Newly Identified CpG ODNs, M5-30 and M6-395, Stimulate Mouse Immune Cells to Secrete TNF-α and Enhance Th1-Mediated Immunity

被引:11
作者
Choi, Sun-Shim [3 ]
Chung, Eunkyung [4 ,5 ]
Jung, Yu-Jin [1 ,2 ]
机构
[1] Kangwon Natl Univ, Dept Biol Sci, Chunchon 200701, South Korea
[2] Kangwon Natl Univ, Med & Biomat Res Ctr, Chunchon 200701, South Korea
[3] Kangwon Natl Univ, Dept Mol & Med Biotechnol, Chunchon 200701, South Korea
[4] Hallym Univ, Dept Biomed Sci, Chunchon 200702, South Korea
[5] Biowells Inc, Chunchon 200702, South Korea
基金
新加坡国家研究基金会;
关键词
TLR; CpG ODN; murine immune system; TNF-alpha; IFN-gamma; TOLL-LIKE RECEPTOR-9; BACTERIAL-DNA; CD40; LIGAND; B-CELLS; ACTIVATION; EXPRESSION; OLIGONUCLEOTIDES; TUBERCULOSIS; INDUCTION; KINASE;
D O I
10.1007/s12275-010-0053-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacterial CpG motifs are known to induce both innate and adaptive immunity in infected hosts via toll-like receptor 9 (TLR9). Because small oligonucleotides (ODNs) mimicking bacterial CpG motifs are easily synthesized, they have found use as immunomodulatory agents in a number of disease models. We have developed a novel bioinformatics approach to identify effective CpG ODN sequences and evaluate their function as TLR9 ligands in a murine system. Among the CpG ODNs we identified, M5-30 and M6-395 showed significant ability to stimulate TNF-alpha and IFN-gamma production in a mouse macrophage cell line and mouse splenocytes, respectively. We also found that these CpG ODNs activated cells through the canonical NF-kappa B signaling pathway. Moreover, both CpG ODNs were able to induce Th1-mediated immunity in Mycobacterium tuberculosis (Mtb)-infected mice. Our results demonstrate that M5-30 and M6-395 function as TLR9-specific ligands, making them useful in the study of TLR9 functionality and signaling in mice.
引用
收藏
页码:512 / 517
页数:6
相关论文
共 28 条
[1]   Recognition of pathogen-associated molecular patterns by TLR family [J].
Akira, S ;
Hemmi, H .
IMMUNOLOGY LETTERS, 2003, 85 (02) :85-95
[2]   Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition [J].
Bauer, S ;
Kirschning, CJ ;
Häcker, H ;
Redecke, V ;
Hausmann, S ;
Akira, S ;
Wagner, H ;
Lipford, GB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9237-9242
[3]   CpG DNA induced IL-12 p40 gene activation is independent of STAT1 activation or production of interferon consensus sequence binding protein [J].
Bradford, M ;
Schroeder, AJ ;
Morse, HC ;
Vogel, SN ;
Cowdery, JS .
JOURNAL OF BIOMEDICAL SCIENCE, 2002, 9 (06) :688-696
[4]  
Chuang TH, 2002, J LEUKOCYTE BIOL, V71, P538
[5]   A comparative analysis of cytokine responses, cell surface marker expression and MAPKs in DCs matured with LPS compared with a panel of TLR ligands [J].
Dowling, David ;
Hamilton, Clare M. ;
O'Neill, Sandra M. .
CYTOKINE, 2008, 41 (03) :254-262
[6]   PI3K is critical for the nuclear translocation of IRF-7 and type IIFN production by human plasmacytoid predendritic cells in response to TLR activation [J].
Guiducci, Cristiana ;
Ghirelli, Cristina ;
Marloie-Provost, Marie-Annick ;
Matray, Tracy ;
Coffman, Robert L. ;
Liu, Yong-Jun ;
Barrat, Franck J. ;
Soumelis, Vassili .
JOURNAL OF EXPERIMENTAL MEDICINE, 2008, 205 (02) :315-322
[7]   CpG oligodeoxynucleotide treatment enhances innate resistance and acquired immunity to African trypanosomes [J].
Harris, Tajie H. ;
Mansfield, John M. ;
Paulnock, Donna M. .
INFECTION AND IMMUNITY, 2007, 75 (05) :2366-2373
[8]   Mechanism and function of a newly identified CpG DNA moth in human primary B cells [J].
Hartmann, G ;
Krieg, AM .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :944-952
[9]   Rational design of new CpG oligonucleotides that combine B cell activation with high IFN-α induction in plasmacytoid dendritic cells [J].
Hartmann, G ;
Battiany, J ;
Poeck, H ;
Wagner, M ;
Kerkmann, M ;
Lubenow, N ;
Rothenfusser, S ;
Endres, S .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (06) :1633-1641
[10]   Toll-like receptors stimulate human neutrophil function [J].
Hayashi, F ;
Means, TK ;
Luster, AD .
BLOOD, 2003, 102 (07) :2660-2669