論文

査読有り
2002年4月

Plasmid DNA activates murine macrophages to induce inflammatory cytokines in a CpG motif-independent manner by complex formation with cationic liposomes

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
  • K Yasuda
  • ,
  • Y Ogawa
  • ,
  • M Kishimoto
  • ,
  • T Takagi
  • ,
  • M Hashida
  • ,
  • Y Takakura

293
1
開始ページ
344
終了ページ
348
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/S0006-291X(02)00210-3
出版者・発行元
ACADEMIC PRESS INC ELSEVIER SCIENCE

Plasmid DNA (pDNA) is very important in non-viral gene therapy and DNA vaccination. Unmethylated CpG motifs in bacterial DNA, but not in vertebrate DNA, are known to trigger an inflammatory response, which inhibits gene expression while improving immunological consequences. In this report, we investigated the cytokine secretion induced by pDNA/cationic liposome complexes using murine macrophages. Naked CpG DNA induced tumor necrosis factor-alpha (TNF-alpha) secretion from the macrophages. but DNA without CpG motif did not, demonstrating that the cytokine induction was mediated by CpG motifs. pDNA complexed with cationic liposomes, but not the cationic liposomes alone, produced a significant amount of TNF-alpha from the macrophages. Surprisingly, methylated pDNA and calf thymus DNA complexed with the cationic liposomes were also able to induce TNF-alpha production, indicating that these responses were not dependent on CpG motifs. Taken together, the present study demonstrated that for the first time DNA can stimulate murine macrophages in a CpG motif-independent manner when it is complexed with the cationic liposomes. (C) 2002 Elsevier Science (USA). All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/S0006-291X(02)00210-3
J-GLOBAL
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=200902139978255051
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/12054606
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000175514700053&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/S0006-291X(02)00210-3
  • ISSN : 0006-291X
  • J-Global ID : 200902139978255051
  • PubMed ID : 12054606
  • Web of Science ID : WOS:000175514700053

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