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Class 3 semaphorins in cardiovascular development

Secreted class 3 semaphorins (Sema3), which signal through holoreceptor complexes that are formed by different subunits, such as neuropilins (Nrps), proteoglycans, and plexins, were initially characterized as fundamental regulators of axon guidance during embryogenesis. Subsequently, Sema3A, Sema3C,...

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Detalles Bibliográficos
Autores principales: Valdembri, Donatella, Regano, Donatella, Maione, Federica, Giraudo, Enrico, Serini, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5160038/
https://www.ncbi.nlm.nih.gov/pubmed/27439112
http://dx.doi.org/10.1080/19336918.2016.1212805
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author Valdembri, Donatella
Regano, Donatella
Maione, Federica
Giraudo, Enrico
Serini, Guido
author_facet Valdembri, Donatella
Regano, Donatella
Maione, Federica
Giraudo, Enrico
Serini, Guido
author_sort Valdembri, Donatella
collection PubMed
description Secreted class 3 semaphorins (Sema3), which signal through holoreceptor complexes that are formed by different subunits, such as neuropilins (Nrps), proteoglycans, and plexins, were initially characterized as fundamental regulators of axon guidance during embryogenesis. Subsequently, Sema3A, Sema3C, Sema3D, and Sema3E were discovered to play crucial roles in cardiovascular development, mainly acting through Nrp1 and Plexin D1, which funnels the signal of multiple Sema3 in vascular endothelial cells. Mechanistically, Sema3 proteins control cardiovascular patterning through the enzymatic GTPase-activating-protein activity of the cytodomain of Plexin D1, which negatively regulates the function of Rap1, a small GTPase that is well-known for its ability to drive vascular morphogenesis and to elicit the conformational activation of integrin adhesion receptors.
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spelling pubmed-51600382017-02-13 Class 3 semaphorins in cardiovascular development Valdembri, Donatella Regano, Donatella Maione, Federica Giraudo, Enrico Serini, Guido Cell Adh Migr Review Secreted class 3 semaphorins (Sema3), which signal through holoreceptor complexes that are formed by different subunits, such as neuropilins (Nrps), proteoglycans, and plexins, were initially characterized as fundamental regulators of axon guidance during embryogenesis. Subsequently, Sema3A, Sema3C, Sema3D, and Sema3E were discovered to play crucial roles in cardiovascular development, mainly acting through Nrp1 and Plexin D1, which funnels the signal of multiple Sema3 in vascular endothelial cells. Mechanistically, Sema3 proteins control cardiovascular patterning through the enzymatic GTPase-activating-protein activity of the cytodomain of Plexin D1, which negatively regulates the function of Rap1, a small GTPase that is well-known for its ability to drive vascular morphogenesis and to elicit the conformational activation of integrin adhesion receptors. Taylor & Francis 2016-07-20 /pmc/articles/PMC5160038/ /pubmed/27439112 http://dx.doi.org/10.1080/19336918.2016.1212805 Text en © 2016 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Review
Valdembri, Donatella
Regano, Donatella
Maione, Federica
Giraudo, Enrico
Serini, Guido
Class 3 semaphorins in cardiovascular development
title Class 3 semaphorins in cardiovascular development
title_full Class 3 semaphorins in cardiovascular development
title_fullStr Class 3 semaphorins in cardiovascular development
title_full_unstemmed Class 3 semaphorins in cardiovascular development
title_short Class 3 semaphorins in cardiovascular development
title_sort class 3 semaphorins in cardiovascular development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5160038/
https://www.ncbi.nlm.nih.gov/pubmed/27439112
http://dx.doi.org/10.1080/19336918.2016.1212805
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