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Authordc.contributor.authorOyarzún, A. 
Authordc.contributor.authorArancibia, R. es_CL
Authordc.contributor.authorHidalgo Acosta, Rodrigo es_CL
Authordc.contributor.authorPeñafiel, C. es_CL
Authordc.contributor.authorCáceres, M. es_CL
Authordc.contributor.authorGonzález, M. J. es_CL
Authordc.contributor.authorMartínez, J. es_CL
Authordc.contributor.authorSmith, P. C. es_CL
Admission datedc.date.accessioned2010-06-25T14:14:52Z
Available datedc.date.available2010-06-25T14:14:52Z
Publication datedc.date.issued2010
Cita de ítemdc.identifier.citationOral Diseases (2010) 16, 388–395en_US
Identifierdc.identifier.otherdoi:10.1111/j.1601-0825.2009.01651.x
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/123366
Abstractdc.description.abstractOBJECTIVES: Periodontal disease is characterized by an increased collagen metabolism. Although membrane type-1 matrix metalloproteinase (MT1-MMP) plays a critical role in collagen degradation, its involvement in human periodontitis remains to be determined. METHODS: MT1-MMP and TIMP-2 expression and distribution were evaluated in gingival tissue samples derived from 10 healthy and 12 periodontitis-affected human subjects. MT1-MMP and TIMP-2 expression were assessed through Western-blot of tissue homogenates. The main cell types involved in MT1-MMP and TIMP-2 production were evaluated by means of immunohistochemistry. RESULTS: Both MT1-MMP and TIMP-2 were significantly increased in periodontitis-affected gingival tissues when compared to healthy gingiva. Moreover, the balance between MT1-MMP and its inhibitor TIMP-2 was altered in periodontitis-affected tissues, suggesting an imbalance in this proteolytic axis. Immunohistochemistry demonstrated the expression of MT1-MMP in fibroblasts and macrophages in gingival tissues. MT1-MMP was detected in cells in close association with the gingival collagen matrix. TIMP-2 expression was identified in fibroblasts, macrophages and epithelial cells. CONCLUSIONS: Our observations show an increased expression of MT1-MMP and TIMP-2 in periodontitisaffected gingival tissues. The altered balance between these two molecular mediators of collagen remodeling suggests their involvement in human periodontal disease.en_US
Patrocinadordc.description.sponsorshipWe thank the National Fund for Science and Technology from Chile (FONDECYT Nº 1061065, granted to PS) for financing this study.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherJohn Wileyen_US
Keywordsdc.subjectMMPen_US
Títulodc.titleInvolvement of MT1-MMP and TIMP-2 in human periodontal diseaseen_US
Document typedc.typeArtículo de revista


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