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作 者:赵丽敏[1] 徐永健[2] 熊盛道[2] 张珍祥[2]
机构地区:[1]河南省人民医院呼吸科,河南郑州450003 [2]华中科技大学同济医学院附属同济医院呼吸科,湖北武汉430030
出 处:《中国病理生理杂志》2007年第1期81-85,共5页Chinese Journal of Pathophysiology
基 金:国家自然科学基金资助项目(No.30270583)
摘 要:目的:转染Kv1.5基因对人气道平滑肌细胞(HASMCs)增殖及凋亡的影响。方法:通过脂质体介导瞬时转染Kv1.5基因于培养的HASMCs中,以转染空载体pRc/CMV的细胞及未转染质粒的细胞为对照;用Westernblotting检测平滑肌细胞Kv1.5蛋白表达;用荧光光度法检测HASMCs胞内钙浓度;用流式细胞术观察细胞周期;用MTT法检测HASMCs增殖及DNA末端转移酶介导的原位缺口末端标记技术(TUNEL)检测细胞的凋亡。结果:(1)转染质粒组Kv1.5蛋白质的表达明显高于未转染组及空载体转染组(P<0.01);(2)转染质粒组细胞胞内钙浓度明显低于未转染组及空载体转染组(P<0.05),且其细胞周期中的G0/G1期细胞比例明显高于、细胞增殖率显著低于未转染组及空载体转染组(P<0.01);同时,转染质粒组细胞的凋亡率明显高于未转染组及空载体转染组(P<0.01)。结论:转染Kv1.5基因能抑制HASMCs的增殖、促进其凋亡,为进一步探讨哮喘气道重塑的机制及其治疗提供实验依据。AIM: To investigate the effect of human Kv1. 5 gene transfection on the proliferation and apoptosis in human airway smooth muscle cells (HASMCs). METHODS: Kv1. 5 gene was transiently transfected into HASMCs with Lipofectamine 2000 and the level of Kv1. 5 protein was observed by Western blotting. Ca2 + concentration in HASMCs was investigated by fluorescent quantitation using fluorospectrophotometer. Flow - cytometry, MTr method and TUNEL were used to detect the effects of Kv1. 5 gene transfection on proliferation and apoptosis in HASMCs. RESULTS : ( 1 ) Western blotting showed that transfection of human Kv1. 5 plasmid significantly increased the Kv1. 5 protein expression compared to control group (P 〈0. 01 ). (2) There was a decrease in Ca^2+ concentration and the numbers of G0/G1 HASMCs in Kv1. 5 gene transfection group compared to control group (P 〈0. 05 ). The proliferation rate in Kv1. 5 gene transfection group was significantly decreased, and the apoptosis rate in Kv1. 5 gene transfection group was significantly increased compared to control group (P 〈0. 01 ). CONCLUSION: Transfection of human Kv1. 5 plasmid inhibits proliferation and increases apoptosis in HASMCs, which provides the experimental evidence for investigating the mechanism and treatment of airway remodeling in asthma.
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