Source:http://linkedlifedata.com/resource/pubmed/id/16462802
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-2-7
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pubmed:abstractText |
The angiopoietins Ang-1 and Ang-2 have been identified as ligands of the receptor tyrosine kinase Tie-2 (refs. 1,2). Paracrine Ang-1-mediated activation of Tie-2 acts as a regulator of vessel maturation and vascular quiescence. In turn, the antagonistic ligand Ang-2 acts by an autocrine mechanism and is stored in endothelial Weibel-Palade bodies from where it can be rapidly released upon stimulation. The rapid release of Ang-2 implies functions of the angiopoietin-Tie system beyond its established role during vascular morphogenesis as a regulator of rapid vascular responses. Here we show that mice deficient in Ang-2 (encoded by the gene Angpt2) cannot elicit an inflammatory response in thioglycollate-induced or Staphylococcus aureus-induced peritonitis, or in the dorsal skinfold chamber model. Recombinant Ang-2 restores the inflammation defect in Angpt2(-/-) mice. Intravital microscopy showed normal TNF-alpha-induced leukocyte rolling in the vasculature of Angpt2(-/-)mice, but rolling cells did not firmly adhere to activated endothelium. Cellular experiments showed that Ang-2 promotes adhesion by sensitizing endothelial cells toward TNF-alpha and modulating TNF-alpha-induced expression of endothelial cell adhesion molecules. Together, these findings identify Ang-2 as an autocrine regulator of endothelial cell inflammatory responses. Ang-2 thereby acts as a switch of vascular responsiveness exerting a permissive role for the activities of proinflammatory cytokines.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Angiopoietin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Angiopoietin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Inflammation Mediators,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1078-8956
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pubmed:author |
pubmed-author:AugustinHellmut GHG,
pubmed-author:FiedlerUlrikeU,
pubmed-author:GaleNicholas WNW,
pubmed-author:GrunowVerenaV,
pubmed-author:HerrmannMatthiasM,
pubmed-author:KoidlStefanieS,
pubmed-author:PreissnerKlaus TKT,
pubmed-author:ReissYvonneY,
pubmed-author:RosseauSimoneS,
pubmed-author:ScharpfeneckerMarionM,
pubmed-author:SobkeAstridA,
pubmed-author:SuttorpNorbertN,
pubmed-author:ThurstonGavinG,
pubmed-author:VajkoczyPeterP,
pubmed-author:WitzenrathMartinM
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pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
235-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16462802-Angiopoietin-1,
pubmed-meshheading:16462802-Angiopoietin-2,
pubmed-meshheading:16462802-Animals,
pubmed-meshheading:16462802-Cytokines,
pubmed-meshheading:16462802-Endothelium, Vascular,
pubmed-meshheading:16462802-Humans,
pubmed-meshheading:16462802-Inflammation,
pubmed-meshheading:16462802-Inflammation Mediators,
pubmed-meshheading:16462802-Mice,
pubmed-meshheading:16462802-Mice, Knockout,
pubmed-meshheading:16462802-Models, Biological,
pubmed-meshheading:16462802-Neovascularization, Pathologic,
pubmed-meshheading:16462802-Signal Transduction,
pubmed-meshheading:16462802-Tumor Necrosis Factor-alpha
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pubmed:year |
2006
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pubmed:articleTitle |
Angiopoietin-2 sensitizes endothelial cells to TNF-alpha and has a crucial role in the induction of inflammation.
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pubmed:affiliation |
Department of Vascular Biology and Angiogenesis Research, Tumor Biology Center, Freiburg 79106, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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