Influence of titanium on in vitro fibroblast-Porphyromonas gingivalis interaction in peri-implantitis

被引:45
作者
Irshad, Muhammad [1 ,2 ]
Scheres, Nina [1 ,2 ]
Crielaard, Wim [1 ,2 ]
Loos, Bruno G. [2 ,3 ]
Wismeijer, Daniel [2 ,4 ]
Laine, Marja L. [2 ,3 ]
机构
[1] Univ Amsterdam, Acad Ctr Dent Amsterdam ACTA, Dept Prevent Dent, NL-1081 LA Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Amsterdam, Netherlands
[3] Univ Amsterdam, ACTA, Dept Periodontol, NL-1081 LA Amsterdam, Netherlands
[4] Univ Amsterdam, ACTA, Res Inst MOVE, Dept Oral Funct & Restorat Dent,Sect Oral Implant, NL-1081 LA Amsterdam, Netherlands
关键词
biomaterial; cytokines; fibroblast; inflammation; Porphyromonas gingivalis; 3-YEAR CLINICAL-TRIAL; SHAPED ORAL IMPLANTS; TISSUE-RESPONSE; RESECTIVE SURGERY; IMMUNE-RESPONSE; DENTAL IMPLANTS; CYTOKINE LEVELS; WEAR-PARTICLES; PURE TITANIUM; DISEASES;
D O I
10.1111/jcpe.12136
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aim: Titanium wear particles have been found in peri-implant tissues, but their role in the pathogenesis of peri-implantitis remains unclear. We aimed to determine the in vitro inflammatory responses of peri-implant granulation tissue fibroblasts (PIGFs) to titanium particles alone and in the presence of viable Porphyromonas gingivalis. Materials & Methods: Peri-implant granulation tissue fibroblasts were challenged either with TiO2 particles, P. gingivalis or a combination of TiO2 particles and P. gingivalis. Gene expression and protein production of pro-inflammatory mediators by PIGFs were measured with PCR and ELISA, respectively. Results: Higher doses of TiO2 were toxic to PIGFs and in sub-toxic doses, TiO2 caused an increase in gene expression of tumour necrosis factor (TNF)-A and increased protein production of TNF-alpha, interleukin (IL)-6 and IL-8. A challenge with P. gingivalis alone induced gene expression of TNF-A, IL-1, IL-6 and IL-8. A combined challenge with TiO2 and P. gingivalis caused a stronger increase in gene expression of TNF-A and protein production of TNF-alpha and MCP-1 than P. gingivalis alone. Conclusions: TiO2 particles and P. gingivalis, individually, can induce pro-inflammatory responses in PIGFs. Furthermore, TiO2 particles and viable P. gingivalis further enhance gene expression and production of TNF-alpha by PIGFs. Therefore, Ti wear particles in the peri-implant tissues in combination with P. gingivalis infection may contribute to the pathogenesis of peri-implantitis by enhancing the inflammation in peri-implant tissues.
引用
收藏
页码:841 / 849
页数:9
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