Granulocyte colony stimulating factor (G-CSF) regulates neutrophils infiltration and periodontal tissue destruction in an experimental periodontitis

被引:43
|
作者
Zhang, Zheng [1 ,2 ]
Yuan, Wei [3 ]
Deng, Junjie [3 ]
Wang, Danyang [1 ]
Zhang, Tianyi [4 ]
Peng, Li [5 ]
Tian, Huan [1 ]
Wang, Zuomin [1 ]
Ma, Jie [6 ]
机构
[1] Capital Med Univ, Beijing Chao Yang Hosp, Dept Stomatol, 8th Gongti South Rd, Beijing 100020, Peoples R China
[2] Nankai Univ, Tianjin Stomatol Hosp, Hosp Stomatol, Dept Periodontol, 75th Dagu North Rd, Tianjin 300000, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Natl Canc Ctr, State Key Lab Mol Oncol, Natl Clin Res Ctr Canc,Canc Hosp, 17th Panjiayuan Nanli, Beijing 100021, Peoples R China
[4] Shanxi Med Univ, Sch Stomatol, 56th Xinjian South Rd, Taiyuan 030001, Peoples R China
[5] Third Peoples Hosp Datong City, Dept Stomatol, 1th Wenchang Rd, Datong 037008, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Beijing Hosp, Natl Ctr Gerontol, Dept Biotherapy, 1th Dongdan Dahua Rd, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
Periodontitis; Granulocyte colony-stimulating factor; Neutrophils; Immunology; Osteoclasts; LOCALIZED AGGRESSIVE PERIODONTITIS; IMMUNE-RESPONSE; HEALTHY; MEDIATORS; CELLS;
D O I
10.1016/j.molimm.2019.11.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although granulocyte colony-stimulating factor(G-CSF) has pathogenic roles in several immune inflammatory diseases, its role in periodontitis has not been investigated. Here we detected local expression of G-CSF using public datasets in the Gene Expression Omnibus (GEO) database, and immune cell infiltration into gingival tissue was estimated based on single-sample gene set enrichment analysis (ssGSEA). G-CSF expression and neutrophil infiltration were also confirmed by human gingival biopsies analysis. Moreover, anti-G-CSF neutralizing antibody was locally administrated to investigate the effects of G-CSF neutralization on neutrophils infiltration and periodontal tissue destruction in periodontitis mice model. Two public datasets (GSE10334 and GSE16134), which included 424 patients with periodontitis and 133 health controls, were used in the analysis. Markedly increased immune cell infiltration and G-CSF expression in gingival tissues were found in the periodontitis group as compared to the control group. The higher expression of G-CSF was correlated with higher infiltration of immune cells, especially with neutrophil infiltration. Analysis of gingival biopsies further confirmed high neutrophil infiltration and G-CSF expression. In addition, anti-G-CSF antibody-treated mice with periodontitis showed significantly reduced alveolar bone resorption and neutrophil infiltration when compared with periodontitis mice treated with isotype control antibody. Also, anti-G-CSF antibody treatment significantly reduced mRNA expression of CXC chemokines (CXCL1, CXCL2 and CXCL3), interleukin 1 beta (IL-1 beta), IL-6, matrix metalloproteinases 9, receptor activator of nuclear factor kappa B ligand/osteoprotegerin (RANKL/OPG) ratio and osteoclasts number in periodontal tissues. In summary, neutrophil infiltration and G-CSF expression levels were significantly increased in inflamed gingival tissues. G-CSF neutralization in periodontal inflammation could alleviate neutrophil infiltration and periodontal tissue destruction in experimental periodontitis.
引用
收藏
页码:110 / 121
页数:12
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