Abstract | 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.
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Authors | H Dommisch, J Winter, C Willebrand, J Eberhard, S Jepsen |
Journal | International endodontic journal
(Int Endod J)
Vol. 40
Issue 4
Pg. 300-7
(Apr 2007)
ISSN: 0143-2885 [Print] England |
PMID | 17298411
(Publication Type: Journal Article)
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Chemical References |
- DEFB1 protein, human
- DEFB4A protein, human
- DNA, Complementary
- Interleukin-6
- Interleukin-8
- Recombinant Proteins
- beta-Defensins
- Phospholipases A
- Group IV Phospholipases A2
- PLA2G4A protein, human
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Topics |
- Adult
- Analysis of Variance
- Cells, Cultured
- DNA, Complementary
(analysis)
- Dental Pulp
(cytology, immunology)
- Gene Expression Regulation
- Group IV Phospholipases A2
- Humans
- Immunity, Innate
(genetics)
- Interleukin-6
(biosynthesis, genetics, immunology)
- Interleukin-8
(biosynthesis, genetics, immunology)
- Odontoblasts
(immunology)
- Phospholipases A
(biosynthesis, genetics, immunology)
- Polymerase Chain Reaction
- Recombinant Proteins
(pharmacology)
- beta-Defensins
(biosynthesis, genetics, immunology)
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