Abstract

Forces play diverse roles in vascular development, homeostasis and disease. VE-cadherin at endothelial cell-cell junctions links the contractile acto-myosin cytoskeletons of adjacent cells, serving as a tension-transducer. To explore tensile changes across VE-cadherin in live zebrafish, we tailored an optical biosensor approach, originally established in vitro. We validate localization and function of a VE-cadherin tension sensor (TS) in vivo. Changes in tension across VE-cadherin observed using ratio-metric or lifetime FRET measurements reflect acto-myosin contractility within endothelial cells. Furthermore, we apply the TS to reveal biologically relevant changes in VE-cadherin tension that occur as the dorsal aorta matures and upon genetic and chemical perturbations during embryonic development.

Details

Title
Live imaging molecular changes in junctional tension upon VE-cadherin in zebrafish
Author
Lagendijk, Anne Karine 1   VIAFID ORCID Logo  ; Gomez, Guillermo A 2   VIAFID ORCID Logo  ; Baek, Sungmin 1   VIAFID ORCID Logo  ; Hesselson, Daniel 3   VIAFID ORCID Logo  ; Hughes, William E 3 ; Paterson, Scott 1 ; Conway, Daniel E 4   VIAFID ORCID Logo  ; Heinz-Georg Belting 5   VIAFID ORCID Logo  ; Affolter, Markus 5   VIAFID ORCID Logo  ; Smith, Kelly A 1   VIAFID ORCID Logo  ; Schwartz, Martin A 6   VIAFID ORCID Logo  ; Yap, Alpha S 7   VIAFID ORCID Logo  ; Hogan, Benjamin M 1   VIAFID ORCID Logo 

 Institute for Molecular Bioscience, Genomics of Development and Disease division, The University of Queensland, St Lucia, QLD, Australia 
 Institute for Molecular Bioscience, Cell Biology and Molecular Medicine division, The University of Queensland, St Lucia, QLD, Australia; Centre for Cancer Biology, SA Pathology and the University of South Australia, Adelaide, SA, Australia 
 Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia 
 Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, VA, USA 
 Biozentrum der Universität Basel, Basel, Switzerland 
 Yale Cardiovascular Research Center and Department of Internal Medicine, Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT, USA 
 Institute for Molecular Bioscience, Cell Biology and Molecular Medicine division, The University of Queensland, St Lucia, QLD, Australia 
Pages
1-12
Publication year
2017
Publication date
Nov 2017
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1962258938
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.