EZH2 regulates dental pulp inflammation by direct effect on inflammatory factors

被引:25
|
作者
Hui, Tianqian [1 ,2 ,3 ]
Peng, A. [1 ]
Zhao, Yuan [1 ]
Yang, Jing [1 ]
Ye, Ling [1 ]
Wang, Chenglin [1 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, State Key Lab Oral Dis, 14 Sect 3,Renmin South Rd, Chengdu 610041, Sichuan, Peoples R China
[2] Peking Univ Sch, Peking Univ Sch, Dept Pediat Dent, Beijing, Peoples R China
[3] Peking Univ, Hosp Stomatol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
EZH2; Dental pulp inflammation; Inflammatory factors; Chemokines; Interleukins; VERSUS-HOST-DISEASE; NF-KAPPA-B; IN-VITRO; INTERFERON-GAMMA; IMMUNE-RESPONSE; CELLS; EXPRESSION; DIFFERENTIATION; PROLIFERATION; PROTEIN;
D O I
10.1016/j.archoralbio.2017.10.004
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Pulpitis is a multi-factorial disease that could be caused by complex interactions between genetics, epigenetics and environmental factors. We aimed to evaluate the role of Enhancer of Zeste Homolog 2 (EZH2) in the inflammatory response of human dental pulp cells (HDPCs) and dental pulp tissues. Methods: The expressions of inflammatory cytokines in HDPCs treated by EZH2 complex or EZH2 siRNA with or without rhTNF-alpha were examined by quantitative real-time polymerase chain reaction (q-PCR). The levels of secreted inflammatory cytokines including IL-6, IL-8, IL-15, CCL2 and CXCL12 in culture supernatants were measured by Luminex assay. In rat pulpitis model, the effects of EZH2 on dental pulp tissues were verified by histology. We invested the mechanisms of the effect of EZH2 on the inflammatory factors by ChIP assay. Results: EZH2 down-regulation inhibited the expression of inflammatory factors, including IL-6, IL-8, IL-15, CCL2 and CXCL12 in HDPCs. EZH2 complex promoted the expression and secretion of these inflammatory factors in HDPCs, while EZH2 silencing could attenuate the promotion of inflammatory factors that were induced by rhTNF-a. In pulpitis models of rats, EZH2 down-regulation inhibited the inflammatory process of dental pulp while EZH2 complex showed no significant facilitation of pulpal inflammation. In addition, EZH2 could bind on the promoters of IL-6, IL-8 and CCL2, but not IL-15 and CXCL12, to affect the transcription of these proinflammatory cytokines. Conclusions: In HDPCs, EZH2 could induce inflammation, while EZH2 down-regulation could attenuate the inflammatory responses. EZH2 plays an important role in this inflammatory process of dental pulp.
引用
收藏
页码:16 / 22
页数:7
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