The impact of high density receptor clusters on VEGF signaling
Vascular endothelial growth factor (VEGF) signaling is involved in the process of blood vessel development and maintenance. Signaling is initiated by binding of the bivalent VEGF ligand to the membrane-bound receptors (VEGFR), which in turn stimulates receptor dimerization. Herein, we discuss experi...
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2013-08-01
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Series: | Electronic Proceedings in Theoretical Computer Science |
Online Access: | http://arxiv.org/pdf/1309.0868v1 |
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doaj-b18188ec889140398ad073ff4b087e372020-11-24T22:05:53ZengOpen Publishing AssociationElectronic Proceedings in Theoretical Computer Science2075-21802013-08-01125Proc. HSB 2013375210.4204/EPTCS.125.3The impact of high density receptor clusters on VEGF signalingYe ChenChristopher ShortÁdám M. HalászJeremy S. EdwardsVascular endothelial growth factor (VEGF) signaling is involved in the process of blood vessel development and maintenance. Signaling is initiated by binding of the bivalent VEGF ligand to the membrane-bound receptors (VEGFR), which in turn stimulates receptor dimerization. Herein, we discuss experimental evidence that VEGF receptors localize in caveloae and other regions of the plasma membrane, and for other receptors, it has been shown that receptor clustering has an impact on dimerization and thus also on signaling. Overall, receptor clustering is part of a complex ecosystem of interactions and how receptor clustering impacts dimerization is not well understood. To address these questions, we have formulated the simplest possible model. We have postulated the existence of a single high affinity region in the cell membrane, which acts as a transient trap for receptors. We have defined an ODE model by introducing high- and low-density receptor variables and introduce the corresponding reactions from a realistic model of VEGF signal initiation. Finally, we use the model to investigate the relation between the degree of VEGFR concentration, ligand availability, and signaling. In conclusion, our simulation results provide a deeper understanding of the role of receptor clustering in cell signaling.http://arxiv.org/pdf/1309.0868v1 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ye Chen Christopher Short Ádám M. Halász Jeremy S. Edwards |
spellingShingle |
Ye Chen Christopher Short Ádám M. Halász Jeremy S. Edwards The impact of high density receptor clusters on VEGF signaling Electronic Proceedings in Theoretical Computer Science |
author_facet |
Ye Chen Christopher Short Ádám M. Halász Jeremy S. Edwards |
author_sort |
Ye Chen |
title |
The impact of high density receptor clusters on VEGF signaling |
title_short |
The impact of high density receptor clusters on VEGF signaling |
title_full |
The impact of high density receptor clusters on VEGF signaling |
title_fullStr |
The impact of high density receptor clusters on VEGF signaling |
title_full_unstemmed |
The impact of high density receptor clusters on VEGF signaling |
title_sort |
impact of high density receptor clusters on vegf signaling |
publisher |
Open Publishing Association |
series |
Electronic Proceedings in Theoretical Computer Science |
issn |
2075-2180 |
publishDate |
2013-08-01 |
description |
Vascular endothelial growth factor (VEGF) signaling is involved in the process of blood vessel development and maintenance. Signaling is initiated by binding of the bivalent VEGF ligand to the membrane-bound receptors (VEGFR), which in turn stimulates receptor dimerization. Herein, we discuss experimental evidence that VEGF receptors localize in caveloae and other regions of the plasma membrane, and for other receptors, it has been shown that receptor clustering has an impact on dimerization and thus also on signaling. Overall, receptor clustering is part of a complex ecosystem of interactions and how receptor clustering impacts dimerization is not well understood. To address these questions, we have formulated the simplest possible model. We have postulated the existence of a single high affinity region in the cell membrane, which acts as a transient trap for receptors. We have defined an ODE model by introducing high- and low-density receptor variables and introduce the corresponding reactions from a realistic model of VEGF signal initiation. Finally, we use the model to investigate the relation between the degree of VEGFR concentration, ligand availability, and signaling. In conclusion, our simulation results provide a deeper understanding of the role of receptor clustering in cell signaling. |
url |
http://arxiv.org/pdf/1309.0868v1 |
work_keys_str_mv |
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