Maryam Sadeghi-Zadeh, Farshad Homayouni Moghadam, Mohammad Hossein Nasr-Esfahani
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Mouse neural stem cells (mNSCs) were treated with FA and expressions of TH</b> <b>(tyrosine hydroxylase)</b> <b>and NURR1 as the DA neuron specific markers were determined using real time qRT-PCR and immunostaining assays</b> <b><i>.</i> </b> <b>Finally, efficacy of FA on DA differentiation was evaluated in comparison with other methods using fibroblast growth factor 8b (FGF8b) and sonic hedgehog (SHH). Treatment with FA could increase the</b> <b><i>Th</i></b> <b>and</b> <b><i>Nurr1</i></b> <b>gene expressions in mNSCs. Also, it enhanced</b> <b><i>β</i></b> <b>-</b> <b><i>tubullin</i></b> <b>-</b> <b><i>III</i></b> <b>expression and increased the neurite length in treated groups. Real time qRT-PCR and immunostaining assays showed that FA could increase DA differentiation in mNSCs effectively. Also, gene expression profile in some groups showed that FA can raise the differentiation rate of other neuronal subtypes such as cholinergic neurons. 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引用次数: 1
摘要
黑质多巴胺能(DA)神经元的退化被认为是帕金森病(PD)的主要原因。在细胞替代疗法的同时防止DA神经元的丢失,为帕金森病的治疗带来了巨大的希望。为此,人们进行了各种研究,以寻找特异性的DA神经保护化合物或发展DA分化方法。阿魏酸(FA)具有较强的神经保护作用,但其对DA神经元的保护和分化作用尚不明确。用FA处理小鼠神经干细胞(mNSCs),采用实时荧光定量pcr和免疫染色法检测TH(酪氨酸羟化酶)和NURR1作为DA神经元特异性标志物的表达。最后,与其他使用成纤维细胞生长因子8b (FGF8b)和sonic hedgehog (SHH)的方法相比,评估FA对DA分化的效果。FA处理可增加骨髓间充质干细胞Th和Nurr1基因的表达。治疗组β -微管蛋白- III表达增强,神经突长度增加。Real - time qRT-PCR和免疫染色结果显示,FA能有效促进骨髓间充质干细胞的DA分化。此外,在某些组的基因表达谱显示,FA可以提高其他神经元亚型如胆碱能神经元的分化率。FA通过增加NURR1转录因子的表达,有效诱导神经前体细胞DA分化,NURR1转录因子是已知的中脑DA神经元分化的转录因子。
Ferulic Acid Induces NURR1 Expression and Promotes Dopaminergic Differentiation in Neural Precursor Cells.
Degeneration of dopaminergic (DA) neurons in the substantia nigra is known as the main cause of Parkinson's disease (PD). Preventing the loss of DA neurons alongside the cell-replacement therapy have brought tremendous hope for the treatment of PD. For this purpose, various studies have been done to findthe specificDA neuro-protective compounds or progressing DA-differentiation methods. Ferulic acid (FA) has strong neuro-protective effects, but at this point its role on protection and differentiation of DA neurons is not well-defined. Mouse neural stem cells (mNSCs) were treated with FA and expressions of TH(tyrosine hydroxylase)and NURR1 as the DA neuron specific markers were determined using real time qRT-PCR and immunostaining assays.Finally, efficacy of FA on DA differentiation was evaluated in comparison with other methods using fibroblast growth factor 8b (FGF8b) and sonic hedgehog (SHH). Treatment with FA could increase theThandNurr1gene expressions in mNSCs. Also, it enhancedβ-tubullin-IIIexpression and increased the neurite length in treated groups. Real time qRT-PCR and immunostaining assays showed that FA could increase DA differentiation in mNSCs effectively. Also, gene expression profile in some groups showed that FA can raise the differentiation rate of other neuronal subtypes such as cholinergic neurons. FA effectivelyinduces the DA differentiation in neural precursor cells by its ability to increase the expression of the NURR1 transcription factor, which is a known transcription factor for differentiation of midbrain DA neurons.
期刊介绍:
The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).