Helicobacter pylori inhibited cell proliferation in human periodontal ligament fibroblasts through the cdc25c/CDK1/cyclinB1 signaling cascade

被引:6
|
作者
Li, Huanying [1 ]
Liang, Dongsheng [1 ]
Hu, Naiming [1 ]
Dai, Xingzhu [1 ]
He, Jianing [1 ]
Zhuang, Hongmin [1 ]
Zhao, Wanghong [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Stomatol, 1838 Guangzhou Ave North, Guangzhou 510630, Guangdong, Peoples R China
来源
JOURNAL OF PERIODONTAL AND IMPLANT SCIENCE | 2019年 / 49卷 / 03期
关键词
Cell cycle; Cell proliferation; Helicobacter pylori; Periodontal ligament; Periodontitis; POLYMERASE-CHAIN-REACTION; DENTAL PLAQUE; BACTERIA; INVASION; SALIVA;
D O I
10.5051/jpis.2019.49.3.138
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: Several studies have shown that the oral cavity is a secondary location for Helicobacter pylori colonization and that H. pylorus associated with the severity of periodontitis. This study investigated whether H.pylori had an effect on the periodontium. We established an invasion model of a standard strain of H.pylori in human periodontal ligament fibroblasts (hPDLFs), and evaluated the effects of H. pylori on cell proliferation and cell cycle progression. Methods: Different concentrations of H. pylori were used to infect hPDLFs, with 6 hours of co-culture. The multiplicity of infection in the low- and high-concentration groups was 10:1 and 100:1, respectively. The Cell Counting Kit-8 method and Ki-67 immunofluorescence were used to detect cell proliferation. Flow cytometry, quantitative real-time polymerise chain reaction, and western blots were used to detect cell cycle progression. In the high-concentration group, the invasion of H. pylori was observed by transmission electron microscopy. Result: It was found that H. pylori invaded the fibroblasts, with cytoplasmic localization. Analyses of cell proliferation and flow cytometry showed that H. pylori inhibited the proliferation of periodontal fibroblasts by causing G2 phase arrest. The inhibition of proliferation and G2 phase arrest were more obvious in the high-concentration group. In the low-concentration group, the G2 phase regulatory factors cyclin dependent kinase 1 (CDK1) and cell division cycle 25C (Cdc2SC) were upregulated, while cyclin B1 was inhibited. However, in the high-concentration group, cyclin B1 was upregulated and CDK1 was inhibited. Furthermore, the deactivated states of tyrosine phosphorylation ofCDK1 (CDK1-Y15) and serine phosphorylation of Cdc25C (Cdc25C-S216) were upregulated after H. pylori infection. Conclusions: In our model, H. pylori inhibited the proliferation of hPDLFs and exerted an invasive effect, causing G2 phase arrest via the Cdc2SC/CDK1/cyclin B1 signaling cascade. Its inhibitory effect on proliferation was stronger in the high-concentration group.
引用
收藏
页码:138 / 147
页数:10
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