Source:http://linkedlifedata.com/resource/pubmed/id/11397702
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2001-6-8
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pubmed:abstractText |
Cultured arterial smooth muscle cells (SMCs) with distinct phenotypic features have been described by several laboratories; however, it is not presently known whether this phenotypic heterogeneity can be maintained within an in vivo environment. To answer this question, we have seeded into the intima of denuded rat carotid artery 2 SMC populations with well-established distinct biological features, ie, spindle-shaped, not growing in the absence of serum, and well differentiated versus epithelioid, growing in the absence of serum, and relatively undifferentiated, derived from the aortic media of newborn rats (aged 4 days) and old rats (aged >18 months), respectively. We show that these 2 populations maintain their distinct biochemical features (ie, expression of alpha-smooth muscle actin, smooth muscle myosin heavy chains, and cellular retinol binding protein-1) in the in vivo environment. The old rat media-derived SMCs continue to produce cellular retinol binding protein-1 but little alpha-smooth muscle actin and smooth muscle myosin heavy chains, whereas the newborn rat media-derived SMCs continue to express alpha-smooth muscle actin and smooth muscle myosin heavy chains but no cellular retinol binding protein-1. Our results reinforce the notion of arterial SMC phenotypic heterogeneity and suggest that in our model, heterogeneity is controlled genetically and not by the local environment.
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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/Actins,
http://linkedlifedata.com/resource/pubmed/chemical/Myosin Heavy Chains,
http://linkedlifedata.com/resource/pubmed/chemical/Rbp1 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Retinol-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Retinol-Binding Proteins, Cellular
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1524-4636
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
949-54
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11397702-Actins,
pubmed-meshheading:11397702-Animals,
pubmed-meshheading:11397702-Animals, Newborn,
pubmed-meshheading:11397702-Arteries,
pubmed-meshheading:11397702-Arteriosclerosis,
pubmed-meshheading:11397702-Carotid Artery Injuries,
pubmed-meshheading:11397702-Cells, Cultured,
pubmed-meshheading:11397702-Male,
pubmed-meshheading:11397702-Muscle, Smooth, Vascular,
pubmed-meshheading:11397702-Myosin Heavy Chains,
pubmed-meshheading:11397702-Phenotype,
pubmed-meshheading:11397702-Rats,
pubmed-meshheading:11397702-Rats, Inbred F344,
pubmed-meshheading:11397702-Retinol-Binding Proteins,
pubmed-meshheading:11397702-Retinol-Binding Proteins, Cellular
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pubmed:year |
2001
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pubmed:articleTitle |
Cultured arterial smooth muscle cells maintain distinct phenotypes when implanted into carotid artery.
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pubmed:affiliation |
Department of Pathology, University of Geneva, Geneva, Switzerland.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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