The role of toll‐like and protease‐activated receptors and associated intracellular signaling in Porphyromonas gingivalis‐infected gingival fibroblasts. Issue 2 (February 2017)

• Record Type: Journal Article
• Authors: Palm, Eleonor; Demirel, Isak; Bengtsson, Torbjörn; Khalaf, Hazem
• Is Part Of: Apmis. Volume 125:Issue 2(2017:Feb.)
• Page Start: 157
• Page End: 169
• Publication Date: 2017-02
• Subjects: Porphyromonas gingivalis -- gingival fibroblasts -- protease‐activated receptors -- toll‐like receptors -- cell signaling; Pathology -- Periodicals; Microbiology -- Periodicals; Immunology -- Periodicals; 572
• DOI: 10.1111/apm.12645
• Languages: English
• ISSNs: 0903-4641

Abstract

Abstract : Porphyromonas gingivalis, which is considered a keystone agent in periodontitis, has evolved elaborate mechanisms to grow and survive in a hostile milieu. The gingival fibroblast is the major cell type in the gingiva and is considered to be important in the periodontitis‐associated inflammation. As a part of the innate immune response, they produce cytokines such as CXCL8 and interleukin (IL)‐6 which are believed to contribute to the destruction of the tooth‐supporting tissues. This study investigates how the expression of protease‐activated receptors (PAR1, PAR2) and toll‐like receptors (TLR2, TLR4) changes with P. gingivalis exposure and how silencing of one receptor affects the expression of the other receptors. The importance of protein kinase C (PKC) and p38 in the regulation of CXCL8 and IL‐6 was also examined. Receptors were knockdown with small‐interfering RNA. PKC or p38 was blocked prior to stimulation with P. gingivalis . Fibroblasts were able to compensate for PAR1 knockdown with increased expression of PAR2. PKC and p38 were involved in the regulation of P. gingivalis ‐induced CXCL8 and IL‐6. Our results indicate that PAR1 and PAR2 could be implicated in periodontitis and that PKC and P38 play a role in the inflammatory response in P. gingivalis ‐infected gingival fibroblasts.