| Literature DB >> 26088424 |
Y L Wang1, H He2, Z J Liu1, Z G Cao1, X Y Wang3, K Yang1, Y Fang1, M Han1, C Zhang1, F Y Huo1.
Abstract
Tumor necrosis factor-α (TNF-α) is involved in various inflammatory processes, including periodontitis. Although the influences of TNF-α on periodontal ligament fibroblasts and osteoblasts have been widely documented, its effects on cementoblasts, the cells responsible for cementum production, remain largely unknown. In this study, we found that TNF-α suppressed the mineralization ability of cementoblasts by inhibiting differentiation and inducing apoptosis. Various signaling pathways, such as p53, PP2AC, p38, Erk1/2, JNK, PI3K-Akt, and NF-κB, were activated during this process. The use of a specific inhibitor and siRNA transfection confirmed that the effects of TNF-α on differentiation and apoptosis in cementoblasts were partially abrogated by inhibiting p53 activity. By contrast, the effects of TNF-α were even exacerbated by the inhibition of the p38, Erk1/2, JNK, PI3K-Akt, and NF-κB pathways. Moreover, p53 activity was further enhanced by blocking the p38, Erk1/2, JNK, and PI3K-Akt signaling pathways. Taken together, these results suggested that the differentiation inhibition and apoptosis in cementoblasts induced by TNF-α were partially dependent on p53 activity. The p38, Erk1/2, JNK, PI3K-Akt, and NF-κB pathways were also activated but acted as balancing players to limit rather than conduct the negative effects of TNF-α. These balancing effects were dependent, or at least partially dependent, on p53, except for the NF-κB pathway. © International & American Associations for Dental Research 2015.Entities:
Keywords: dental cementum; guided tissue regeneration; osterix protein; periodontitis; signal transduction; tumor suppressor protein p53
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Year: 2015 PMID: 26088424 DOI: 10.1177/0022034515590349
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116