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Journal of Dental Research
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Role of NF-{kappa}B in TNF-{alpha}-induced COX-2 Expression in Synovial Fibroblasts from Human TMJ

J. Ke1, X. Long1,2,*, Y. Liu3, Y.F. Zhang4, J. Li2, W. Fang2 and Q.G. Meng2

1 Key Lab. for Oral Biomedical Engineering, Ministry of Education,
2 Departments of Oral Maxillofacial Surgery and
4 Prosthodontics, School & Hospital of Stomatology,
3 Department of Radio-Chemotherapy of Zhongnan Hospital, Wuhan University, Wuhan 430079, PR China


Figure 1
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Figure 1. Dose-dependent TNF-{alpha}-induced COX-2 mRNA and protein in synovial fibroblasts from TMJ. (A) Cells were incubated with various concentrations of TNF-{alpha} for 2 hrs. Total RNA was isolated from cells and analyzed for COX-2 and GAPDH mRNA by RT-PCR. (B) Cells were incubated with various concentrations of TNF-{alpha} for 6 hrs. Whole-cell lysates were prepared and subjected to Western blotting with antibody specific for COX-2 and actin. The data represent 1 of 3 separate experiments with similar results.

 

Figure 2
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Figure 2. Time-dependent TNF-{alpha}-induced COX-2 mRNA and protein in synovial fibroblasts from TMJ. (A) Cells were incubated with 20 ng/mL of TNF-{alpha} for various time intervals. Total RNA was then isolated from cells and analyzed for COX-2 and GAPDH mRNA by RT-PCR. (B) Cells were incubated with 20 ng/mL of TNF-{alpha} for various time intervals, and the whole-cell lysates were prepared and subjected to Western blotting with antibody specific for COX-2 and actin. The data represent 1 of 3 separate experiments with similar results.

 

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Figure 3. Time-course of TNF-{alpha}-induced NF-{kappa}B-specific DNA-protein complex formation and NF-{kappa}B translocation in synovial fibroblasts from TMJ. Cells were treated with 20 ng/mL TNF-{alpha} for various time intervals, and then cytoplasmic and nuclear extracts were prepared. (A) NF-{kappa}B-specific DNA-protein-binding activity in nuclear extracts was determined by EMSA. (B) Supershift assays were performed with specific p65 and p50 antibodies. Moreover, we added unlabeled NF-{kappa}B probes in a 100-fold excess, to determine the specificity of NF-{kappa}B-specific DNA protein. (C) Cytoplasmic and nuclear levels of p65 and p50 proteins were detected by Western blotting. The data represent 1 of 3 separate experiments with similar results.

 

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Figure 4. Inhibitory effect of PDTC on NF-{kappa}B activity and COX-2 protein expression induced by TNF-{alpha} in synovial fibroblasts from the TMJ. (A) NF-{kappa} B binding activity in the nuclear extracts from cells pre-treated with PDTC (50 µmol/L) 1 hr before 20 ng/mL of TNF-{alpha} stimulation for 40 min was determined by EMSA. (B) COX-2 protein expression in the whole-cell lysates from cells pre-treated with PDTC (50 µmol/L) 1 hr before 20 ng/mL of TNF-{alpha} stimulation for 6 hrs was assayed by Western blotting. The data represent 1 of 3 separate experiments with similar results.

 

Journal of Dental Research, Vol. 86, No. 4, 363-367 (2007)
DOI: 10.1177/154405910708600412


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