Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction

During the formation of the zebrafish dorsal longitudinal anastomotic vessel, blood vessels connect in a process called anastomosis. Using live imaging, the authors here show that endothelial cell movements during blood vessel anastomosis are associated with oscillating lamellipodia-like structures,...

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Autores principales:	Ilkka Paatero, Loïc Sauteur, Minkyoung Lee, Anne K. Lagendijk, Daniel Heutschi, Cora Wiesner, Camilo Guzmán, Dimitri Bieli, Benjamin M. Hogan, Markus Affolter, Heinz-Georg Belting
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2018
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/7819155b39d244c7a779701c32e360d4
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spelling	oai:doaj.org-article:7819155b39d244c7a779701c32e360d42021-12-02T15:33:58ZJunction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction10.1038/s41467-018-05851-92041-1723https://doaj.org/article/7819155b39d244c7a779701c32e360d42018-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-05851-9https://doaj.org/toc/2041-1723During the formation of the zebrafish dorsal longitudinal anastomotic vessel, blood vessels connect in a process called anastomosis. Using live imaging, the authors here show that endothelial cell movements during blood vessel anastomosis are associated with oscillating lamellipodia-like structures, oriented in the direction of the movements and emerging at endothelial cell junctions.Ilkka PaateroLoïc SauteurMinkyoung LeeAnne K. LagendijkDaniel HeutschiCora WiesnerCamilo GuzmánDimitri BieliBenjamin M. HoganMarkus AffolterHeinz-Georg BeltingNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-13 (2018)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Ilkka Paatero Loïc Sauteur Minkyoung Lee Anne K. Lagendijk Daniel Heutschi Cora Wiesner Camilo Guzmán Dimitri Bieli Benjamin M. Hogan Markus Affolter Heinz-Georg Belting Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction
description	During the formation of the zebrafish dorsal longitudinal anastomotic vessel, blood vessels connect in a process called anastomosis. Using live imaging, the authors here show that endothelial cell movements during blood vessel anastomosis are associated with oscillating lamellipodia-like structures, oriented in the direction of the movements and emerging at endothelial cell junctions.
format	article
author	Ilkka Paatero Loïc Sauteur Minkyoung Lee Anne K. Lagendijk Daniel Heutschi Cora Wiesner Camilo Guzmán Dimitri Bieli Benjamin M. Hogan Markus Affolter Heinz-Georg Belting
author_facet	Ilkka Paatero Loïc Sauteur Minkyoung Lee Anne K. Lagendijk Daniel Heutschi Cora Wiesner Camilo Guzmán Dimitri Bieli Benjamin M. Hogan Markus Affolter Heinz-Georg Belting
author_sort	Ilkka Paatero
title	Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction
title_short	Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction
title_full	Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction
title_fullStr	Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction
title_full_unstemmed	Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction
title_sort	junction-based lamellipodia drive endothelial cell rearrangements in vivo via a ve-cadherin-f-actin based oscillatory cell-cell interaction
publisher	Nature Portfolio
publishDate	2018
url	https://doaj.org/article/7819155b39d244c7a779701c32e360d4
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Junction-based lamellipodia drive endothelial cell rearrangements in vivo via a VE-cadherin-F-actin based oscillatory cell-cell interaction

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