Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
44
pubmed:dateCreated
2008-11-5
pubmed:abstractText
Urokinase-type plasminogen activator (uPA) is expressed at elevated levels in atherosclerotic human arteries, primarily in macrophages. Plasminogen (Plg), the primary physiologic substrate of uPA, is present at significant levels in blood and interstitial fluid. Both uPA and Plg have activities that could affect atherosclerosis progression. Moreover, correlations between increased Plg activation and accelerated atherosclerosis are reported in several human studies. However, a coherent picture of the role of the uPA/Plg system in atherogenesis has not yet emerged, with at least one animal study suggesting that Plg is atheroprotective. We used a transgenic mouse model of macrophage-targeted uPA overexpression in apolipoprotein E-deficient mice to investigate the roles of uPA and Plg in atherosclerosis. We found that macrophage-expressed uPA accelerated atherosclerotic plaque growth and promoted aortic root dilation through Plg-dependent pathways. These pathways appeared to affect lesion progression rather than initiation and to include actions that disproportionately increase lipid accumulation in the artery wall. In addition, loss of Plg was protective against atherosclerosis both in the presence and absence of uPA overexpression. Transgenic mice with macrophage-targeted uPA overexpression reveal atherogenic roles for both uPA and Plg and are a useful experimental setting for investigating the molecular mechanisms that underlie clinically established relationships between uPA expression, Plg activation, and atherosclerosis progression.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-10073948, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-10073949, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-10213688, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-11304480, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-12461559, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-12690199, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-1334458, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-15095009, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-15096455, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-15205586, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-15261889, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-15345515, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-16554301, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-17379840, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-17431190, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-17681345, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-18037995, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-1829461, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-6605349, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-7670959, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-8987777, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-9005988, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-9294211, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-9398846, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-9490683, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-9531045, http://linkedlifedata.com/resource/pubmed/commentcorrection/18957535-9819364
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1091-6490
pubmed:author
pubmed:issnType
Electronic
pubmed:day
4
pubmed:volume
105
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
17109-14
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
Plasminogen mediates the atherogenic effects of macrophage-expressed urokinase and accelerates atherosclerosis in apoE-knockout mice.
pubmed:affiliation
Department of Medicine, University of Washington, 1959 Northeast Pacific Street, Seattle, WA 98195, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural