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May 12, 2015Nature Communications253 citationsOpen Access

Yes-associated protein regulates endothelial cell contact-mediated expression of angiopoietin-2

HCHyun-Jung ChoiHZHaiying ZhangHPHongryeol Park

Structured PICO

P
Population
Mouse retinal vessels and endothelial cells (in vitro and in vivo)
I
Intervention
Overexpression of YAP-active form, ANG-2 depletion, or soluble Tie-2 treatment
O
Outcome
Angiogenic sprouting, YAP subcellular localization, phosphorylation, and activitysurrogate

YAP acts as a critical regulator in angiogenesis by mediating VE-cadherin-dependent cell contacts and regulating ANG-2 expression.

Abstract

Angiogenesis is regulated by the dynamic interaction between endothelial cells (ECs). Hippo-Yes-associated protein (YAP) signalling has emerged as a key pathway that controls organ size and tissue growth by mediating cell contact inhibition. However, the role of YAP in EC has not been defined yet. Here, we show expression of YAP in the developing front of mouse retinal vessels. YAP subcellular localization, phosphorylation and activity are regulated by VE-cadherin-mediated-EC contacts. This VE-cadherin-dependent YAP phosphorylation requires phosphoinositide 3-kinase-Akt activation. We further identify angiopoietin-2 (ANG-2) as a potential transcriptional target of YAP in regulating angiogenic activity of EC in vitro and in vivo. Overexpression of YAP-active form in EC enhances angiogenic sprouting, and this effect is blocked by ANG-2 depletion or soluble Tie-2 treatment. These findings implicate YAP as a critical regulator in angiogenesis and provide new insights into the mechanism coordinating junctional stability and angiogenic activation of ECs.

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Cite This Study

Choi et al. (2015) studied this question.

synapsesocial.com/papers/69d576e462196bac97d9bd1chttps://doi.org/10.1038/ncomms7943
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