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用抗坏血酸处理的中枢神经系统前体细胞神经元分化过程中基因表达谱的变化。

Changes of gene expression profiles during neuronal differentiation of central nervous system precursors treated with ascorbic acid.

作者信息

Yu Dong-Hyun, Lee Ki-Hwan, Lee Ji-Yeon, Kim Sujong, Shin Dong-Mi, Kim Jin-Hyuk, Lee Young-Seek, Lee Yeon-Sook, Oh Sun Kyung, Moon Shin Yong, Lee Sang-Hun, Lee Yong-Sung

机构信息

Department of Biochemistry, College of Medicine, Hanyang University, Seoul, Republic of Korea.

出版信息

J Neurosci Res. 2004 Oct 1;78(1):29-37. doi: 10.1002/jnr.20220.

Abstract

Ascorbic acid (AA) has been shown to increase the yield of dopaminergic (DA) neurons derived from basic fibroblast growth factor (bFGF)-expanded mesencephalic precursors. To understand the molecular mechanisms underlying this phenomenon, we used cDNA microarray analysis to examine differential expression of neuronal genes following AA treatment. The putative precursor cells were isolated from E13 rat ventral mesencephalons and expanded in the presence of bFGF. Cells were incubated in mitogen-free media supplemented with 200 microM AA or were left untreated as a control, and total RNA was isolated at different time points (expansion stage and 1, 3, and 6 days after induction of differentiation) and subjected to cDNA microarray analysis. Differentiation was evaluated by Western blot analysis and immunocytochemistry of neuron-specific markers. AA treatment of the mesencephalic precursors increased the expression of neuronal (MAP2) and astrocytic (glial fibrillary acidic protein) markers and the percentage of tyrosine hydroxylase (TH)-positive cells. The microarray analysis revealed that 12 known genes were up-regulated and 20 known genes were down-regulated in expansion-stage AA-treated cells. Six days after the induction of differentiation, AA-treated cells showed up-regulation of 48 known genes and down-regulation of 5 known genes. Our results identified several proteins, such as transferrin, S-100, and somatostatin, as being differentially regulated in AA-treated mesencephalic precursors. This novel result may lead to a better understanding of the molecular mechanisms underlying the AA-induced differentiation of mesencephalic precursors into DA neurons and may form the basis for improved DA neuronal production for treatment of Parkinson's disease patients.

摘要

已证明抗坏血酸(AA)可提高源自碱性成纤维细胞生长因子(bFGF)扩增的中脑前体细胞的多巴胺能(DA)神经元产量。为了解这一现象背后的分子机制,我们使用cDNA微阵列分析来检测AA处理后神经元基因的差异表达。从E13大鼠腹侧中脑中分离出假定的前体细胞,并在bFGF存在的情况下进行扩增。将细胞在补充有200 microM AA的无丝裂原培养基中孵育,或作为对照不进行处理,在不同时间点(扩增阶段以及诱导分化后的1、3和6天)分离总RNA,并进行cDNA微阵列分析。通过蛋白质印迹分析和神经元特异性标志物的免疫细胞化学来评估分化情况。用AA处理中脑前体细胞可增加神经元标志物(微管相关蛋白2)和星形胶质细胞标志物(胶质纤维酸性蛋白)的表达以及酪氨酸羟化酶(TH)阳性细胞的百分比。微阵列分析显示,在扩增阶段经AA处理的细胞中,有12个已知基因上调,20个已知基因下调。诱导分化6天后,经AA处理的细胞显示48个已知基因上调,5个已知基因下调。我们的结果确定了几种蛋白质,如转铁蛋白、S-100和生长抑素,在经AA处理的中脑前体细胞中受到差异调节。这一新颖的结果可能有助于更好地理解AA诱导中脑前体细胞分化为DA神经元背后的分子机制,并可能为改善用于治疗帕金森病患者的DA神经元生成奠定基础。

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