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人21.5kDaMBP基因沉默对神经胶质瘤细胞增殖与凋亡的作用研究

田瑞敏 王含彦 易芳 王晓明 陈建业

重庆医学Issue(1):10-13,4.
重庆医学Issue(1):10-13,4.DOI:10.3969/j.issn.1671-8348.2015.01.004

人21.5kDaMBP基因沉默对神经胶质瘤细胞增殖与凋亡的作用研究

Effects of the human 21 .5 kDa MBP gene silencing on the proliferation and apoptosis of glioma cells

田瑞敏 1王含彦 2易芳 2王晓明 3陈建业2

作者信息

  • 1. 川北医学院药学院药理学教研室,四川南充637000
  • 2. 川北医学院基础医学院生物化学教研室,四川南充637000
  • 3. 川北医学院附属医院神经内科,四川南充637000
  • 折叠

摘要

Abstract

Objective To investigate the effects of silencing of the human cerebral 21 .5 kDa myelin basic protein (MBP) gene on the proliferation and apoptosis of the glioma U251 cells .Methods The 21 .5 kDa MBP sequence‐specific short hair‐pin RNA (shR‐NA) recombinant plasmids pGenesil‐1‐MBP‐3 were transfected into the human glioma cell line(U251) ,the cells of U251 was used as MBP silencing group ,the cells transfected with negative control plasmids used as negative control group ,and the cells transfected with liposomes used as blank control group .Real‐time PCR and Westernblot were used to detect the expression levels of the 21 .5 kDa MBP mRNA and protein in each group ,and the cell proliferation curve was measured by CCK‐8 assay ,the apoptosis rate was a‐nalysised by Flow cytometry .Results Both the mRNA and the protein expression levels of the 21 .5 kDa MBP of MBP silencing group were significantly lower than those in the control groups (P<0 .05);the cellular proliferation activity of the MBP silencing group decreased significantly (P<0 .05)while the cellular apoptotic rate increased significantly (P<0 .05) .Conclusion Silencing of the human cerebral 21 .5 kDa MBP gene may playa dual role in the inhibition of proliferation and the promotion of apoptosis of the glioma U251 cells .

关键词

RNA干扰/基因沉默/转染/21.5kDaMBP/神经胶质瘤/增殖/凋亡

Key words

RNA interference/genes silencing/transfection/21 .5 kDa MBP/glioma/proliferation/apoptosis

分类

医药卫生

引用本文复制引用

田瑞敏,王含彦,易芳,王晓明,陈建业..人21.5kDaMBP基因沉默对神经胶质瘤细胞增殖与凋亡的作用研究[J].重庆医学,2015,(1):10-13,4.

基金项目

四川省教育厅重点课题基金资助项目(2006J13031);川北医学院2013年青年项目资助(CBY13-A-QN33)。 ()

重庆医学

OA北大核心CSTPCD

1671-8348

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