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Role of TNF-{alpha} and Its Receptors in Pericoronitis

A. Beklen1,2,3, M. Laine1,2, I. Ventä4, T. Hyrkäs4, and Y.T. Konttinen1,5,6,*

1 Department of Medicine/Invärtes medicin, Helsinki University Hospital, Helsinki, Finland;
2 Institute of Biomedicine/Anatomy, University of Helsinki, Helsinki, Finland;
3 Medico-social Centre, Dental Clinic, Bogazici University, Istanbul, Turkey;
4 Finnish Student Health Service, Helsinki, Finland;
5 ORTON Orthopaedic Hospital of the Invalid Foundation, Helsinki, Finland; and
6 COXA Hospital for Joint Replacement, Tampere, Finland



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Figure 1. Tumor necrosis factor-{alpha} (TNF-{alpha}) and its receptors in pericoronitis. (A) TNF-{alpha} is localized in basal and suprabasal cells, basement membrane, monocyte/macrophage-, fibroblast-like, and vascular endothelial cells. Upper and lower inserts: Twice-magnified images of TNF-{alpha}-positive cells in the lamina propria. (B) No staining was detected in the negative control. (C) TNF-R1 in serial tissue sections is localized in monocyte/macrophage- and fibroblast-like cells, and vascular endothelial and basal epithelial cells. Upper and lower inserts: Twice-magnified images of TNF-R1-positive cells in the lamina propria. (D) TNF-R2 in a serial section is localized in monocyte/macrophage-and fibroblast-like cells, and vascular endothelial and basal epithelial cells. Upper and lower inserts: Twice-magnified images of TNF-R2-positive cells in the lamina propria. Scale bar = 200 µm.

 


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Figure 2. TNF-{alpha} and its receptors in healthy control samples. (A) TNF-{alpha} is almost exclusively localized in fibroblast-like cells and vascular endothelial cells. (B) TNF-R1 in a serial section is localized in stromal fibroblast-like cells and vascular endothelial cells. (C,D) Larger magnifications from the same samples but from different areas, showing TNF-{alpha} and TNF-R1 staining, respectively. (E) In a serial section, weak TNF-R2 staining was occasionally found in a few stromal fibroblast- and macrophage-like, vascular endothelial, and basal epithelial cells. Scale bar = 200 µm.

 


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Figure 3. IL-1ß and VCAM-1 in pericoronitis (A,B, respectively) and healthy tissues (C,D, respectively). In pericoronitis (A), IL-1ß was found in fibroblast - and macrophage-like, vascular endothelial, and epithelial cells. (B) VCAM-1 was mainly localized in endothelial cells of the subepithelial blood vessels. In healthy controls (C), most of the IL-1ß-positive cells were vascular endothelial cells. Very few and weakly IL-1ß-positive subepithelial cells were observed in healthy controls. (D) VCAM-1 was rare. Scale bar = 200 µm; inserts were twice-magnified.

 


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Figure 4. Gelatinolytic activities of the cultured tissue supernatants were studied with zymography. (A) Representative results from non-stimulated (–) and TNF-{alpha}-stimulated (+) healthy tissue sample supernatants at 48 hrs. (B) Inflamed tissue without (–) and with (+) TNF-{alpha} blocker showed reverse findings at 48 hrs. Molecular-weight standards (kDa) are marked to the left (7.5% acrylamide separating gel containing 1 mg/mL gelatin).

 





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