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作 者:惠玲[1] 邹华[2] 王晓辉[1] 吕同德[1] 哈小琴[1] 李富军[1] 王建峰[1] 杨霄鹏[1] 贾庆华[1]
机构地区:[1]兰州军区总医院医学实验中心,甘肃省干细胞与基因药物研究重点实验室,730050 [2]兰州大学第二附属医院神经内科
出 处:《中华神经外科杂志》2010年第3期267-271,共5页Chinese Journal of Neurosurgery
摘 要:目的观察CIB基因对人胶质瘤SHCcM细胞体外生长和细胞凋亡的影响。方法构建重组质粒pcDNA3-CIB,转染人胶质瘤细胞株SHG44,MTF观察各组细胞的体外生长情况,流式细胞术(FCM)测定各组细胞的细胞周期和凋亡细胞数量,Western—blot检测CIB转染后凋亡相关蛋白的表达变化。结果RT—PCR、Western印迹显示pcDNA3-CIB转染组CIB的mRNA及CIB蛋白表达水平明显高于对照组;与对照组细胞相比,转染CIB的SHG44-CIB组细胞生长明显减缓(P〈0.01),SHG44-CIB组细胞G1、S期细胞减少,G2期细胞增多,凋亡细胞增加至19.2%;凋亡相关蛋白Bcl-2表达下调,Bax表达上调。结论CIB在体外明显抑制SHG44细胞的生长并诱导其发生凋亡,CIB诱导的凋亡可能与Bcl-2及Bax表达的变化相关。Objective To observe the effect of CIB gene on growth and apoptosis of human brain glioma SHG44 cells in vitro. Method Human glioma SHG44 cells were cultured. Recombinant plasmid pcDNA3 - CIB was constructed and transfected into SHG44 cells with Lipofectamine2000. A stable SHG44 cell line with overexpressing of CIB was established for the observation. The cells transfected with blank vector pcDNA3 were used as control effect of CIB on SHG44 cells. The cell growth was observed by MTF method. Flow cytometry (FCM) was used to analyze the cell cycle and apoptotic cells in each group. Then western blotting was used to detect the expression of apoptosis - associated protein. Results The stable transfected cell line SHG44 - CIB was confirmed by RT- PCR and Western blotting. After transfection with CIB, SHG44 cells showed significantly decreased cell proliferation compared with the control groups. The numbers of G1 and S phase cells were decreased, whereas G2 phase cells were increased. The apoptotic rate reached 19. 2% in SHG44 - CIB cells. Overexpression of CIB decreased the expression level of bcl - :2 but increased bax in SHG44 - CIB cells compared with the control groups. Conclusions Overexpression of CIB could inhibit proliferation and induce apoptosis of SHG44. CIB induced apoptosis might work through Bax/Bcl-2 pathway.
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