首页  期刊介绍 征稿简则 编委会 期刊征订 广告服务 留言板 English

中国应用生理学杂志 ›› 2018, Vol. 34 ›› Issue (5): 464-469.doi: 10.12047/j.cjap.5661.2018.105

• 研究论文 • 上一篇    下一篇

Beclin-1 shRNA对低氧诱导的SH-SY5Y细胞自噬的影响

卢娜, 李成长, 罗晓秋, 杨坤丽   

  1. 新乡医学院生理学与神经生物学教研室, 河南 新乡 453003
  • 收稿日期:2017-12-26 修回日期:2018-08-06 出版日期:2018-09-28 发布日期:2019-02-21
  • 通讯作者: 卢娜,Tel:13462225817;E-mail:13462225817@163.com E-mail:13462225817@163.com
  • 基金资助:
    河南省教育厅科学技术重点研究项目(14A310009)

Effect of Beclin-1 shRNA on hypoxia-induced autophagy in SH-SY5Y cells

LU Na, LI Cheng-zhang, LUO Xiao-qiu, YANG Kun-li   

  1. Department of Physiology and Neurobiology, Xinxiang Medical University, Xinxiang 453003, China
  • Received:2017-12-26 Revised:2018-08-06 Online:2018-09-28 Published:2019-02-21
  • Supported by:
    河南省教育厅科学技术重点研究项目(14A310009)

摘要: 目的:构建Beclin-1基因短发夹干扰RNA(shRNA)慢病毒载体,感染人SH-SY5Y细胞,观察沉默Beclin-1基因后低氧对SH-SY5Y细胞自噬的影响。方法:构建特异性靶向Beclin-1基因的shRNA慢病毒表达载体和阴性对照序列慢病毒载体;再将载体转染入SH-SY5Y细胞;RT-PCR检测Beclin-1的mRNA表达;Western blot检测Beclin-1蛋白表达;CCK-8法测定Beclin-1 shRNA对SH-SY5Y细胞活力的影响。再将空白对照、阴性对照、转染型三种细胞分别以21%常氧及5%低氧培养,Western blot检测各组细胞LC3蛋白表达;电镜观察自噬小体。结果:Beclin-1 shRNA能明显抑制SH-SY5Y细胞Beclin-1的mRNA及蛋白的表达;沉默Beclin-1基因后,Beclin-1 shRNA组细胞存活率与阴性对照组相比无差异;成功建立了稳定表达Beclin-1 shRNA的SH-SY5Y细胞。5%低氧处理后,与阴性对照组相比较,Beclin-1 shRNA组细胞中LC3Ⅱ/LC3Ⅰ比值下调,细胞内自噬小体数量减少。结论:慢病毒介导的Beclin-1shRNA对SH-SY5Y细胞的活力无影响,但可以抑制低氧诱导的自噬。

关键词: SH-SY5Y, Beclin-1, 自噬, 短发夹RNA

Abstract: Objective: To observe the effect of hypoxia on autophagy in Beclin-1-knockdown SH-SY5Y cells by constructing a stable transfected SH-SY5Y cell lines of silencing Beclin-1 gene. Methods: Beclin-1shRNA lentiviral vector and negative control lentiviral vector were constructed; the vector was transfected into SH-SY5Y cells; then the expression of Beclin-1 mRNA was detected by RT-PCR, the level of Beclin-1 protein was detected by Western blot. CCK-8 method was used to determine the effect of Beclin-1 knockdown on the viability of SH-SY5Y cells. Next, the blank control, negative control and transfected cells were cultured under 21% normoxia and 5% hypoxia conditions. The expression of LC3 protein in each group was detected by Western blot and the autophagic bodies were observed by electron microscopy. Results: Beclin-1 shRNA significantly inhibited the expression of Beclin-1 mRNA and protein in SH-SY5Y cells; after silencing Beclin 1 gene, the survival rate of Beclin-1 shRNA group cells was no different from that of negative control (NC) group. After 5% hypoxia treatment, compared with NC group, the ratio of LC3Ⅱ/LC3Ⅰand the number of autophagy bodies were all decreased in Beclin-1 shRNA group. Conclusion: Beclin-1 knockdown SH-SY5Y cell lines and negative control cell lines were successfully established. Lentivirus-mediated Beclin-1 shRNA has no effect on the viability of SH-SY5Y cells, but can inhibit hypoxia-induced autophagy.

Key words: SH-SY5Y, Beclin-1, autophagy, shRNA

版权所有 © 2015 《中国应用生理学杂志》编辑部
京ICP备16058274号-1
地址:天津市和平区大理道1号,邮编:300050  电话:022-23909086  E-mail:editor@cjap.ac.cn
本系统由北京玛格泰克科技发展有限公司设计开发 技术支持:support@magtech.com.cn