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Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model

The angiopoietin-Tie signaling pathway is an important vascular signaling pathway involved in angiogenesis, vascular stability, and quiescence. Dysregulation in the pathway is linked to the impairments in vascular function associated with many diseases, including cancer, ocular diseases, systemic in...

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Detalles Bibliográficos
Autores principales: Zhang, Yu, Kontos, Christopher D., Annex, Brian H., Popel, Aleksander S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806670/
https://www.ncbi.nlm.nih.gov/pubmed/31655061
http://dx.doi.org/10.1016/j.isci.2019.10.006
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author Zhang, Yu
Kontos, Christopher D.
Annex, Brian H.
Popel, Aleksander S.
author_facet Zhang, Yu
Kontos, Christopher D.
Annex, Brian H.
Popel, Aleksander S.
author_sort Zhang, Yu
collection PubMed
description The angiopoietin-Tie signaling pathway is an important vascular signaling pathway involved in angiogenesis, vascular stability, and quiescence. Dysregulation in the pathway is linked to the impairments in vascular function associated with many diseases, including cancer, ocular diseases, systemic inflammation, and cardiovascular diseases. The present study uses a computational signaling pathway model validated against experimental data to quantitatively study various mechanistic aspects of the angiopoietin-Tie signaling pathway, including receptor activation, trafficking, turnover, and molecular mechanisms of its regulation. The model provides mechanistic insights into the controversial role of Ang2 and its regulators vascular endothelial protein tyrosine phosphatase (VE-PTP) and Tie1 and predicts synergistic effects of inhibition of VE-PTP, Tie1, and Tie2 cleavage on enhancing the vascular protective actions of Tie2.
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spelling pubmed-68066702019-10-28 Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model Zhang, Yu Kontos, Christopher D. Annex, Brian H. Popel, Aleksander S. iScience Article The angiopoietin-Tie signaling pathway is an important vascular signaling pathway involved in angiogenesis, vascular stability, and quiescence. Dysregulation in the pathway is linked to the impairments in vascular function associated with many diseases, including cancer, ocular diseases, systemic inflammation, and cardiovascular diseases. The present study uses a computational signaling pathway model validated against experimental data to quantitatively study various mechanistic aspects of the angiopoietin-Tie signaling pathway, including receptor activation, trafficking, turnover, and molecular mechanisms of its regulation. The model provides mechanistic insights into the controversial role of Ang2 and its regulators vascular endothelial protein tyrosine phosphatase (VE-PTP) and Tie1 and predicts synergistic effects of inhibition of VE-PTP, Tie1, and Tie2 cleavage on enhancing the vascular protective actions of Tie2. Elsevier 2019-10-03 /pmc/articles/PMC6806670/ /pubmed/31655061 http://dx.doi.org/10.1016/j.isci.2019.10.006 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Zhang, Yu
Kontos, Christopher D.
Annex, Brian H.
Popel, Aleksander S.
Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model
title Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model
title_full Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model
title_fullStr Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model
title_full_unstemmed Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model
title_short Angiopoietin-Tie Signaling Pathway in Endothelial Cells: A Computational Model
title_sort angiopoietin-tie signaling pathway in endothelial cells: a computational model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806670/
https://www.ncbi.nlm.nih.gov/pubmed/31655061
http://dx.doi.org/10.1016/j.isci.2019.10.006
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