In this study an attempt was made to correlate the in-vitro anti-proliferative effect of heparin with the heparin binding on the cell surface. Cells with different sensitivities to the anti-proliferative effect of heparin (BHK-21, FAO, SMC, BAEC, A-431, V-79, and skin fibroblasts) were incubated with [H-3]heparin either in the presence or in the absence of unlabelled heparin. A saturable binding was found only in BHK-21, FAG, SMC, BAEC and V-79. Scatchard analysis revealed the presence of a single class of binding sites. The binding of [H-3]heparin was efficiently displaced by unlabelled heparin, pentosan polysulfate and low-molecular-weight heparin, but not by dermatan sulfate. Although the sensitivity to the anti-proliferative effect of heparin varied considerably among the cell types (BHK-21 >SMC, FAO >BAEC >V-79), there was no correlation between the reduction of proliferation of these cells and either their heparin binding capacity or the number of binding sites per cell.
Effect of heparin on cell proliferation: Lack of correlation with heparin binding sites on cell membrane / Tiozzo, Roberta; D., Reggiani; Ma, Croce; CALANDRA BUONAURA, Sebastiano; B., Osima; P., Bianchini. - In: DRUGS UNDER EXPERIMENTAL AND CLINICAL RESEARCH. - ISSN 0378-6501. - 23:(1997), pp. 103-109.
Effect of heparin on cell proliferation: Lack of correlation with heparin binding sites on cell membrane
TIOZZO, Roberta;CALANDRA BUONAURA, Sebastiano;
1997
Abstract
In this study an attempt was made to correlate the in-vitro anti-proliferative effect of heparin with the heparin binding on the cell surface. Cells with different sensitivities to the anti-proliferative effect of heparin (BHK-21, FAO, SMC, BAEC, A-431, V-79, and skin fibroblasts) were incubated with [H-3]heparin either in the presence or in the absence of unlabelled heparin. A saturable binding was found only in BHK-21, FAG, SMC, BAEC and V-79. Scatchard analysis revealed the presence of a single class of binding sites. The binding of [H-3]heparin was efficiently displaced by unlabelled heparin, pentosan polysulfate and low-molecular-weight heparin, but not by dermatan sulfate. Although the sensitivity to the anti-proliferative effect of heparin varied considerably among the cell types (BHK-21 >SMC, FAO >BAEC >V-79), there was no correlation between the reduction of proliferation of these cells and either their heparin binding capacity or the number of binding sites per cell.Pubblicazioni consigliate
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