Immune regulatory functions of human beta-defensin-2 in odontoblast-like cells

被引:39
作者
Dommisch, H.
Winter, J.
Willebrand, C.
Eberhard, J.
Jepsen, S.
机构
[1] Univ Hosp Bonn, Dept Periodontol Operat & Preventat Dent, D-53111 Bonn, Germany
[2] Univ Washington, Dept Oral Biol, Seattle, WA 98195 USA
[3] Univ Hosp Schleswig Holstein, Dept Operat Dent & Periodontol, Kiel, Germany
关键词
cytosolic phospholipase-A-2; human beta-defensins; innate immunity; interleukins; odontoblast-like cells; real-time PCR;
D O I
10.1111/j.0143-2885.2007.01228.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aim To investigate the effects of human beta-defensins on the expression of genes involved in the host immune response of the dental pulp. Methodology Human odontoblast-like cells were cultured in Dulbecco's modified Eagle's medium. Cells were stimulated by recombinant human beta-defensins (rhBDs) up to 4 h. RNA was extracted followed by cDNA synthesis (oligo-(dT)-primer). Samples were analysed by real-time polymerase chain reaction (PCR) technology. Genes of interest were: human beta-defensin-1, -2, interleukin (IL)-6, IL-8, tumour necrosis factor-alpha, cyclooxygenase-2, leukotriene-A4-hydrolase, cytosolic phospholipase-A-2 (cPLA(2)), and dentine sialophosphoprotein. Gene expression of beta-actin served as internal standard for normalizing real-time PCR data. Two-way ANOVA and the paired t-test were applied for comparison of the gene expression. Results In odontoblast-like cells rhBD-2 stimulation led to a down-regulation of the gene expression of hBD-1 (P < 0.05), whilst the mRNA expression of IL-6 (P < 0.05), IL-8 (P < 0.05) and cPLA(2) was increased in response to rhBD-2. Conclusion The results of the present study suggest immune regulatory functions of human beta-defensin-2 in odontoblast-like cells.
引用
收藏
页码:300 / 307
页数:8
相关论文
共 39 条
[1]   BIOLOGY OF MULTIFUNCTIONAL CYTOKINES - IL-6 AND RELATED MOLECULES (IL-1 AND TNF) [J].
AKIRA, S ;
HIRANO, T ;
TAGA, T ;
KISHIMOTO, T .
FASEB JOURNAL, 1990, 4 (11) :2860-2867
[2]   HBD-1 - A NOVEL BETA-DEFENSIN FROM HUMAN PLASMA [J].
BENSCH, KW ;
RAIDA, M ;
MAGERT, HJ ;
SCHULZKNAPPE, P ;
FORSSMANN, WG .
FEBS LETTERS, 1995, 368 (02) :331-335
[3]  
Boyce JA, 2005, CHEM IMMUNOL ALLERGY, V87, P59, DOI 10.1159/000087571
[4]   Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria? [J].
Brogden, KA .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (03) :238-250
[5]   Use of human reconstructed epidermis to analyze the regulation of β-defensin hBD-1, hBD-2, and hBD-3 expression in response to LPS [J].
Chadebech, P ;
Goidin, D ;
Jacquet, C ;
Viac, J ;
Schmitt, D ;
Staquet, MJ .
CELL BIOLOGY AND TOXICOLOGY, 2003, 19 (05) :313-324
[6]   Defensin antimicrobial peptides in the oral cavity [J].
Dale, BA ;
Krisanaprakornkit, S .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2001, 30 (06) :321-327
[7]   Human β-defensin (hBD-1,-2) expression in dental pulp [J].
Dommisch, H ;
Winter, J ;
Açil, Y ;
Dunsche, A ;
Tiemann, M ;
Jepsen, S .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2005, 20 (03) :163-166
[8]   Differential gene expression of human β-defensins (hBD-1, -2, -3) in inflammatory gingival diseases [J].
Dommisch, H ;
Açil, Y ;
Dunsche, A ;
Winter, J ;
Jepsen, S .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2005, 20 (03) :186-190
[9]  
DOMMISCH H, 2007, IN PRESS ADV DENT RE
[10]   S-MUTANS AND CARIES - COMMENT [J].
DONKERSLOOT, JA .
JOURNAL OF THE AMERICAN DENTAL ASSOCIATION, 1974, 88 (03) :466-467