Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0031099 (periodontitis)
 12,489 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Periodontitis are characterized by the destruction of the extracellular matrix (ECM) of periodontal tissues. Matrix metalloproteinases (MMPs) play an important role in the degradation of ECM. But until now, it is not clear about the regulation of MMPs expression level in periodontitis. EMMPRIN is a 58 kDa, highly glycosylated, transmembrane molecule belonging to the immunoglobin superfamily, which interacts with fibroblasts to stimulate the expression of MMPs. It is logical to postulate that EMMPRIN may play a critical role in the regulation of MMPs participating the destruction of periodontal ECM in periodontitis. The hypothesis will provide the brand-new direction that we may prevent and treat the periodontitis by regulating the expression of EMMPRIN in host aspect.
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PMID:A potential role of EMMPRIN by regulating ECM degradation in periodontitis. 1749 67

Extracellular matrix metalloproteinase inducer (EMMPRIN) or CD147 is a transmembrane glycoprotein expressed by various cell types, including oral epithelial cells. Recent studies have brought evidence that EMMPRIN plays a role in periodontitis. In the present study, we investigated the effect of Porphyromonas gingivalis, a major pathogen in chronic periodontitis, on the shedding of membrane-anchored EMMPRIN and on the expression of the EMMPRIN gene by oral epithelial cells. A potential contribution of shed EMMPRIN to the inflammatory process of periodontitis was analyzed by evaluating the effect of recombinant EMMPRIN on cytokine and matrix metalloproteinase (MMP) secretion by human gingival fibroblasts. ELISA and immunofluorescence analyses revealed that P. gingivalis mediated the shedding of epithelial cell-surface EMMPRIN in a dose- and time-dependent manner. Cysteine proteinase (gingipain)-deficient P. gingivalis mutants were used to demonstrate that both Arg- and Lys-gingipain activities are involved in EMMPRIN shedding. Real-time PCR showed that P. gingivalis had no significant effect on the expression of the EMMPRIN gene in epithelial cells. Recombinant EMMPRIN induced the secretion of IL-6 and MMP-3 by gingival fibroblasts, a phenomenon that appears to involve mitogen activated protein kinases. The present study brought to light a new mechanism by which P. gingivalis can promote the inflammatory response during periodontitis.
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PMID:Porphyromonas gingivalis-mediated shedding of extracellular matrix metalloproteinase inducer (EMMPRIN) by oral epithelial cells: a potential role in inflammatory periodontal disease. 2183 59