Source:http://linkedlifedata.com/resource/pubmed/id/17101841
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2006-12-22
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pubmed:abstractText |
Prolyl hydroxylase domain 2 protein (PHD2) signals the degradation of hypoxia-inducible factor (HIF)-1alpha by hydroxylating specific prolyl residues located within oxygen-dependent degradation domains. As expected, endothelial cells (ECs) overexpressing PHD2 had reduced HIF-1alpha and vascular endothelial growth factor-A expression and failed to accelerate their proliferation in response to hypoxia. Surprisingly, although these cells displayed further reductions in HIF-1alpha and vascular endothelial growth factor-A expression when cultured under normoxia, there was no further reduction in EC proliferation. Thus, there seemed to be no consistent correlation between PHD2 hydroxylase-mediated suppression of HIF-1alpha expression and inhibition of EC growth. Indeed, overexpression of a mutant PHD2 lacking hydroxylase activity also greatly diminished EC response to hypoxia-induced increase in proliferation, in spite of the fact that hypoxia-induced HIF-1alpha accumulation was not affected by mutant PHD2. These data strongly suggest the existence of a hydroxylase-independent mechanism for PHD2-mediated inhibition of EC proliferation under hypoxia. In support of a physiological relevance of PHD2 overexpression, we found that endogenous PHD2 expression was significantly upregulated by hypoxia and that silencing of the Phd2 gene by RNA interference significantly enhanced hypoxia-induced EC proliferation. In conclusion, this study demonstrates that PHD2 may act as a negative feedback regulator to antagonize hypoxia-induced EC proliferation.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Egln1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Hypoxia-Inducible Factor 1, alpha...,
http://linkedlifedata.com/resource/pubmed/chemical/Immediate-Early Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Procollagen-Proline Dioxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor A,
http://linkedlifedata.com/resource/pubmed/chemical/vascular endothelial growth factor...
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1524-4563
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
178-84
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17101841-Anoxia,
pubmed-meshheading:17101841-Cell Line,
pubmed-meshheading:17101841-Cell Proliferation,
pubmed-meshheading:17101841-DNA-Binding Proteins,
pubmed-meshheading:17101841-Endothelial Cells,
pubmed-meshheading:17101841-Feedback, Physiological,
pubmed-meshheading:17101841-Gene Silencing,
pubmed-meshheading:17101841-Hydroxylation,
pubmed-meshheading:17101841-Hypoxia-Inducible Factor 1, alpha Subunit,
pubmed-meshheading:17101841-Immediate-Early Proteins,
pubmed-meshheading:17101841-Mutation,
pubmed-meshheading:17101841-Procollagen-Proline Dioxygenase,
pubmed-meshheading:17101841-Transfection,
pubmed-meshheading:17101841-Up-Regulation,
pubmed-meshheading:17101841-Vascular Endothelial Growth Factor A
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pubmed:year |
2007
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pubmed:articleTitle |
Prolyl hydroxylase domain 2 protein suppresses hypoxia-induced endothelial cell proliferation.
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pubmed:affiliation |
Center for Vascular Biology, University of Connecticut Health Center, 263 Farmington Ave, Farmington, CT 06030-3501, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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