4.6 Article

Absence of αvβ6 integrin is linked to initiation and progression of periodontal disease

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 172, Issue 5, Pages 1271-1286

Publisher

AMER SOC INVESTIGATIVE PATHOLOGY, INC
DOI: 10.2353/ajpath.2008.071068

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Integrin alpha v beta 6 is generally not expressed in adult epithelia but is induced in wound healing, cancer, and certain fibrotic disorders. Despite this generalized absence, we observed that alpha v beta 6 integrin is constitutively expressed in the healthy junctional epithelium linking the gingiva to tooth enamel. Moreover, expression of alpha v beta 6 integrin was down-regulated in human periodontal disease, a common medical condition causing tooth loss and also contributing to the development of cardiovascular diseases by increasing the total systemic inflammatory burden. Remarkably, integrin beta 6 knockout mice developed classic signs of spontaneous, chronic periodontal disease with characteristic inflammation, epithelial down-growth, pocket formation, and bone loss around the teeth. Integrin alpha v beta 6 acts as a major activator of transforming growth factor-beta 1 (TGF-beta 1), a key anti-inflammatory regulator in the immune system. Co-expression of TGF-beta 1 and alpha v beta 6 integrin was observed in the healthy junctional epithelium. Moreover, an antibody that blocks alpha v beta 6 integrin-mediated activation of TGF-beta 1 initiated inflammatory periodontal disease in a rat model of gingival inflammation. Thus, alpha v beta 6 integrin is constitutively expressed in the epithelium sealing the gingiva to the tooth and plays a central role in protection against inflammatory periodontal disease through activation of TGF-beta 1.

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