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Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis

AIMS: The formation of cell–cell and cell–extra cellular matrix (ECM) contacts by endothelial cells (ECs) is crucial for the stability and integrity of a vascular network. We previously identified cingulin-like 1 (Cgnl1) in a transcriptomic screen for new angiogenic modulators. Here we aim to study...

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Autores principales: Chrifi, Ihsan, Hermkens, Dorien, Brandt, Maarten M, van Dijk, Christian G M, Bürgisser, Petra E, Haasdijk, Remco, Pei, Jiayi, van de Kamp, Esther H M, Zhu, Changbin, Blonden, Lau, Kros, Johan M, Duncker, Dirk J, Duckers, Henricus J, Cheng, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852532/
https://www.ncbi.nlm.nih.gov/pubmed/29016873
http://dx.doi.org/10.1093/cvr/cvx175
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author Chrifi, Ihsan
Hermkens, Dorien
Brandt, Maarten M
van Dijk, Christian G M
Bürgisser, Petra E
Haasdijk, Remco
Pei, Jiayi
van de Kamp, Esther H M
Zhu, Changbin
Blonden, Lau
Kros, Johan M
Duncker, Dirk J
Duckers, Henricus J
Cheng, Caroline
author_facet Chrifi, Ihsan
Hermkens, Dorien
Brandt, Maarten M
van Dijk, Christian G M
Bürgisser, Petra E
Haasdijk, Remco
Pei, Jiayi
van de Kamp, Esther H M
Zhu, Changbin
Blonden, Lau
Kros, Johan M
Duncker, Dirk J
Duckers, Henricus J
Cheng, Caroline
author_sort Chrifi, Ihsan
collection PubMed
description AIMS: The formation of cell–cell and cell–extra cellular matrix (ECM) contacts by endothelial cells (ECs) is crucial for the stability and integrity of a vascular network. We previously identified cingulin-like 1 (Cgnl1) in a transcriptomic screen for new angiogenic modulators. Here we aim to study the function of the cell–cell junction associated protein Cgnl1 during vessel formation. METHODS AND RESULTS: Unlike family member cingulin, Cgnl1 expression is enriched in ECs during vascular growth. Cgnl1 is important for the formation of multicellular tubule structures, as shown in vitro using loss-of function assays in a 3D matrix co-culture system that uses primary human ECs and supporting mural cells. Further studies revealed that Cgnl1 regulates vascular growth by promoting Ve-cadherin association with the actin cytoskeleton, thereby stabilizing adherens junctions. Cgnl1 also regulates focal adhesion assembly in response to ECM contact, promoting vinculin and paxillin recruitment and focal adhesion kinase signalling. In vivo, we demonstrate in a postnatal retinal vascular development model in mice that Cgnl1 function is crucial for sustaining neovascular growth and stability. CONCLUSIONS: Our data demonstrate a functional relevance for Cgnl1 as a defining factor in new vessel formation both in vitro and in vivo.
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spelling pubmed-58525322018-03-23 Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis Chrifi, Ihsan Hermkens, Dorien Brandt, Maarten M van Dijk, Christian G M Bürgisser, Petra E Haasdijk, Remco Pei, Jiayi van de Kamp, Esther H M Zhu, Changbin Blonden, Lau Kros, Johan M Duncker, Dirk J Duckers, Henricus J Cheng, Caroline Cardiovasc Res Original Articles AIMS: The formation of cell–cell and cell–extra cellular matrix (ECM) contacts by endothelial cells (ECs) is crucial for the stability and integrity of a vascular network. We previously identified cingulin-like 1 (Cgnl1) in a transcriptomic screen for new angiogenic modulators. Here we aim to study the function of the cell–cell junction associated protein Cgnl1 during vessel formation. METHODS AND RESULTS: Unlike family member cingulin, Cgnl1 expression is enriched in ECs during vascular growth. Cgnl1 is important for the formation of multicellular tubule structures, as shown in vitro using loss-of function assays in a 3D matrix co-culture system that uses primary human ECs and supporting mural cells. Further studies revealed that Cgnl1 regulates vascular growth by promoting Ve-cadherin association with the actin cytoskeleton, thereby stabilizing adherens junctions. Cgnl1 also regulates focal adhesion assembly in response to ECM contact, promoting vinculin and paxillin recruitment and focal adhesion kinase signalling. In vivo, we demonstrate in a postnatal retinal vascular development model in mice that Cgnl1 function is crucial for sustaining neovascular growth and stability. CONCLUSIONS: Our data demonstrate a functional relevance for Cgnl1 as a defining factor in new vessel formation both in vitro and in vivo. Oxford University Press 2017-12 2017-08-31 /pmc/articles/PMC5852532/ /pubmed/29016873 http://dx.doi.org/10.1093/cvr/cvx175 Text en © The Author 2017. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Chrifi, Ihsan
Hermkens, Dorien
Brandt, Maarten M
van Dijk, Christian G M
Bürgisser, Petra E
Haasdijk, Remco
Pei, Jiayi
van de Kamp, Esther H M
Zhu, Changbin
Blonden, Lau
Kros, Johan M
Duncker, Dirk J
Duckers, Henricus J
Cheng, Caroline
Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis
title Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis
title_full Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis
title_fullStr Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis
title_full_unstemmed Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis
title_short Cgnl1, an endothelial junction complex protein, regulates GTPase mediated angiogenesis
title_sort cgnl1, an endothelial junction complex protein, regulates gtpase mediated angiogenesis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852532/
https://www.ncbi.nlm.nih.gov/pubmed/29016873
http://dx.doi.org/10.1093/cvr/cvx175
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