| 注册
首页|期刊导航|中华医学杂志(英文版)|Adenovirus-mediated overexpression of novel mutated IκBα inhibits nuclear factor κB activation in endothelial cells

Adenovirus-mediated overexpression of novel mutated IκBα inhibits nuclear factor κB activation in endothelial cells

ZHOU Lin-fu YIN Kai-sheng ZHU Zi-lu ZHU Yi YAO Xin MAO Hui XIE Wei-ping HUANG Mao

中华医学杂志(英文版)2005,Vol.118Issue(17):1422-1428,7.
中华医学杂志(英文版)2005,Vol.118Issue(17):1422-1428,7.

Adenovirus-mediated overexpression of novel mutated IκBα inhibits nuclear factor κB activation in endothelial cells

Adenovirus-mediated overexpression of novel mutated IκBα inhibits nuclear factor κB activation in endothelial cells

ZHOU Lin-fu 1YIN Kai-sheng 1ZHU Zi-lu 2ZHU Yi 1YAO Xin 1MAO Hui 1XIE Wei-ping 1HUANG Mao1

作者信息

  • 1. Department of Respiratory Medicine, First Affiliated Hospital, Nanjing Medical University, Nanjing 210029, China
  • 2. Department of Biochemistry and Molecular Biology, Nanjing Medical University, Nanjing 210029, China
  • 折叠

摘要

Abstract

Background Nuclear factor κB (NF-κB) overactivation, requiring phosphorylation and degradation of its inhibitor IκBα, is the basis for chronicity of airway inflammation in asthma. Based on our previous plasmid pShuttle-IκBα, carrying an IκBα gene from human placenta, we optimized a novel IκBα mutant (IκBαM) gene, constructed and characterized its replication-deficient recombinant adenovirus (AdIκBαM), and tested whether AdIκBαM-mediated overexpression of IκBαM could inhibit the NF-κB activation in endothelial cells. Methods IκBαM gene (203-1003 bp) encoding 267 amino acids, acquired by site-directed deleting N-terminal phosphorylation sites of serine 32/36, was subcloned into the pShuttle and pGEM-T vectors for further polymerase chain reaction (PCR), restriction digestion, deoxyribonucleic acid (DNA) sequencing and homology analyses. Subsequent to inserting the expression unit of pShuttle-IκBαM, containing cytomegalovirus (CMV) promoter, IκBαM complementary DNA (cDNA) and polyadenylic acid (PolyA) signals, into the type 5 adenovirus (Ad5) vector, the resultant AdIκBαM was packaged in human embryonic kidney (HEK) 293 cells by cotransfection with lipofectamine. Western blot analysis and electrophoretic mobility shift assay were utilized to detect the AdIκBαM-mediated overexpression of IκBαM in HEK293 cells and its suppressive effect on phorbol 12-myristate 13-acetate (PMA)-induced NF-κB activation in human umbilical vein endothelial (ECV304) cells, respectively. Results The relevant nucleotides and deduced amino acids of 801 bp IκBαM gene were consistent with those of IκBα gene (GenBank accession number: M69043). The titer of the prepared AdIκBαM was 4.0×1012 plaque-forming units (pfu)/L. Moreover, the IκBαM gene was overexpressed in HEK293 cells, and potently inhibited the PMA-induced NF-κB activation in ECV304 cells dose-dependently. Conclusions AdIκBαM is a novel vector for both efficient transfer and specific overexpression of IκBαM gene, as well as potent inhibition of NF-κB activity, providing a promising strategy for gene therapy of asthma.

关键词

IκBα mutant/nuclear factor κB/recombinant adenovirus/gene therapy/asthma

Key words

IκBα mutant/nuclear factor κB/recombinant adenovirus/gene therapy/asthma

分类

医药卫生

引用本文复制引用

ZHOU Lin-fu,YIN Kai-sheng,ZHU Zi-lu,ZHU Yi,YAO Xin,MAO Hui,XIE Wei-ping,HUANG Mao..Adenovirus-mediated overexpression of novel mutated IκBα inhibits nuclear factor κB activation in endothelial cells[J].中华医学杂志(英文版),2005,118(17):1422-1428,7.

基金项目

This study was supported by grants from the National Youth Natural Science Foundation of China (No. 30400191) and the Key Subject of '135' Project of Jiangsu Province (No. 20013102). (No. 30400191)

中华医学杂志(英文版)

OAMEDLINESCI

0366-6999

访问量3
|
下载量0
段落导航相关论文