Experimental Dermatology · 2006 · 34 citations · 47 references
MedicineDermatologyPathologyDermatopathologyImmunopathologyInflammationGranulomatous DermatosesImmunopathology Of SkinInflammatory DermatosesInflammatory Skin DiseasesInflammatory Skin DisordersMacrophage BiologyGranulomatous LesionsGranulomatous Skin InflammationProtein Expression LevelsQuantitative Pcr DetectionQuantitative Polymerase Chain Reaction AssaysSkin FibrosisTransforming Growth Factor Beta RegulationTransforming Growth Factor-beta Signaling
Matrix metalloproteinase (MMP)-21 and MMP-26 (matrilysin-2) are two recently cloned epithelial metalloproteases. Here we examined their expression in various benign skin disorders, in which macrophages and fibroblasts have been implicated as well as in cultures of these cells. Expression of MMP-21 was detected by immunohistochemistry in a subset of macrophages of granulomatous skin lesions and in fibroblasts in dermatofibromas. MMP-21 mRNA was found in THP-1, U937, HEL 299 and Hs68 cells. Furthermore, MMP-21 protein was detected by immunohistochemistry in cultures of the same cell lines. In culture MMP-21 was upregulated by phorbol myristate acetate in THP-1 cells and by retinoic acid (RA) in U937 cells, and downregulated by transforming growth factor beta 1 (TGF-beta1) in HEL 299 as assessed by Taqman quantitative polymerase chain reaction (PCR). Expression of MMP-26 was detected by immunohistochemistry in granulomatous skin diseases and actinic elastosis. MMP-26 at both mRNA and protein levels was only found in HEL 299 cells. In culture it was downregulated by TGF-beta1, RA and IL-1beta as assessed by Taqman quantitative PCR. Our results suggest these two novel MMPs are not only associated with cancer but may be important in connective tissue remodelling and pathobiology of various benign skin disorders.
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Laura Ravanti, Jyrki Heino, Carlos López-Otı́n et al. · Journal of Biological Chemistry · 1999 · 278 citations · Full text