腺病毒介导的p27基因表达对HL-60和Raji细胞株增殖和凋亡的影响

Qinhong Wang, Min Zhang, Huahua Fang, Xiaoxuan Nie, Li Gao, Yan Liu, Yanghui Xie, Yi Xie
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引用次数: 5

摘要

目的:探讨p27基因表达对HL-60和Raji细胞株增殖和凋亡的影响。方法:采用腺病毒介导p27基因转染的方法转染HL-60和Raji细胞。采用X-gal染色、RT-PCR和流式细胞术检测Adp27感染的效果及p27 mRNA和蛋白的表达。采用台盼蓝染色法、MTT法、Annexin V/PI法和DNA阶梯电泳法观察HL-60和Raji细胞的增殖和凋亡情况。结果:HL-60和Raji细胞的感染率分别为40.3%和32%;RT-PCR和流式细胞术显示,Adp27感染的HL-60和Raji细胞p27 mRNA和蛋白均有显著表达,而HL-60细胞本身p27 mRNA和蛋白表达微弱,Raji细胞几乎不表达p27 mRNA和蛋白。细胞生长曲线和MTT实验表明,Adp27对HL-60和Raji细胞具有较强的增殖抑制作用,且具有时间依赖性。Adp27感染HL-60和Raji细胞72 h后,Annexin V+/PI-凋亡细胞率分别为46.9%和35.7%,较对照组(分别为4.7和5.6%)显著升高。在Adp27感染48 h后,HL-60和Raji细胞中检测到典型的DNA阶梯带。结论:腺病毒载体介导的p27基因感染HL-60和Raji细胞可明显抑制细胞增殖,促进细胞凋亡,为利用腺病毒介导的p27基因途径治疗白血病/淋巴瘤提供实验依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of adenovirus-mediated p27 gene expression on the proliferation and apoptosis of HL-60 and Raji cell lines.

Objective: To explore the possible effect of p27 gene expression on the proliferation and apoptosis of HL-60 and Raji cell lines.

Methods: The infections of HL-60 and Raji cells were performed by the adenovirus-mediated p27 gene transfection approach. The efficiency of Adp27 infection and the expression of p27 mRNA and protein were evaluated by X-gal staining, RT-PCR and flow cytometry. The proliferation and apoptosis of HL-60 and Raji cells were estimated by using trypan blue staining, MTT assay, Annexin V/PI and DNA ladder electrophoresis.

Results: The infection efficiency of HL-60 and Raji cells were 40.3 and 32%, respectively; RT-PCR and flow cytometry showed that there were significant expressions of p27 mRNA and protein of HL-60 and Raji cells infected by Adp27, while HL-60 cells themselves showed only faint p27 mRNA and protein, and Raji cells hardly presented p27 mRNA and protein. The strong proliferation inhibitions, which were in a time-dependent manner for HL-60 and Raji cells infected by Adp27, were indicated by cell growth curve and MTT assay. After 72 h infection of HL-60 and Raji cells by Adp27, the Annexin V+/PI- apoptotic cell rates were 46.9 and 35.7% respectively, which were significantly increased compared with control group (4.7 and 5.6% respectively). The typical DNA ladder bands were detectable in HL-60 and Raji cells after 48 h of Adp27 infection.

Conclusion: The infection of HL-60 and Raji cells by means of adenoviral vector-mediated p27 gene could evidently inhibit cellular proliferation and promote cell apoptosis, which would provide experimental evidence for gene therapy of leukemia/lymphoma using adenovirus-mediated p27 gene approach.

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