CpG DNA-mediated immune response in pulmonary endothelial cells

被引:74
作者
Li, J
Ma, Z
Tang, ZL
Stevens, T
Pitt, B
Li, S
机构
[1] Univ Pittsburgh, Sch Pharm, Ctr Pharmacogenet, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Environm & Occupat Hlth, Pittsburgh, PA 15261 USA
[4] Univ S Alabama, Coll Med, Dept Pharmacol, Ctr Lung Biol, Mobile, AL 36688 USA
关键词
CpG motif; lung;
D O I
10.1152/ajplung.00436.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Although the CpG DNA immune response mediated by Toll-like receptor 9 (TLR9) has been extensively studied in a number of immune cells, the response to CpG DNA in endothelial cells (EC) is not well understood. In this study, we show that both mouse and rat lung EC display constitutive expression of TLR9 mRNA. Exposure to CpG DNA induced a potent proinflammatory response as manifested by an increased expression of IL-8 and ICAM-1 in mouse pulmonary EC. The proinflammatary response was sensitive to chloroquine, consistent with a role of endosomal contribution. A role for p38 MAPK and NF-kappaB pathway was apparent as the response was sensitive to inhibitors of p38 MAPK and NF-kappaB but was not affected by inhibitors of ERK1/2. A synergistic effect of CpG DNA and LPS on the inflammatory response is consistent with multiple TLR interaction in EC. This study suggests a possible role for CpG DNA-mediated EC immune response in the host defense system. It also has important implications in plasmid DNA-mediated pulmonary endothelium gene transfer.
引用
收藏
页码:L552 / L558
页数:7
相关论文
共 37 条
  • [1] Ahn SK, 2003, INT J MOL MED, V12, P231
  • [2] Bacterial DNA evokes epithelial IL-8 production by a MAPK-dependent, NFκB-independent pathway
    Akhtar, M
    Watson, JL
    Nazli, A
    McKay, DM
    [J]. FASEB JOURNAL, 2003, 17 (08) : 1319 - +
  • [3] Recognition of pathogen-associated molecular patterns by TLR family
    Akira, S
    Hemmi, H
    [J]. IMMUNOLOGY LETTERS, 2003, 85 (02) : 85 - 95
  • [4] Ashkar Ali A., 2002, Current Molecular Medicine (Hilversum), V2, P545, DOI 10.2174/1566524023362159
  • [5] Ballas ZK, 1996, J IMMUNOL, V157, P1840
  • [6] Mechanisms of bacterial lipopolysaccharide-induced endothelial apoptosis
    Bannerman, DD
    Goldblum, SE
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2003, 284 (06) : L899 - L914
  • [7] Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition
    Bauer, S
    Kirschning, CJ
    Häcker, H
    Redecke, V
    Hausmann, S
    Akira, S
    Wagner, H
    Lipford, GB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) : 9237 - 9242
  • [8] Diabetes and vascular disease -: Pathophysiology, clinical consequences, and medical therapy:: Part I
    Creager, MA
    Lüscher, TF
    Cosentino, F
    Beckman, JA
    [J]. CIRCULATION, 2003, 108 (12) : 1527 - 1532
  • [9] Toll-like receptor 2 (TLR2) and TLR9 signaling results in HIV-long terminal repeat trans-activation and HIV replication in HIV-1 transgenic mouse spleen cells:: Implications of simultaneous activation of TLRs on HIV replication
    Equils, O
    Schito, ML
    Karahashi, H
    Madak, Z
    Yarali, A
    Michelsen, KS
    Sher, A
    Arditi, M
    [J]. JOURNAL OF IMMUNOLOGY, 2003, 170 (10) : 5159 - 5164
  • [10] Bacterial lipopolysaccharide activates NF-κB through Toll-like receptor 4 (TLR-4) in cultured human dermal endothelial cells -: Differential expression of TLR-4 and TLR-2 in endothelial cells
    Faure, E
    Equils, O
    Sieling, PA
    Thomas, L
    Zhang, FX
    Kirschning, CJ
    Polentarutti, N
    Muzio, M
    Arditi, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) : 11058 - 11063