摘要
目的研究miRNA-132对白血病细胞株K562增殖、凋亡的影响,探讨其可能的作用机制。方法应用Lipofectami-ne TM 2000转染K562细胞,实时荧光定量PCR检测转染后miRNA-132的表达。CCK-8及流式细胞术检测转染后对K562细胞增殖及凋亡的影响。Western Blot法分别检测SRIT1及P53的表达量变化。结果 miRNA-132在正常细胞中的表达明显低于在K562细胞株中的表达,与空白对照组和阴性对照组相比,转染组miRNA-132的表达量明显升高。转染miRNA-132 mim-ics后,K562细胞增殖能力减弱,凋亡率明显增加。与空白对照组和miRNA-132-NC组相比,miRNA-132高表达后,转染组的SIRT1蛋白表达量明显降低,P53蛋白表达量明显升高。结论高表达的miRNA-132对白血病K562细胞有显著的增殖抑制和凋亡诱导作用,其机制可能与其增强SIRT1、P53的活性有关。
Objective To investigate the effect of miRNA-132 on proliferation and apoptosis of leukemia cell line K562,and explore its possible mechanism.MethodsK562 cells were transfected with LipofectamineTM 2000.The expression of miRNA-132 was detected by real-time quantitative PCR.The effect of transfection on proliferation and apoptosis of K562 cells was detected by CCK-8 and flow cytometry.The protein expression levels of SRIT1 and P53 were detected by Western Blot.ResultsThe expression of miRNA-132 in normal cells was significantly lower than that in K562 cells.Compared with the blank group and the negative control group,the expression of miRNA-132 was significantly increased in the transfected group.K562 cells’proliferated and the apoptosis rate decreased significantly after transfection of miRNA-132 mimics.Compared with the blank control group and miRNA-132-NC group,after the high expression of miRNA-132,the expression of SIRT1 protein in the transfected group was significantly decreased,and the expression of P53 protein was significantly increased.ConclusionHighly expression of miRNA-132 significantly inhibits the proliferation of leukemia K562 cells and induces the apoptosis,which may be related to the enhancement of SIRT1 and P53 activity.
作者
樊云秀
李建厂
孙维梅
陈博
FAN Yunxiu;LI Jianchang;SUN Weimei;CHEN Bo(Department of Pediatrics,Binzhou Medical University Hospital,Binzhou256603,P.R.China)
出处
《滨州医学院学报》
2019年第1期9-12,共4页
Journal of Binzhou Medical University