Expression of caspase-3, p53 and Bcl-2 in generalized aggressive periodontitis

• Published in: Head & face medicine 2006-06, Vol.2 (1), p.17-17, Article 17
• Main Authors: Bulut, Sule, Uslu, Hilal, Ozdemir, B Handan, Bulut, Omer Engin
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aggressive Periodontitis - metabolism; Apoptosis; Biomarkers - metabolism; Biopsy; Case-Control Studies; Caspase 3 - metabolism; Female; Humans; Immunohistochemistry; Male; Proto-Oncogene Proteins c-bcl-2 - metabolism; Tumor Suppressor Protein p53 - metabolism
• ISSN: 1746-160X; 1746-160X
• DOI: 10.1186/1746-160x-2-17

Apoptosis, or programmed cell death is a form of physiological cell death. It is increased or decreased in the presence of infection, inflammation or tissue remodelling. Previous studies suggest that apoptosis is involved in the pathogenesis of inflammatory periodontal disease. The aim of the present study was to investigate the clinical features and known indicators of apoptosis (p53, Bcl-2, Caspase-3) in patients with generalized aggressive periodontitis (GAP) METHODS: Eight patients with GAP, who had sites with probing depths (PD) > 5 mm, and 10 periodontally-healthy persons were included in the study. Clinical examinations and PD were performed, and the plaque index and gingival index were recorded. Gingival tissues biopsies were obtained from active site of each patient and from healthy individuals. The expression of caspase-3, Bcl-2, and p53 was evaluated by immunohistochemistry There were no significant differences between GAP and control group with respect to levels of caspase-3 and p53 expression (P > 0.05). Contrary, the frequency of grade 3 expression of Bcl-2 was higher in GAP group than the control group. The higher frequency of Bcl-2 expression in GAP group indicates and delayed apoptosis can lead to increasing resident inflammatory cells in periodontal tissues and resulting in progressive periodontal destruction.