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Macrophage activation by a DNA/cationic liposome complex requires endosomal acidification and TLR9‐dependent and ‐independent pathways
Author(s) -
Yasuda Kei,
Ogawa Yoshiyuki,
Yamane Ikuko,
Nishikawa Makiya,
Takakura Yoshinobu
Publication year - 2005
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.0204089
Subject(s) - biology , endosome , cationic liposome , tlr9 , macrophage , microbiology and biotechnology , liposome , dna , cationic polymerization , biochemistry , transfection , gene , intracellular , in vitro , gene expression , chemistry , dna methylation , organic chemistry
Previously, we showed that bacterial DNA and vertebrate DNA/cationic liposome complexes stimulate potent inflammatory responses in cultured mouse macrophages. In the present study, we examined whether endocytosis and subsequent acidification are associated with these responses. The endocytosis inhibitor, cytochalasin B, reduced tmor necrosis factor α (TNF‐α) production by a plasmid DNA (pDNA)/cationic liposome complex. The endosomal acidification inhibitor, monensin, inhibited cytokine production by pDNA or a calf thymus DNA/liposome complex. These results suggest, similarly to CpG motif‐dependent responses, that endocytosis and subsequent endosomal acidification are also required for these inflammatory responses. It is intriguing that another inhibitor of endosomal acidification, bafilomycin A, stimulated the production of TNF‐α mRNA and its protein after removal of the pDNA/liposome complex and inhibitors, although it inhibited the release of interleukin‐6. Similar phenomena were observed in the activation of macrophages by CpG oligodeoxynucleotide, calf thymus DNA, and Escherichia coli DNA complexed with liposomes. Moreover, bafilomycin A also induced a high degree of TNF‐α release after stimulation with naked pDNA. These results suggest that bafilomycin A increases TNF‐α production induced by DNA at the transcriptional level via an as‐yet unknown mechanism. Furthermore, we investigated the contribution of Toll‐like receptor 9 (TLR9), the receptor of CpG motifs, to the cell activation by the DNA/cationic liposome complex using the macrophages from TLR9 −/− mice. We observed a reduced inflammatory cytokine release from macrophages of TLR9 −/− mice compared with wild‐type mice. However, the cytokine production was not completely abolished, suggesting that the DNA/cationic liposome complex can induce macrophage activation via TLR9‐dependent and ‐independent pathways.