Release of cell surface-associated basic fibroblast growth factor by glycosylphosphatidylinositol-specific phospholipase C

• Published in: Journal of cellular physiology Vol. 151; no. 1; p. 126
• Main Authors: Bashkin, P, Neufeld, G, Gitay-Goren, H, Vlodavsky, I
• Format: Journal Article
• Language: English
• Published: United States 01.04.1992
• Subjects: Animals; Cattle; Cell Division - drug effects; Cell Membrane - chemistry; Cell Membrane - metabolism; Cell Membrane - ultrastructure; Cells, Cultured; Endothelium, Vascular - cytology; Endothelium, Vascular - metabolism; Endothelium, Vascular - ultrastructure; Fibroblast Growth Factor 2 - analysis; Fibroblast Growth Factor 2 - metabolism; Fibroblasts - cytology; Fibroblasts - metabolism; Fibroblasts - ultrastructure; Heparitin Sulfate - metabolism; Iodine Radioisotopes; Mice; Mice, Inbred BALB C; Phosphatidylinositol Diacylglycerol-Lyase; Phosphoric Diester Hydrolases - metabolism; Polysaccharide-Lyases - metabolism; Radioligand Assay
• ISSN: 0021-9541
• DOI: 10.1002/jcp.1041510117

Heparan sulfate proteoglycans (HSPG) are ubiquitous constituents of mammalian cell surfaces and most extracellular matrices. A portion of the cell surface HSPG is anchored via a covalently linked glycosyl-phosphatidylinositol (Pl) residue, which can be released by treatment with a glycosyl-Pl specific phospholipase C (Pl-PLC). We report that exposure of bovine aortic endothelial and smooth muscle cells to Pl-PLC resulted in release of cell surface-associated, growth-promoting activity that was neutralized by antibasic fibroblast growth factor (bFGF) antibodies. Active bFGF was also released by treating the cells with bacterial heparitinase. Under the same conditions there was no release of mitogenic activity from cells (BHK-21, NIH/3T3, PF-HR9) that expressed little or no bFGF, as opposed to Pl-PLC-mediated release of active bFGF from the same cells transfected with the bFGF gene. The released bFGF competed with recombinant bFGF in a radioreceptor assay. Addition of Pl-PLC to sparsely seeded vascular endothelial cells resulted in a marked stimulation of cell proliferation, but there was no mitogenic effect of Pl-PLC on 3T3 fibroblasts. Studies with exogenously added 125I-bFGF revealed that about 6.5% and 20% of the cell surface-bound bFGF were released by treatment with Pl-PLC and heparitinase, respectively. Both enzymes also released sulfate-labeled heparan sulfate from metabolically labeled 3T3 fibroblasts. Pl-PLC failed to release 125I-bFGF from the subendothelial extracellular matrix (ECM), as compared to release of 60% of the ECM-bound bFGF by heparitinase. Our results indicate that 3-8% of the total cellular content of bFGF is associated with glycosyl-Pl anchored cell surface HSPG. This FGF may exert both autocrine and paracrine effects, provided that it is released by Pl-PLC and adequately presented to high affinity bFGF cell surface receptor sites.