在大鼠ASCs神经元分化中的作用。用VPA(2 mM)预处理一到三天,然后进行神经元诱导以时间依赖的方式提高了未成熟神经元标记物βIII-微管蛋白阳性细胞的比例,其中大多数细胞的神经丝培养基多肽也有阳性信号(NEFM),一种成熟的神经元标记。 RT-PCR分析显示,即使没有神经元诱导,微管相关蛋白2(MAP2)和NEFM成熟神经元标志物的mRNA表达也会增加。免疫荧光染色显示,VPA的三天预处理增加了ASC组蛋白H3的乙酰化。染色质免疫沉淀试验还表明,通过VPA,H3K9处组蛋白乙酰化的状态与TUBB3的基因表达相关。这些结果表明,VPA通过组蛋白H3的乙酰化显着促进大鼠ASCs向神经元样细胞的分化,这表明VPA可以作为生产可移植细胞的有用工具,以供将来临床应用治疗。

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