[HTML][HTML] Matrix metalloproteinases regulate neovascularization by acting as pericellular fibrinolysins

N Hiraoka, E Allen, IJ Apel, MR Gyetko, SJ Weiss - Cell, 1998 - cell.com
N Hiraoka, E Allen, IJ Apel, MR Gyetko, SJ Weiss
Cell, 1998cell.com
During angiogenesis, endothelial cells penetrate fibrin barriers via undefined proteolytic
mechanisms. We demonstrate that the fibrinolytic plasminogen activator (PA)-plasminogen
system is not required for this process, since tissues isolated from PA-or plasminogen-
deficient mice successfully neovascularize fibrin gels. By contrast, neovessel formation, in
vitro and in vivo, is dependent on fibrinolytic, endothelial cell-derived matrix
metalloproteinases (MMP). MMPs directly regulate this process as invasion-incompetent …
Abstract
During angiogenesis, endothelial cells penetrate fibrin barriers via undefined proteolytic mechanisms. We demonstrate that the fibrinolytic plasminogen activator (PA)-plasminogen system is not required for this process, since tissues isolated from PA- or plasminogen-deficient mice successfully neovascularize fibrin gels. By contrast, neovessel formation, in vitro and in vivo, is dependent on fibrinolytic, endothelial cell-derived matrix metalloproteinases (MMP). MMPs directly regulate this process as invasion-incompetent cells penetrate fibrin barriers when transfected with the most potent fibrinolytic metalloproteinase identified in endothelium, membrane type-1 MMP (MT1-MMP). Membrane display of MT1-MMP is required, as invasion-incompetent cells expressing a fibrinolytically active, transmembrane-deleted form of MT1-MMP remain noninvasive. These observations identify a PA-independent fibrinolytic pathway wherein tethered MMPs function as pericellular fibrinolysins during the neovascularization process.
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