Control of endothelial cell proliferation and migration by VEGF signaling to histone deacetylase 7.

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Citation

Wang S, Li X, Parra M, Verdin E, Bassel-Duby R, Olson EN

Control of endothelial cell proliferation and migration by VEGF signaling to histone deacetylase 7.

Proc Natl Acad Sci U S A. 2008 Jun 3;105(22):7738-43. doi: 10.1073/pnas.0802857105. Epub 2008 May 28.

PubMed ID
18509061 [ View in PubMed
]
Abstract

VEGF has been shown to regulate endothelial cell (EC) proliferation and migration. However, the nuclear mediators of the actions of VEGF in ECs have not been fully defined. We show that VEGF induces the phosphorylation of three conserved serine residues in histone deacetylase 7 (HDAC7) via protein kinase D, which promotes nuclear export of HDAC7 and activation of VEGF-responsive genes in ECs. Expression of a signal-resistant HDAC7 mutant protein in ECs inhibits proliferation and migration in response to VEGF. These results demonstrate that phosphorylation of HDAC7 serves as a molecular switch to mediate VEGF signaling and endothelial function.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Serine/threonine-protein kinase D1Q15139Details