张连昌, 李东韬, 赵学武, 曹新生, 张舒. 流体剪切应力对人骨肉瘤MG-63细胞周期相关基因表达的影响[J]. 解放军医学院学报, 2014, 35(11): 1137-1140. DOI: 10.3969/j.issn.2095-5227.2014.11.016
引用本文: 张连昌, 李东韬, 赵学武, 曹新生, 张舒. 流体剪切应力对人骨肉瘤MG-63细胞周期相关基因表达的影响[J]. 解放军医学院学报, 2014, 35(11): 1137-1140. DOI: 10.3969/j.issn.2095-5227.2014.11.016
ZHANG Lian-chang, LI Dong-tao, ZHAO Xue-wu, CAO Xin-sheng, ZHANG Shu. Effect of flow shear stress on the expression of genes related to cell cycle in human osteosarcoma MG-63 cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2014, 35(11): 1137-1140. DOI: 10.3969/j.issn.2095-5227.2014.11.016
Citation: ZHANG Lian-chang, LI Dong-tao, ZHAO Xue-wu, CAO Xin-sheng, ZHANG Shu. Effect of flow shear stress on the expression of genes related to cell cycle in human osteosarcoma MG-63 cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2014, 35(11): 1137-1140. DOI: 10.3969/j.issn.2095-5227.2014.11.016

流体剪切应力对人骨肉瘤MG-63细胞周期相关基因表达的影响

Effect of flow shear stress on the expression of genes related to cell cycle in human osteosarcoma MG-63 cells

  • 摘要: 目的 观察人骨肉瘤MG-63细胞在流体剪切应力作用后,MG-63细胞中细胞周期相关基因表达谱的变化特点。 方法 MG-63细胞常规培养72 h,随机分成剪切应力作用组和无剪切应力作用对照组。将剪切应力作用组的细胞载玻片置于流体剪切系统中进行实验,流体剪切应力设为1.5 Pa,作用时间为60 min。无剪切应力作用组的细胞静置相同时间。之后分别提取两组的RNA,用Affymetrix公司的全人类基因组芯片进行杂交,并对获得的数据进行分析。 结果 MG-63细胞中细胞周期相关基因表达谱发生改变,247个与细胞周期相关的基因出现差异表达,130个基因表达上调(Fold Change> 2,P< 0.05),117个基因表达下调(Fold Change< -2,P< 0.05)。差异基因主要参与细胞周期多个生物学过程的调控,包括对细胞周期进程、周期阻滞、有丝分裂调控、G1/S转变、有丝分裂间期等生物学过程的调控。 结论 流体剪切应力可以通过改变成骨细胞中细胞周期相关基因的表达,进而调控成骨细胞的增殖和分化等功能。

     

    Abstract: Objective To observe the expression changes of genes related to cell cycle after exposing to fluid shear stress (FSS) in human osteosarcoma MG-63 cells. Methods MG-63 cells were cultured for 72 h, and then they were randomly divided into the fluid shear stress group and the control group. The fluid shear stress group was exposed to 1.5 Pa FSS for 60 min, while the control group was treated with no FSS. Then RNA was extracted from the two groups, and the chip was scanned with Affymetrix gene chip and analyzed for differentially expressed genes. Results The expression of genes related to cell cycle in MG-63 cells was changed. Compared with the control group, 247 genes related to cell cycle showed different expression in the FSS group. Of the 247 genes, 130 genes showed up-regulated (Fold Change> 2, P< 0.05), while the rest of them showed down-regulated (Fold Change< -2, P< 0.05). These differential genes participated in many cell biological progresses, such as cell cycle process, cell cycle arrest, negative regulation of mitotic cell cycle, G1/S transition of mitotic cell cycle, interphase of mitotic cell cycle. Conclusion FSS can stimulate the proliferation and differentiation of MG-63 cells via regulating the expression of genes related to cell cycle.

     

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