PROTEOGLYCAN SYNTHESIS BY NORMAL AND NEOPLASTIC HUMAN TRANSITIONAL EPITHELIAL-CELLS

Metabolically 35S‐labeled proteoglycans were isolated from cell‐associated matrices and media of confluent cultures of human normal transitional epithelial cells and HCV‐29T transitional carcinoma cells. On Sepharose CL‐4B columns, the cell‐associated proteoglycans synthesized from both cell types separated into three identical size classes, termed Cl, Cll, and Clll. Normal epithelial cell C‐fractions eluted in a 22:34:45 proportion and contained 64%, 64%, and 72% heparan sulfate, whereas corresponding HCV‐29T fractions eluted in a 29:11:60 proportion, and contained 91%, 77%, and 70% heparan sulfate, respectively. Medium proteoglycans from normal cells separated into two size classes in a proportion of 6:94 and were composed of 35% and 50% heparan sulfate. HCV‐29T medium contained only one size class of proteoglycans consisting of 23% heparan sulfate. The remaining percent‐ages were accounted for by chondroitin/dermatan sulfate. On isopycnic CsCI gradients, proteoglycan fractions from normal cells had buoyant densities that were higher than the corresponding fractions from HCV‐29T cells. DEAE‐Sephacel chromatography showed that cell and medium associated heparan sulfate from HCV‐29T cells was consistently of lower charge density (undersulfated) than that from normal epithelial cells. In contrast, the chondroitin/dermatan sulfate of HCV‐29T was of a charge density similar to that of normal cells. These as well as other structural and compositional differences in the proteoglycan may account, at least in part, for the altered behavioral traits of highly invasive carcinoma cells. Copyright © 1990 Wiley‐Liss, Inc.