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Expression of protease‐activated receptor‐1 and ‐2 in orofacial granulomatosis
Author(s) -
Ketabchi S,
Massi D,
Ficarra G,
Rubino I,
Franchi A,
Paglierani M,
Simoni A,
Capodiferro S,
Favia G,
Maiorano E,
Tarantini F,
Cirino G,
Santucci M
Publication year - 2007
Publication title -
oral diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.953
H-Index - 87
eISSN - 1601-0825
pISSN - 1354-523X
DOI - 10.1111/j.1601-0825.2006.01317.x
Subject(s) - pathology , immunohistochemistry , medicine , proinflammatory cytokine , histiocyte , immunostaining , lesion , oral mucosa , inflammation , immunology
Objective: Orofacial granulomatosis (OFG) is a rare condition characterized by non‐caseating granulomas in the orofacial region. Protease‐Activated Receptors (PARs) play a role in inflammatory diseases in diverse human tissues. The aim of the study was to investigate the expression of PAR‐1, PAR‐2, MMP‐2, MMP‐9, COX‐1, and COX‐2 in tissues taken from OFG patients. Methods: PAR‐1, PAR‐2, MMP‐2, MMP‐9, COX‐1, and COX‐2 expression was evaluated by immunohistochemistry in biopsies taken from oral Crohn's disease (five cases), Melkersson–Rosenthal syndrome (MRS) (six cases), cheilitis granulomatosa (five cases) and normal oral mucosa (five cases). Results: PAR‐1 was observed in mononuclear inflammatory cells in edematous/lichenoid lesions, whereas a strong PAR‐2 immunostaining was detected in epithelioid histiocytes and giant cells in granulomatous lesions, irrespective of the clinical features (Crohn vs MRS). MMPs and COX‐2 were expressed in the inflammatory component of edematous/lichenoid lesions and markedly overexpressed in granulomatous lesions. COX‐1 was weakly and variably expressed in both edematous/lichenoid and granulomatous lesions. Conclusion: Thus, PAR‐1 and PAR‐2 expressions were related to the intensity and type of inflammatory response but not to the type of clinical lesion. Simultaneous overexpression of PARs, MMPs and COXs suggests synergism among these proinflammatory receptors and enzymes.