Abstract |
Glycation has been implicated in the endothelial dysfunction that contributes to both diabetes- and aging-associated vascular complications. The aim of the present study was to determine whether Amadori-glycated phosphatidylethanolamine ( Amadori-PE), a lipid-linked glycation compound that is formed at an increased rate in hyperglycemic states, affected proliferation, migration and tube formation of cultured human umbilical vein endothelial cells (HUVEC). Amadori-PE at a low concentration of less than 5 microM significantly enhanced these three factors involved in angiogenesis. Furthermore, stimulation of HUVEC with Amadori-PE resulted in secretion of matrix metalloproteinase 2 (MMP-2), a pivotal enzyme in the initial step of angiogenesis. Our results demonstrated for the first time that Amadori-PE may be an important compound that promotes vascular disease as a result of its angiogenic activity on endothelial cells. We also demonstrated that MMP-2 is a primary mediator of Amadori-PE-driven angiogenesis.
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Authors | Jeong-Ho Oak, Kiyotaka Nakagawa, Shinichi Oikawa, Teruo Miyazawa |
Journal | FEBS letters
(FEBS Lett)
Vol. 555
Issue 2
Pg. 419-23
(Dec 04 2003)
ISSN: 0014-5793 [Print] England |
PMID | 14644453
(Publication Type: Journal Article)
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Chemical References |
- Phosphatidylethanolamines
- Vascular Endothelial Growth Factors
- Collagenases
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Topics |
- Cell Division
(drug effects)
- Cell Movement
(drug effects)
- Cells, Cultured
- Collagenases
(metabolism)
- Endothelium, Vascular
(cytology, drug effects, metabolism)
- Fibroblasts
(drug effects, metabolism)
- Glycosylation
- Humans
- Neovascularization, Pathologic
(drug therapy)
- Phosphatidylethanolamines
(chemistry, pharmacology)
- Umbilical Veins
(cytology)
- Vascular Endothelial Growth Factors
(metabolism)
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