Involvement of MT1-MMP and TIMP-2 in human periodontal disease

Oral Dis. 2010 May;16(4):388-95. doi: 10.1111/j.1601-0825.2009.01651.x. Epub 2010 Mar 9.

Abstract

Objectives: 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 periodontitis-affected gingival tissues. The altered balance between these two molecular mediators of collagen remodeling suggests their involvement in human periodontal disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Gingiva / enzymology*
  • Gingiva / pathology
  • Humans
  • Immunohistochemistry
  • Matrix Metalloproteinase 14 / metabolism*
  • Periodontitis / enzymology*
  • Periodontitis / pathology
  • Reference Values
  • Tissue Inhibitor of Metalloproteinase-2 / metabolism*

Substances

  • Tissue Inhibitor of Metalloproteinase-2
  • Matrix Metalloproteinase 14