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作 者:韩忠晶[1] 吴明娟[2] 毕武春[1] 张宏宇[1] 肖海凤[1] 魏惠妍[1] 邹朝霞[1] 高旭[1]
机构地区:[1]哈尔滨医科大学生物化学与分子生物学教研室,哈尔滨市150081 [2]黑龙江省中医研究院,哈尔滨市150036
出 处:《医学分子生物学杂志》2012年第5期338-343,共6页Journal of Medical Molecular Biology
基 金:国家自然科学基金(No.81171997,No.81000933),中国博士后科学基金(No.2012M520035),黑龙江省卫生厅基金(No.2009-211)
摘 要:目的观察血红素加氧酶-1(remeoxygehase-1,HO-1)活性改变对人肺腺癌A549细胞失巢凋亡的影响。方法将野生型HO-1(wtHO-1)和失活突变体mHO-1G143H基因与质粒pcDNA3-1(+)连接,构建野生型和突变型HO-1真核表达载体pcDNA3.1(+)-wtHO-1和pcDNA3.1(+)-mHO—1G143H。利用脂质体介导的方法将构建好的重组载体转染人肺腺癌A549细胞构建稳转细胞系,以空载体转染作为对照组。通过G418筛选建立稳定表达野生型和突变型HO-1的人肺腺癌A549细胞系。利用RT—PCR及Western印迹方法检测各稳转细胞系中HO-1mRNA和蛋白的表达水平。悬浮培养上述稳转细胞系,建立失巢凋亡模型:应用流式细胞术检测细胞凋亡情况。结果与空载体对照组相比,野生型HO-1过表达细胞系中,细胞失巢凋亡率明显下降;突变型HO-1过表达细胞系中,细胞失巢凋亡率增高。结论HO-1过表达可能抑制肺腺癌A549细胞的失巢凋亡能力,这种作用可能与HO-1催化活性相关。Objective To determine the effect of heme oxygenase-1 on anoikis in human lung adenocarcinoma cell lines A549. Methods To construct the eukaryotic expression vectors of wild- type HO-1 and HO-1 G143H mutant, named by pcDNA3.1 ( + )-wtHO-1 and pcDNA3.1 ( + )- mHO-1G143H. A549 cells were transfected with wtHO-1 and mHO-1 using lipofectamine 2000, empty vector transfected as a control group. Stable transfected cells were selected by G418. The ex- pression of HO-1 mRNA and protein were detected by RT-PCR and Western blot. Suspension cul- tures of the stable transfected cell lines to establish the model of anoikis and detect the apoptotic a- bility of A549 by Flow Cytometer. Results Compared to the empty group, overexpression of wtHO-1 decrease the apoptosis of A549 cells after detached culture for 72h. On the contrary, over- expression of mHO-1 increase the rate of anoikis of A549 cells. Conclusion Overexpression HO-1 inhibit anoikis of lung adenocarcinoma A549 cells which may be the result of catalytic activity of HO-1.
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