Activation of nucleotide-binding oligomerization domain-like receptor family pyrin domain containing 6 by Porphyromonas gingivalis regulates programmed cell death in epithelium

被引:1
|
作者
Liu, Jianru
Liu, Wenyi
Lv, Peiying
Wang, Yixiang [1 ,2 ,3 ,4 ]
Ouyang, Xiangying [5 ]
机构
[1] Peking Univ, Sch & Hosp Stomatol, Beijing Key Lab Digital Stomatol, Natl Clin Res Ctr Oral Dis,Natl Engn Lab Digital &, Beijing, Peoples R China
[2] Peking Univ, Sch & Hosp Stomatol, Beijing Key Lab Digital Stomatol,Cent Lab, Natl Clin Res Ctr Oral Dis,Natl Engn Lab Digital &, Beijing, Peoples R China
[3] Peking Univ, Sch & Hosp Stomatol, Natl Engn Lab Digital & Mat Technol Stomatol, Biobank,Natl Clin Res Ctr Oral Dis,Beijing Key Lab, Beijing 100081, Peoples R China
[4] Peking Univ, Sch & Hosp Stomatol, Cent Lab, 22 Zhongguancun South Ave, Beijing 100081, Peoples R China
[5] Peking Univ, Sch & Hosp Stomatol, Dept Periodontol, 22 Zhongguancun South Ave, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
Pathogen recognition receptors; Programmed cell death; Periodontitis; Epithelial cells; Inflammasome; Porphyromonas gingivalis; SPECK-LIKE PROTEIN; INFLAMMATORY CASPASES; APOPTOSIS; FIBROBLASTS; CLEAVAGE; PLATFORM; LPS;
D O I
10.1016/j.jds.2023.05.008
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background/purpose: Gingival epithelial cells form a physiological barrier against bacterial invasion. Programmed cell death (PCD) regulated by pathogen precognition receptors (PRRs) lead to tissue destruction and is closely related to inflammatory diseases. The purpose of this study was to investigate whether nucleotide-binding oligomerization domain-like receptor family pyrin domain containing 6 (NLRP6) expresses in periodontal epithelium and induces PCD of epithelial cells infected by Porphyromonas gingivalis (P. gingivalis), therefore involves in periodontitis. Material and methods: The expression of NLRP6 was detected in periodontal epithelium from human gingival sections and HaCaT cells stimulated by P. gingivalis. NLRP6 was over-expressed by adenovirus infection in HaCaT or knocked down by siRNA in P. gingivalis infected HaCaT, and the cell death was observed by transmission electron microscopy and flow cytometry analysis. In addition, qPCR and Western blot were performed to determine the expression of NLRP6 and the pyroptosis excutors, caspase-1 and gasdermin D. Enzyme-linked immunosorbent assay were performed to detect the secretion of IL-113 and IL-18. Results: NLRP6 was up-regulated in both gingival epithelium of patients with periodontitis and P. gingivalis infected HaCaT. Over-expression of NLRP6 in HaCaT led to caspase-1 dependent pyroptosis. Interestingly, knockdown of NLRP6 with siRNA followed by P. gingivalis stimulation Conclusion: Up-regulation of NLRP6 by P. gingivalis in HaCaT led to pyroptosis, while knocking down NLRP6 inhibited pyroptosis and induced apoptosis, which indicated this PRR may play a crucial role in periodontitis by regulating PCD in periodontal epithelium.
引用
收藏
页码:1867 / 1875
页数:9
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