摘要
目的 研究细胞周期蛋白激酶抑制因子p2 1基因转染对人晶状体上皮细胞 (lensepithelialcells ,LEC)周期调控的影响 ,在基因水平探讨防治后发性白内障的可能性。方法 构建含人p2 1基因真核表达的载体质粒pcDNA3/p2 1,采用基因转染技术将质粒DNA转染至永生性人LEC系HLE B3,使用流式细胞仪观察细胞生长和周期的变化 ,并采用逆转录聚合酶链式反应方法检测p2 1mRNA的表达 ;分别采用免疫组化和免疫印迹 (westernblotting,WB)方法检测p2 1蛋白的表达。结果 体外构建的载体质粒pcDNA3/p2 1经酶切鉴定含有人p2 1基因全长cDNA片段。基因转染后细胞HLE B3经传代培养 ,4 8h后出现缓慢生长且部分细胞漂浮死亡的现象 ,G1期细胞明显增多。与对照细胞比较 ,转染后细胞的p2 1mRNA表达明显增多 ;p2 1蛋白表达明显增强 ,在经筛选的阳性克隆细胞中WB方法可检测到相对分子质量为 2 10 0 0的阳性蛋白带。结论 外源性p2 1基因可在人LEC系HLE B3中过度表达 ,并对细胞周期调控产生抑制作用。基因转染抑制LEC增殖可能成为防治后发性白内障的新途径。
Objective To investigate the effects of transfected exogenous p21 gene on the cells cycle of HLE B3 cells line. The feasibility of prevention of secondary cataract by gene therapy was evaluated. Methods Total length of human p21 gene cDNA was cloned on the parent′s plasmid pcDNA3 to construct the recombinant plasmids of pcDNA3/p21, a large amount of pcDNA3/p21 plasmid DNA was prepared by QIAGEN endofree maxi kit. After harvest of the plasmid DNA, the HLE B3 cells line was transfected. The cell growth was observed and the cells cycle was analyzed by flow cytometry. The expression of p21 mRNA was detected by RT PCR and the expression of p21 protein was detected by immunohistochemistry and western blot analysis. Results Forty eight hours after transfection, the growth of transfected cells became slower, some cells floated and died; the control cells and blank plasmid (blank pcDNA3) transfected cells grew normally. Flow cytometry analysis revealed that the number of cells in G 1 phase increased markedly in transfected cells. The RT PCR showed that the product of p21 in the transfected cells (dead or alive cells) was obviously higher than that of the controls. Immunohistochemical studies showed few positive cells in the controls, and very high positive signal was detected after transfection. Western blot showed a positive band at the level of 21 000 in transfected cells, no positive band could be found in the controls. Conclusion Exogenous p21 gene can transfect the HLE B3 cells and can be expressed. The transfection can affect the cells cycle by G 1 arrest and induces cells death through the apoptosis process. This result suggests that it is possible to prevent the occurrence of secondary cataract by gene therapy.
出处
《中华眼科杂志》
CAS
CSCD
北大核心
2003年第4期209-214,共6页
Chinese Journal of Ophthalmology
基金
国家自然科学基金资助项目 ( 3 9870 80 3
3 9970 781)
中山大学"2 11"重点学科基金资助项目 ( 980 12 )