Abstract
Low molecular mass dermatan sulfate, obtained by depolymerization, induced the entrance in S phase of mitosis, enhanced the activity of matrix metalloproteinase-2, and could modulate cell migration of endothelial cells, through mechanisms independent of TNF-α autocrine regulation. LMMDS located at the injured sites could influence early stages of angiogenesis.
Copyright © 2012. Published by Elsevier Ltd.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cell Movement / drug effects
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Cell Proliferation / drug effects
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Cells, Cultured
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Dermatan Sulfate / pharmacology*
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Endothelial Cells / cytology
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Endothelial Cells / drug effects*
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Endothelial Cells / metabolism
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Matrix Metalloproteinase 2 / genetics
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Matrix Metalloproteinase 2 / metabolism*
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Mice
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Molecular Weight
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Myocardium / cytology
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S Phase / drug effects
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Tumor Necrosis Factor-alpha / biosynthesis
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Tumor Necrosis Factor-alpha / metabolism
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Up-Regulation
Substances
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Tumor Necrosis Factor-alpha
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Dermatan Sulfate
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Matrix Metalloproteinase 2