Macrophage and foam cell release of matrix-bound growth factors: Role of plasminogen activation Journal Article


Authors: Falcone, D. J.; McCaffrey, T. A.; Haimovitz-Friedman, A.; Vergilio, J. A.; Nicholson, A. C.
Article Title: Macrophage and foam cell release of matrix-bound growth factors: Role of plasminogen activation
Abstract: We have determined whether macrophage derived-foam cells, a prominent component of the atherosclerotic lesion, express more urokinase-type plasminogen activator (uPA) and whether their ability to generate plasmin stimulates the.release of matrix-bound growth factors. Steady state levels of uPA mRNA and both membrane and intracellular uPA activities were significantly increased in foam cells. When cultured on cell-derived matrices containing bound I-125-basic fibroblast growth factor (bFGF), both macrophage and foam cells released intact I-125-bFGF into their media. The release of I-125-bFGF by either cell was significantly enhanced in the presence of plasminogen. However, foam cells, which expressed more membrane uPA, released more I-125-bFGF than control cells. The release of matrix-bound bFGF was independent of heparanase activity, since neither macrophage nor foam cells degraded (SO4)-S-35-labeled heparan sulfate proteoglycans. In addition, media derived from foam cells cultured on cell-derived matrices in the presence of plasminogen had increased levels of transforming growth factor (TGF) beta activity as compared to cells grown in the absence of plasminogen. In contrast, plasminogen had no effect on TGF-beta activity recovered in the media of foam cells grown on plastic. Moreover, when macrophage were cultured on matrices containing bound I-125-TGF-beta, the release of labeled TGF-beta was increased in the presence of plasminogen. This is the first demonstration that foam cells can release two important growth regulators, bFGF and TGF-beta, from the extracellular matrix, and provides a mechanism by which macrophage and foam cells can stimulate atherosclerotic lesion development.
Keywords: lesions; basement-membranes; lipoproteins; factor-beta; low-density; urokinase-type; smooth-muscle cells; capillary endothelial-cells; atherosclerotic; subendothelial extracellular-matrix; human monocyte-macrophages; factor-like protein
Journal Title: Journal of Biological Chemistry
Volume: 268
Issue: 16
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 1993-06-05
Start Page: 11951
End Page: 11958
Language: English
ACCESSION: WOS:A1993LF28400074
PROVIDER: wos
PUBMED: 8505319
Notes: Article -- Source: Wos
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