NOD2 Mediates Odontoblast Differentiation and RANKL Expression

被引:23
作者
Lee, S. -I. [1 ,2 ,3 ]
Kim, G. -T. [4 ]
Kim, H. J. [2 ,3 ]
Park, S. -H. [5 ]
Kim, E. -C. [2 ,3 ]
机构
[1] Dankook Univ, Sch Hlth Sci, Dept Dent Hyg, Cheonan, South Korea
[2] Kyung Hee Univ, Sch Dent, Dept Oral & Maxillofacial Pathol, Seoul, South Korea
[3] Kyung Hee Univ, Sch Dent, Res Ctr Tooth & Periodontal Regenerat MRC, Seoul, South Korea
[4] Kyung Hee Univ, Sch Dent, Dept Oral & Maxillofacial Radiol, Seoul, South Korea
[5] Kyung Hee Univ, Sch Dent, Dept Conservat Dent, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
pulpitis; dental pulp; muramyl dipeptide; osteoclasts; osteoblasts; Map kinase phosphatase 1; DENTAL-PULP CELLS; IN-VITRO; OSTEOCLAST FORMATION; LIPOPOLYSACCHARIDE; OSTEOBLASTS; FIBROBLASTS; CYTOKINES; PROTEINS; BACTERIA; KINASE;
D O I
10.1177/0022034514535214
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
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.
引用
收藏
页码:678 / 684
页数:7
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