hymecromone and sodium-sulfate

hymecromone has been researched along with sodium-sulfate* in 1 studies

Other Studies

1 other study(ies) available for hymecromone and sodium-sulfate

ArticleYear
Inhibition of endothelial cell morphogenetic interactions in vitro by alpha- and beta-xylosides.
    In vitro cellular & developmental biology : journal of the Tissue Culture Association, 1988, Volume: 24, Issue:7

    Bovine aortic endothelial cells retain the ability to undergo histiotypic morphogenetic interactions in vitro as evidenced by a) the reversible expression of a sprouting cell phenotype and b) the patterned self-association of these sprouting cells into three-dimensional meshworks and tubule-like structures. These morphogenetic events are inhibited by xylosides in a dose-dependent manner. Two types of beta-xylosides (p-nitrophenyl-beta-D-xylopyranoside and 4-methylumbelliferyl-beta-D-xylopyranoside) and one alpha-xyloside (p-nitrophenyl-alpha-D-xylopyranoside) were tested. beta-xylosides are well characterized acceptors of glycosaminoglycan chains, whereas alpha-xylosides do not function in this capacity and have been extensively used as negative controls when studying the effects of beta-xylosides. Both alpha- and beta-xylosides inhibited endothelial morphogenetic interactions. This inhibition was slowly reversed during the 6- to 7-d period following removal of the xyloside. Inhibition of morphogenetic interactions by xylosides occurred at concentrations (0.5 to 2.0 mM) that had no demonstrable effects on cell proliferation, migration, or adhesion to 2-D plastic or collagen substrata. The xylosides seemed to inhibit cell spreading on a 3-D environment, they also inhibited the incorporation of [3H]-proline and Na2 35SO4 into the extracellular matrix deposited by the cells, suggesting that the inhibition of morphogenesis may be related to the inhibition of matrix deposition. Endothelial morphogenetic interactions were not inhibited by the extracellular matrix or by the conditioned medium produced by cells cultured in the presence of xylosides.

    Topics: Animals; Aorta; Cattle; Cell Adhesion; Cell Division; Cell Movement; Cells, Cultured; Culture Media; Endothelium, Vascular; Extracellular Matrix; Glycosides; Hymecromone; Morphogenesis; Phenotype; Proline; Sulfates

1988