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Active matrix metalloproteinase‐2 upregulation in the abdominal skin of patients with direct inguinal hernia
Author(s) -
Pascual Gemma,
Rodríguez Marta,
GómezGil Verónica,
Trejo Cynthia,
Buján Julia,
Bellón Juan Manvel
Publication year - 2010
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1111/j.1365-2362.2010.02364.x
Subject(s) - inguinal hernia , abdominal wall , matrix metalloproteinase , hernia , medicine , pathology , zymography , tissue inhibitor of metalloproteinase , biopsy , surgery
Eur J Clin Invest 2010; 40 (12): 1113–1121 Abstract Background  Prior studies suggest impaired collagen metabolism involving the whole abdominal wall including the skin in patients with abdominal hernia. We compared expression patterns of matrix metalloproteinase‐2 (MMP‐2) and its modulators membrane type‐1‐matrix metalloproteinase (MT‐1 MMP) and tissue inhibitor of metalloproteinase‐2 (TIMP‐2) in the skin of patients with and without primary inguinal hernia. Materials and methods  Skin biopsy specimens from abdominal wall incisions were obtained during surgery from patients with direct inguinal hernia, indirect inguinal hernia or without hernia (controls). MMP‐2, MT‐1 MMP and TIMP‐2 expression were determined using immunocytochemistry and immunoblotting in intact tissue and in cultured fibroblasts isolated from the biopsies. The degradation activity of MMP‐2 was semiquantitatively determined using zymography. Results  Significantly greater active MMP‐2 expression was observed in skin fibroblasts obtained from patients with direct hernia compared with controls. MT1‐MMP expression was directly correlated with MMP‐2 expression with most intense staining produced in patients with direct or indirect inguinal hernia. TIMP‐2, was maximally expressed in the control group, with significantly diminished expression levels recorded in the hernia groups. Conclusions  Our findings indicate active MMP‐2 upregulation in the abdominal skin of patients with direct inguinal hernia. This metalloproteinase plays a role in matrix degradation, weakening the abdominal wall. Skin disorders and previously described transversalis fascia defects in these patients could point to a systemic collagen metabolism abnormality as a risk factor for direct hernia.

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