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作 者:朱焱[1,2] 王禄增[1] 杨威[1] 于洋[1] 王维[1] 董婉维[1] 汪瑛[1] 秦英[1] 郑志红[1]
机构地区:[1]中国医科大学实验动物部,沈阳110001 [2]沈阳市公安医院,沈阳110001
出 处:《中国比较医学杂志》2010年第2期17-20,I0002,共5页Chinese Journal of Comparative Medicine
基 金:辽宁省科技计划项目(编号:2006408002-3)
摘 要:目的构建pcDNA3.1-STK15表达质粒,探讨STK15基因对小鼠成纤维细胞(NIH3T3)的影响。方法构建pcDNA3.1-STK15质粒,将其转染NIH3T3,应用RT-PCR、免疫细胞化学和Western印迹方法检测STK15的表达;MTT法检测细胞增殖能力;Transwell检测细胞侵袭能力。结果转染pcDNA3.1-STK15质粒的NIH3T3细胞在48 h有STK15的表达,而且该细胞的增殖速度和穿透Matrigel胶的细胞数均明显高于对照组(P<0.05)。结论STK15基因具有增加细胞增殖和细胞侵袭力的功能,进而形成肿瘤。Objective To investigate the possible effect of STK15 gene on the NIH3T3 fibroblasts.Methods/pcDNA3.1-STK15 expression plasmid was constructed and transient transfected into NIH3T3 cells.The effects of STK15 gene on the NIH3T3 fibroblasts was examined by RT-PCR,immunocytochemistry and Western blot,respectively.The cell proliferation rate was measured by MTT.The capability of cell invasion was observed by Transwell.Results STK15 expression was significantly upregulated in pcDNA3.1-STK15 plasmid-transfected NIH3T3 cells.The MTT showed a significantly increased pcDNA3.1-STK15 plasmid-transfected NIH3T3 cell number invading through Matrigel filter compared with that of pcDNA3.1 vector transfected cells(P0.05).Conclusions/STK15 gene can increase the capability of cell migration and invasion of NIH3T3 fibroblasts in vitro.It may suggest that STK15 gene expression may participate in the process of carcinogenesis.
关 键 词:STK15 细胞转染NIH3T3
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