<i>Porphyromonas gingivalis</i> enhances the senescence-induced increase of 5-alpha reductase in gingival fibroblasts
- 1. Ataturk Univ, Fac Dent, Dept Periodontol, Erzurum, Turkiye
- 2. Ataturk Univ, Fac Med, Dept Biostat, Erzurum, Turkiye
Description
Objectives Aging is characterized by chronic inflammatory activity. Senescent cells increase with chronic inflammation and age-related pathologies, including periodontal disease. As a critical regulator of tissue inflammaging, we hypothesized that 5a reductase (5 alpha R) is associated with periodontal disease and bacteria-induced senescence in gingival fibroblasts.
Materials and methods We recruited 36 patients with periodontitis, measured 5 alpha R immunohistochemically before and after periodontal treatment, and compared the expression of 5aR in gingival biopsies from 12 healthy individuals. We then tested the impact of Porphyromonas gingivalis on gingival fibroblasts treated with or without D-galactose-induced cell senescence. We treated primary gingival fibroblasts with D-galactose-supplemented media (0 mu M, 50 mu M, 100 mu M, 1 mM, 10 mM, 50 mM) to induce senescence. The expression of type 1 and type 2 5 alpha R was analyzed with real-time PCR and immunocytochemistry. The levels of IL-6, IL-8, TNF-alpha, and MCP-1 in fibroblast cultures were evaluated by multiplex immunoassay.
Results In gingival biopsies from patients with periodontal disease, the expression of 5aR was significantly higher than in samples from individuals without periodontal disease (p < 0.001). Periodontal treatment significantly reduced the expression of 5aR in gingival tissues (p < 0.001) to levels comparable in healthy individuals. Gingival fibroblasts exposed to D-galactose-supplemented media had a dose-dependent and significant increase in 5 alpha R expression (p < 0.001). P. gingivalis caused statistically higher type 1 and type 2 5aR expression in gingival fibroblast cells. This effect was exacerbated by the lower doses of D-galactose (p = 0.037). Cells infected with P. gingivalis produced significantly higher levels of IL-6, IL-8, TNF-alpha, and MCP-1 (p < 0.05) regardless of the D-galactose exposure.
Conclusion The results suggested that 5aR plays a role in periodontal disease and mediates the senescence-induced response to P. gingivalis in gingival fibroblasts.
Clinical relevance Periodontal diseases and aging can increase the production of 5-alpha reductase in the gingival tissue.
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