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Diabetes, Vol 46, Issue 1 87-93, Copyright © 1997 by American Diabetes Association
Effect of extracellular matrix glycation on endothelial cell adhesion and spreading: involvement of vitronectin
IW Bobbink, HC de Boer, WL Tekelenburg, JD Banga and PG de Groot
Department of Haematology, University Hospital, Utrecht, The Netherlands.
Glycation of proteins of the vessel wall is thought to play an important
role in the pathogenesis of vascular complications in diabetes by affecting
structure and function of these proteins. Adhesive proteins in the
extracellular matrix (ECM) of endothelial cells (ECs) are essential for
attachment of ECs to the subintima. In this study, we investigated the
effect of glycation of ECM and purified adhesive proteins on EC adhesion
and spreading. ECM was incubated with the reactive sugar
glucose-6-phosphate (0-500 mmol/l) for different time periods (0-14 days)
at 37 degrees C. Degree of glycation, measured in an enzyme-linked
immunosorbent assay using a monoclonal antibody specific for advanced
glycation end products, increased in a time- and concentration-dependent
manner. Glycation of ECM with 50 mmol/l glucose-6-phosphate resulted in
increased coverage by ECs as measured in a cell adhesion assay and was the
result of an increase in number of adhered cells, while cell size was
unaffected. Glycation of ECM with higher concentrations of
glucose-6-phosphate resulted in decreased coverage by ECs caused by both a
reduction in number of adhered ECs and impaired spreading. Experiments with
purified glycated matrix proteins indicate that the decrease in EC adhesion
and spreading on glycated ECM may result from glycation of vitronectin.
Impaired EC adhesion and spreading caused by vitronectin glycation may
result in impaired endothelial function and contribute to vascular disease.

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Copyright © 1997 by the American Diabetes Association.
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