IFN-gR2 is strongly expressed on endothelial cells of gingival tissues from patients with chronic periodontitis

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Abstract

Chronic periodontitis (CP) is characterized by gingival inflammation and bone destruction. It has been reported that interferon-gamma (IFN-g) levels are high in CP patients; however, the IFN-g receptor (IFN-gR) has not been studied in gingival tissue from these patients. Objective: To evaluate IFN-g levels and IFN-gR expression in gingival tissue biopsies from chronic periodontitis patients compared with healthy subjects (HS). Material and Methods: Gingival tissues were obtained from all study subjects, CP (n=18) and healthy subjects (HS) (n=12). A tissue section of each study subject was embedded in paraffin blocks to determine the expression of IFN-g R (IFN-gR1 and IFN-gR2) through immunohistochemistry. Another section of the tissue was homogenized and IFN-g was measured by the ELISA technique. Results: No significant differences were found in the IFN-gR1 expression within the cell layers of the gingival tissue of the study groups. When analyzing the IFN-gR2 expression it was found that IFN-gR2 is strongly expressed in the endothelial cells of CP patients when compared to HS (p<0.05). IFN-g concentrations in the gingival tissue were significantly higher in CP patients than in HS. No significant correlation between IFN-g levels and the expression of IFN-gR1 and IFN-gR2 was found. However, a positive correlation between IFN-g levels and clinical parameters [probing depth (PD) and clinical attachment level (CAL)] was found. Conclusion: The study of IFN-gR expression in gingival tissue samples from patients with CP showed an increase only in the IFN-gR2 chain in endothelial cells when compared to HS.

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Franco-Topete, R., Zepeda-Nuño, J. S., Zamora-Perez, A. L., Fuentes-Lerma, M. G., Gómez-Meda, B. C., & Guerrero-Velázquez, C. (2018). IFN-gR2 is strongly expressed on endothelial cells of gingival tissues from patients with chronic periodontitis. Journal of Applied Oral Science, 26. https://doi.org/10.1590/1678-7757-2017-0291

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