Lee S-I, Kim G-T, Kim H J, Park S-H, Kim E-C
Department of Dental Hygiene, School of Health Science, Dankook University, Cheonan, Republic of Korea Department of Oral and Maxillofacial Pathology, School of Dentistry and Research Center for Tooth and Periodontal Regeneration (MRC), Kyung Hee University, Seoul, Republic of Korea.
Department of Oral and Maxillofacial Radiology, School of Dentistry, Kyung Hee University, Seoul, Republic of Korea.
J Dent Res. 2014 Jul;93(7):678-84. doi: 10.1177/0022034514535214. Epub 2014 May 12.
The precise regulation of odontoblast differentiation and osteoclastogenic cytokine expression in human dental pulp cells (HDPCs) is crucial for the pathology of bacteria-related pulpitis. Although the up-regulation of nucleotide-binding oligomerization domain-containing protein 2 (NOD2) has been reported in inflamed human dental pulps, the role of NOD2 in the differentiation of HDPCs remains unclear. Here, we show the involvement of NOD2 in odontoblast differentiation together with osteoclastogenic cytokine expression in HDPCs. Treatment with muramyl dipeptide (MDP), a known NOD2-agonist, significantly inhibited odontoblast differentiation of HDPCs, as revealed by reduced ALP activity, osteoblast/odontoblast marker expression, and mineralized nodule formation. Importantly, the forced down-regulation of NOD2 by small interfering RNA (siRNA) recovered MDP-down-regulated odontoblast differentiation. MDP-elicited suppression of odontoblast differentiation resulted from the increased expression of MKP-1 protein and the subsequent decline of MAPKs phosphorylation, which is a prerequisite for odontoblast differentiation. Furthermore, we found that MDP treatment elevated the expression of osteoclastogenic cytokines in HDPCs, which was also reversed by NOD2 silencing. Analysis of these data, taken together, suggests that the regulation of NOD2 expression upon MDP challenge might serve as an intrinsic mechanism that underlies the hindered dentin formation and accelerated dentin resorption in bacterial infection-mediated pulpitis.
人牙髓细胞(HDPCs)中牙本质细胞分化和成骨细胞生成细胞因子表达的精确调控对于细菌相关性牙髓炎的病理过程至关重要。尽管在发炎的人牙髓中已报道含核苷酸结合寡聚化结构域蛋白2(NOD2)上调,但NOD2在HDPCs分化中的作用仍不清楚。在此,我们展示了NOD2参与HDPCs中牙本质细胞分化以及成骨细胞生成细胞因子表达。用已知的NOD2激动剂胞壁酰二肽(MDP)处理,显著抑制了HDPCs的牙本质细胞分化,这通过碱性磷酸酶(ALP)活性降低、成骨细胞/牙本质细胞标志物表达减少以及矿化结节形成得以揭示。重要的是,通过小干扰RNA(siRNA)强制下调NOD2可恢复MDP下调的牙本质细胞分化。MDP引发的牙本质细胞分化抑制是由于MKP-1蛋白表达增加以及随后丝裂原活化蛋白激酶(MAPKs)磷酸化水平下降所致,而MAPKs磷酸化是牙本质细胞分化的先决条件。此外,我们发现MDP处理可提高HDPCs中成骨细胞生成细胞因子的表达,NOD2沉默也可使其逆转。综合分析这些数据表明,MDP刺激后NOD2表达的调控可能是细菌感染介导的牙髓炎中牙本质形成受阻和牙本质吸收加速的内在机制。