Paula-Silva F W G, Ghosh A, Silva L A B, Kapila Y L
Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, 1011 N. University Ave., Ann Arbor, MI 48109-1078, USA.
J Dent Res. 2009 Apr;88(4):339-44. doi: 10.1177/0022034509334070.
Dental pulp cells can differentiate toward an odontoblastic phenotype to produce reparative dentin beneath caries lesions. However, the mechanisms involved in pulp cell differentiation under pro-inflammatory stimuli have not been well-explored. Thus, we hypothesized that the pro-inflammatory cytokine tumor necrosis factor-alpha (TNF-alpha) could be a mediator involved in dental pulp cell differentiation toward an odontoblastic phenotype. We observed that TNF-alpha-challenged pulp cells exhibited increased mineralization and early and increased expression of dentin phosphoprotein (DPP), dentin sialoprotein (DSP), dentin matrix protein-1, and osteocalcin during a phase of reduced matrix metalloproteinase (MMP) expression. We investigated whether these events were related and found that p38, a mitogen-activated protein kinase, differentially regulated MMP-1 and DSP/DPP expression and mediated mineralization upon TNF-alpha treatment. These findings indicate that TNF-alpha stimulates differentiation of dental pulp cells toward an odontoblastic phenotype via p38, while negatively regulating MMP-1 expression.
牙髓细胞可向成牙本质细胞表型分化,在龋损下方产生修复性牙本质。然而,促炎刺激下牙髓细胞分化所涉及的机制尚未得到充分研究。因此,我们推测促炎细胞因子肿瘤坏死因子-α(TNF-α)可能是参与牙髓细胞向成牙本质细胞表型分化的介质。我们观察到,在基质金属蛋白酶(MMP)表达降低的阶段,受到TNF-α刺激的牙髓细胞矿化增加,牙本质磷蛋白(DPP)、牙本质涎蛋白(DSP)、牙本质基质蛋白-1和骨钙素的表达提前且增加。我们研究了这些事件是否相关,发现丝裂原活化蛋白激酶p38对MMP-1和DSP/DPP的表达有不同的调节作用,并在TNF-α处理后介导矿化。这些发现表明,TNF-α通过p38刺激牙髓细胞向成牙本质细胞表型分化,同时负向调节MMP-1的表达。