Stabilization by heparin of acidic fibroblast growth factor mitogenicity for human endothelial cells in vitro

The effects of heparin and other glycosaminoglycans (GAGs) on the mitogenicity and stability of acidic fibroblast growth factor (aFGF) were studied. The mitogenic activity of aFGF was assayed utilizing cultured adult human endothelial cells (AHECs) isolated from iliac arteries and veins as target cells. In most experiments, aFGF purified from bovine brain was employed; in some experiments recombinant bovine aFGF was used and qualitatively similar results were obtained. In the presence of heparin, bovine aFGF at doses between 0.5 and 1.0 ng/ml (30‐60 pM) elicited half the maximum AHEC growth over a 4‐day period depending on the cell line tested; in the absence of heparin, significant growth was not observed at aFGF concentrations less than 10‐20 ng/ml. This effect of heparin was dose‐dependent over the range 0.1‐10 μg/ml (half‐maximum dose, 2 μg/ml). The mitogenic activity of bovine aFGF for AHECs decreased by 50% after preincubation in culture medium without cells at 37°C for 2 ½ to 3 hours. In contrast, the mitogenic activity of bovine aFGF preincubated in the presence of heparin‐containing culture medium without cells was dramatically stabilized (half‐life 24‐29 hours). These effects also were observed in serum‐free medium. Several GAGs structurally related to heparin such as chondroitin‐4‐sulfate, chondroitin‐6‐sulfate, dermatan sulfate, and hyaluronic acid neither potentiated nor stabilized aFGF mitogenic activity. However, heparan sulfate from bovine lung was found to be nearly as active as heparin in both these effects. These data suggest that the binding and stabilization of mitogens by extracellular and tissue‐associated heparan sulfates might play important roles in the regulation of AHEC growth.