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PMID: 2446619 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The cell surface hyaluronate binding sites of invasive human bladder carcinoma cells.

Biochemical and biophysical research communications ·Vol. 149 ·No. 1 ·1987-11-30 ·Pages 249-57

Nemec RE, Toole BP, Knudson W

Abstract

High-affinity, cell surface binding sites for hyaluronate were demonstrated on highly invasive human bladder carcinoma cells. These binding sites were shown to be specific for hyaluronate, saturable and exhibit a Km of 0.94 x 10(-9) M and a Bmax of 65 ng hyaluronate/10(6) cells. The binding of [3H]hyaluronate to a fixed cell-affinity column was competed with unlabeled hyaluronate and hyaluronate-hexasaccharide but not with hyaluronate-tetrasaccharide, chondroitin sulfate, heparin or non-sulfated dextran. Pre-treatment of cells with protease destroyed the binding activity whereas pretreatment with Streptomyces hyaluronidase to reveal occupied binding sites had no effect. No hyaluronate-binding activity was observed on normal human fibroblasts.

MeSH Terms
Binding, Competitive Carcinoma, Transitional Cell/metabolism Cell Membrane/metabolism Glycosaminoglycans/metabolism Humans Hyaluronan Receptors Hyaluronic Acid/metabolism Hyaluronoglucosaminidase/pharmacology Peptide Hydrolases/pharmacology Receptors, Cell Surface/metabolism Tumor Cells, Cultured Urinary Bladder Neoplasms/metabolism
Chemicals
Glycosaminoglycans Hyaluronan Receptors Receptors, Cell Surface Hyaluronic Acid Hyaluronoglucosaminidase Peptide Hydrolases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nemec R E
Department of Biochemistry, Rush-Presbyterian, St. Luke's Medical Center, Chicago, Il 60612.
Toole B P
Knudson W
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1987-11-30
Pages
249-57
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NCI NIH HHS · CA42614 · United States
NIDCR NIH HHS · DE05838 · United States
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