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MMP9、S100A10基因沉默稳转小鼠细胞系的构建及验证

陈雪雯 朱红梅 温海

中国真菌学杂志2017,Vol.12Issue(1):19-22,18,5.
中国真菌学杂志2017,Vol.12Issue(1):19-22,18,5.

MMP9、S100A10基因沉默稳转小鼠细胞系的构建及验证

Construction and verification of stable down-regulated MMP9, S100A10 mouse brain microvascular endothelial cell lines

陈雪雯 1朱红梅 1温海1

作者信息

  • 1. 上海市长征医院皮肤科 全军真菌病重点实验室 上海市医学真菌分子生物学重点实验室,上海200003
  • 折叠

摘要

Abstract

Objective To construct stable down-regulated MMP9,S100A10 mouse brain microvascular endothelial cell lines,then verify the reduction level of gene expression.Methods By transfecting LV-musMMP9-shRNA,LV-musS100A10-shRNA into b.End3 respectively,then the very cell lines were screened by puromycin.The obtained differential b.End3 cell lines were observed by fluorescence microscope and varified by RT-qPCR.Results The study successfully constructed stable transfected cell lines which could effectively interference S100A10,MMP-9 expression of 3 × 108 TU/mL and 1 × 108 TU/mL LV-musS100A10-shRNA respectively.Conclusions The targeted down-regulation b.End3 cell lines are useful for further exploring the role of molecule S100A10 or MMP-9 in host blood-brain barrier by control variables and the possible target of treatment exploration of cryptococcal encephalitis/meningitis.

关键词

慢病毒载体/基质金属蛋白酶9 (MMP9)/S100A10/b.End3

Key words

Lentivirus vector/MMP9/S100A10/b.End3

分类

医药卫生

引用本文复制引用

陈雪雯,朱红梅,温海..MMP9、S100A10基因沉默稳转小鼠细胞系的构建及验证[J].中国真菌学杂志,2017,12(1):19-22,18,5.

基金项目

国家自然科学基金(31470252,81271800,31270181) (31470252,81271800,31270181)

中国真菌学杂志

OACSCDCSTPCD

1673-3827

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