Association Between Mast Cells and Collagen Maturation in Chronic Periodontitis in Humans

Mast cells (MCs) can influence the maturation of collagen fibers. This study evaluated the relationship between the distribution and degranulation of MCs and collagen maturation in human gingival tissue in chronic periodontitis. A total of 16 specimens of patients clinically diagnosed as periodontit...

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Published in:The journal of histochemistry and cytochemistry Vol. 66; no. 6; pp. 467 - 475
Main Authors: e Ribeiro, Lívia S.F., dos Santos, Jean N., Rocha, Clarissa A.G., Cury, Patricia R.
Format: Journal Article
Language:English
Published: Los Angeles, CA SAGE Publications 01-06-2018
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Summary:Mast cells (MCs) can influence the maturation of collagen fibers. This study evaluated the relationship between the distribution and degranulation of MCs and collagen maturation in human gingival tissue in chronic periodontitis. A total of 16 specimens of patients clinically diagnosed as periodontitis and 18 controls clinically diagnosed as healthy or gingivitis were included. Immunohistochemistry and Picrosirius staining were performed to identify MCs and assess collagen fibers, respectively. Chi-square, t test, and Pearson’s correlation test (p<0.05) were used. In control specimens, there was a positive association between MCs in the connective tissue and the presence of immature collagen (p=0.001); in periodontitis samples, this association was not confirmed (p≥0.12). There was no significant relationship between periodontal diagnosis and collagen maturation or MC degranulation (p≥0.35). MC density was significantly higher (p=0.04) in periodontitis tissue (339.01 ± 188.94 MCs/mm2) than in control tissue (211.14 ± 131.13 MCs/mm2) in the area of connective tissue containing inflammatory infiltrate. There was a correlation between the number of MCs and probing depth (r = 0.34, p=0.04). MCs are involved in the pathogenesis of periodontal diseases and might be associated with collagen maturation in periodontal tissue during the early stages of periodontal disease pathogenesis.
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ISSN:0022-1554
1551-5044
DOI:10.1369/0022155418765131