利用基因组芯片和生物信息学分析天然脑溶素对大鼠间充质干细胞基因表达谱的影响

Ying-Hong Li, Zheng-Zhi Wu, Ming Li, Xiu-qin Jia, Min Yang, Manyin Chen
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引用次数: 1

摘要

目的:分析天然脑lycin (Natural Cerebrolycin, NC)对间充质干细胞(Mesenchymal Stem Sells, MSCs)基因表达谱的影响,探讨NC临床应用于阿尔茨海默病(Alzheimer’s Disease, AD)的可行性及其基因分子药效学机制。方法:采用全骨髓贴壁法和贴壁筛选法分离纯化大鼠骨髓间充质干细胞,采用免疫细胞化学染色技术分析细胞同源性。采用Affymetric全基因组基因芯片分析方法分析NC处理的间充质干细胞的差异表达基因。结果:获得了高纯度(90%以上)的大鼠间充质干细胞。NC处理MSCs后,显示45个差异表达基因,其中21个基因表达上调(FC≥2),24个基因表达显著下调(FC≤-2)。这些基因包括参与tgf - β / Bmp、Hedgehog、Bmp和Wnt信号转导通路的基因,这些信号转导通路与细胞分化发育和/或神经系统功能、学习记忆功能有关,参与Ras和G蛋白偶联受体信号转导通路与细胞生长、增殖和凋亡有关,参与MAPKKK级联的基因。结论:NC抗ad的分子基因药效学机制可能与参与调节神经细胞分化发育、神经系统功能、学习记忆功能以及常见细胞生长、分化、增殖和凋亡等信号转导通路的众多基因表达有关。
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Analysis of Effects of Natural Cerebrolysin on the Gene Expression Profile of Mesenchymal Stem Cells in Rats by Genome Chip and Bioinformatics
Objective: In order to analyze the effects of Natural Cerebrolycin (NC) on the gene expression profile of Mesenchymal Stem Sells (MSCs), the feasibility of NC's clinical use for Alzheimer's Disease(AD)and the mechanism of its gene molecular Pharmacodynamics were studied. Method: The MSCs of rats were isolated and purified by whole bone marrow adherence and adherence screening method, the homology of the cells was analyzed by immunocytochemistry staining technique. The differential expression genes of MSCs treated with NC were analyzed by Affymetric whole genome gene chip analysis method. Result: Rat MSCs of higher purity (more than 90%) was acquired. After MSCs were treated with NC, 45 differential expression genes were displayed, the expressions of 21 genes among them were up-regulated (FC≥2) and the expressions of 24 genes were significantly down-regulated (FC≤-2).These genes included the genes participate in TGFβ / BMPs, Hedgehog, Bmp and Wnt signal transduction pathways that have relations with cell differentiation &development and /or nervous system function, and learning and memorizing functions, the genes of Ras and G protein-coupled receptor signaling pathways that have relations with cell growth and proliferation and apoptosis, and the genes of MAPKKK cascading. Conclusion: NC's anti-AD pharmacodynamic mechanism of molecular genes could have relations with numerous gene expressions of some signal transduction pathways, which participate in regulating nerve cell differentiation and development, nervous system function, functions of learning and memory, and common cell functions of growth, differentiation, proliferation and apoptosis.
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