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Effect and Mechanism of Epidermal Growth Factor on Proliferation of GL15 Gliomas Cell Line

机译:表皮生长因子对GL15胶质瘤细胞系增殖的影响及其机制

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The effects of epidermal growth factor (EGF) on proliferation of G15 glioma cells and the possible mechanisms were investigated. GFAP and EGFR expression was detected by immunohistochemical method. After the cells were treated with EGF at different concentrations, cell count method was used to determine the proliferation of glioma cells, cell cycle and apoptosis were analyzed by flow cytometry (FCM), and laser scan confocal microscope (LSCM) was used to measure the cytoplasmic free calcium. The results showed that GFAP was diffusedly expressed in GL15 cells and EGFR was over-expressed. EGF at doses of ≤ 1 ng/mL could significantly stimulate cell proliferation, cells in phase G_0/G_1 decreased, and those in phase S increased. EGF at doses of 10 and 100 ng/ml could inhibit the cell proliferation significantly, and the apoptosis ratio in high dose of EGF group was higher than in control group. EGF could significantly induce a quick rise of intracellular free calcium, but the peak value of intracellular free calcium activated by high dose of EGF was higher than by low dose of EGF. It was suggested that EGF had a dual effect on gliomas: low dose of EGF could stimulate the cell proliferation of gliomas, but high dose of EGF could induce the cell apoptosis and inhibit the proliferation of gliomas, which might be contributed to the difference of intracellular free calcium.
机译:研究了表皮生长因子(EGF)对G15胶质瘤细胞增殖的影响及其可能的机制。免疫组织化学法检测GFAP和EGFR的表达。用不同浓度的EGF处理细胞后,用细胞计数法测定胶质瘤细胞的增殖,用流式细胞仪(FCM)分析细胞周期和凋亡,并用激光扫描共聚焦显微镜(LSCM)测量细胞凋亡。细胞质游离钙。结果表明,GFAP在GL15细胞中弥散表达,而EGFR过表达。 ≤1 ng / mL的EGF可以显着刺激细胞增殖,G_0 / G_1期的细胞减少,而S期的细胞增加。 EGF剂量为10和100 ng / ml可明显抑制细胞增殖,高剂量EGF组细胞凋亡率高于对照组。 EGF可以明显诱导细胞内游离钙的快速升高,但高剂量EGF激活的细胞内游离钙的峰值高于低剂量EGF。提示EGF对神经胶质瘤具有双重作用:低剂量的EGF可刺激神经胶质瘤细胞增殖,而高剂量的EGF可诱导神经胶质瘤细胞凋亡并抑制其增殖,这可能是导致细胞内差异的原因。游离钙。

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