Dual Action of Sulfated Hyaluronan on Angiogenic Processes in Relation to Vascular Endothelial Growth Factor-A

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Linda Koehler
Gloria Ruiz-Gómez
Kanagasabai Balamurugan
Sandra Rother
Joanna Freyse
Stephanie Möller
Matthias Schnabelrauch
Sebastian Köhling
Snezana Djordjevic
Dieter Scharnweber
Jörg Rademann
M. Teresa Pisabarro
Vera Hintze
机构
[1] Max Bergmann Center of Biomaterials,Institute of Materials Science
[2] TU Dresden,Structural Bioinformatics
[3] BIOTEC TU Dresden,Institute of Pharmacy
[4] Freie Universität Berlin,Biomaterials Department
[5] INNOVENT e.V.,Institute of Structural and Molecular Biology
[6] University College London,Department of Cellular and Molecular Medicine, Glycobiology Research and Training Center
[7] University of California,undefined
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Pathological healing characterized by abnormal angiogenesis presents a serious burden to patients’ quality of life requiring innovative treatment strategies. Glycosaminoglycans (GAG) are important regulators of angiogenic processes. This experimental and computational study revealed how sulfated GAG derivatives (sGAG) influence the interplay of vascular endothelial growth factor (VEGF)165 and its heparin-binding domain (HBD) with the signaling receptor VEGFR-2 up to atomic detail. There was profound evidence for a HBD-GAG-HBD stacking configuration. Here, the sGAG act as a “molecular glue” leading to recognition modes in which sGAG interact with two VEGF165-HBDs. A 3D angiogenesis model demonstrated the dual regulatory role of high-sulfated derivatives on the biological activity of endothelial cells. While GAG alone promote sprouting, they downregulate VEGF165-mediated signaling and, thereby, elicit VEGF165-independent and -dependent effects. These findings provide novel insights into the modulatory potential of sGAG derivatives on angiogenic processes and point towards their prospective application in treating abnormal angiogenesis.
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