Author(s):
Jin, Yi ; Ding, Yindi ; Richards, Mark ; Kaakinen, Mika ; Giese, Wolfgang ; Baumann, Elisabeth ; Szymborska, Anna ; Rosa, André ; Nordling, Sofia ; Schimmel, Lilian ; Akmeriç, Emir Bora ; Pena, Andreia ; Nwadozi, Emmanuel ; Jamalpour, Maria ; Holstein, Katrin ; Sáinz-Jaspeado, Miguel ; Bernabeu, Miguel O. ; Welsh, Michael ; Gordon, Emma ; Franco, Claudio A. ; Vestweber, Dietmar ; Eklund, Lauri ; Gerhardt, Holger ; Claesson-Welsh, Lena
Date: 2022
Persistent ID: http://hdl.handle.net/10400.14/42831
Origin: Veritati - Repositório Institucional da Universidade Católica Portuguesa
Description
Vascular endothelial (VE)-cadherin in endothelial adherens junctions is an essential component of the vascular barrier, critical for tissue homeostasis and implicated in diseases such as cancer and retinopathies. Inhibitors of Src cytoplasmic tyrosine kinase have been applied to suppress VE-cadherin tyrosine phosphorylation and prevent excessive leakage, edema and high interstitial pressure. Here we show that the Src-related Yes tyrosine kinase, rather than Src, is localized at endothelial cell (EC) junctions where it becomes activated in a flow-dependent manner. EC-specific Yes1 deletion suppresses VE-cadherin phosphorylation and arrests VE-cadherin at EC junctions. This is accompanied by loss of EC collective migration and exaggerated agonist-induced macromolecular leakage. Overexpression of Yes1 causes ectopic VE-cadherin phosphorylation, while vascular leakage is unaffected. In contrast, in EC-specific Src deficiency, VE-cadherin internalization is maintained and leakage is suppressed. In conclusion, Yes-mediated phosphorylation regulates constitutive VE-cadherin turnover, thereby maintaining endothelial junction plasticity and vascular integrity.
