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Flow-induced HDAC1 phosphorylation and nuclear export in angiogenic sprouting.


ABSTRACT: Angiogenesis requires the coordinated growth and migration of endothelial cells (ECs), with each EC residing in the vessel wall integrating local signals to determine whether to remain quiescent or undergo morphogenesis. These signals include vascular endothelial growth factor (VEGF) and flow-induced mechanical stimuli such as interstitial flow, which are both elevated in the tumor microenvironment. However, it is not clear how VEGF signaling and mechanobiological activation due to interstitial flow cooperate during angiogenesis. Here, we show that endothelial morphogenesis is histone deacetylase-1- (HDAC1) dependent and that interstitial flow increases the phosphorylation of HDAC1, its activity, and its export from the nucleus. Furthermore, we show that HDAC1 inhibition decreases endothelial morphogenesis and matrix metalloproteinase-14 (MMP14) expression. Our results suggest that HDAC1 modulates angiogenesis in response to flow, providing a new target for modulating vascularization in the clinic.

SUBMITTER: Bazou D 

PROVIDER: S-EPMC5037418 | biostudies-literature | 2016 Sep

REPOSITORIES: biostudies-literature

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Flow-induced HDAC1 phosphorylation and nuclear export in angiogenic sprouting.

Bazou Despina D   Ng Mei Rosa MR   Song Jonathan W JW   Chin Shan Min SM   Maimon Nir N   Munn Lance L LL  

Scientific reports 20160927


Angiogenesis requires the coordinated growth and migration of endothelial cells (ECs), with each EC residing in the vessel wall integrating local signals to determine whether to remain quiescent or undergo morphogenesis. These signals include vascular endothelial growth factor (VEGF) and flow-induced mechanical stimuli such as interstitial flow, which are both elevated in the tumor microenvironment. However, it is not clear how VEGF signaling and mechanobiological activation due to interstitial  ...[more]

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