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腺相关病毒介导的狨猴 P53基因沉默

石亮 张晨 向志光 邓仪晨 苏静芬 刘云波

中国比较医学杂志2016,Vol.26Issue(4):53-57,5.
中国比较医学杂志2016,Vol.26Issue(4):53-57,5.DOI:10.3969/j.issn.1671-7856.2016.04.009

腺相关病毒介导的狨猴 P53基因沉默

Adeno-associated virus mediated p53 gene silence in marmosets

石亮 1张晨 2向志光 1邓仪晨 1苏静芬 1刘云波1

作者信息

  • 1. 中国医学科学院医学实验动物研究所,北京 100021
  • 2. 北京大学生命科学学院,北京 100871
  • 折叠

摘要

Abstract

Objective To decrease the p53 gene expression at cellular and animal levels in marmoset using RNA interference technique.Methods The shRNA interference sequences were designed and inserted into the adeno-associated virus vector plasmid after bioinformatics analysis.The plasmids were transfected into African green monkey kidney cos-7 cells.The suppression of p53 mRNA was detected by real-time PCR, and the changes of p53 protein expression were detected by Western bolt.The adeno-associated virus-8 was injected through the hind leg vein.The changes of p53 protein expression in the liver tissue was detected by Western blot and immunohistochemistry.Results We screened two RNA interference effective arget sequences.The expression of p53 mRNA was suppressed ( 82.7 ±8.1 )% and ( 80.7 ± 7.5)%, respectively (P<0.05), and the expression of p53 protein was decreased (77.3 ±11.5)% and (73.7 ± 10.7)%, respectively (P<0.05).The two marmosets after virus infection showed that there were virus distributions in the liver, testes, and neck detected by in vivo fluorescence imaging.The expression of p53 in the marmoset liver was detected by western blot, immunohistochemistry analysis showing no obvious changes.Conclusions In the present study, the decrease of P53 gene expression at cellular level is achieved, however, the liver P53 protein in the marmoset liver is not significantly changes.Further optimization of the way of infection is needed in the future.

关键词

AAV8/P53/RNA干扰/狨猴

Key words

AAV8 virus/p53/RNA interference/Marmoset

分类

医药卫生

引用本文复制引用

石亮,张晨,向志光,邓仪晨,苏静芬,刘云波..腺相关病毒介导的狨猴 P53基因沉默[J].中国比较医学杂志,2016,26(4):53-57,5.

基金项目

国家科技支撑计划(No.2014BAI03B01)。 ()

中国比较医学杂志

OA北大核心CSTPCD

1671-7856

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