Source:http://linkedlifedata.com/resource/pubmed/id/10764664
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
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| pubmed:dateCreated |
2000-4-27
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| pubmed:abstractText |
Smooth muscle cell (SMC) migration from the tunica media to the intima is a key event in the development of atherosclerotic lesions and in restenosis after angioplasty. SMCs require not only migratory but also degradative abilities that enable them to migrate through extracellular matrix proteins, which surround and embed these cells. We used a collagen type I lattice as a coating on top of a porous filter as a matrix barrier in a chamber to test the invasive behavior of SMCs in response to a chemoattractant (invasion assay) and compared that behavior with simple SMC migration through collagen type I-coated filters (migration assay). Inhibitors of matrix metalloproteinase, KB-R8301, tissue inhibitor of matrix metalloproteinase-1 (TIMP-1), TIMP-2, and peptide 74, attenuated platelet-derived growth factor-BB (PDGF-BB)-directed SMC invasion across the collagen lattice, whereas no effect was seen with these inhibitors on simple SMC migration through collagen-coated filters. RGD peptide inhibited SMC invasion but did not affect SMC migration. Anti-alphavbeta3 integrin antibody attenuated PDGF-BB-directed SMC invasion, whereas other antibodies against RGD-recognizing integrins, namely alphavbeta5 and alpha5, had no effect. None of these antibodies had any effect on simple SMC migration. RGD peptide and anti-alphavbeta3 antibody inhibited the attachment and spreading of SMCs on denatured collagen but not on native collagen. These findings indicate that there is a difference in the mechanisms between simple SMC migration across a collagen-coated filter and SMC invasion through a fibrillar collagen barrier. A proteolytic process is required for SMC invasion, and the degradation of matrix proteins alters the relationship between matrix protein molecules and SMC surface integrins.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Collagen,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxamic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/KB R8301,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinases,
http://linkedlifedata.com/resource/pubmed/chemical/Oligopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Platelet-Derived Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Vitronectin,
http://linkedlifedata.com/resource/pubmed/chemical/Tissue Inhibitor of...,
http://linkedlifedata.com/resource/pubmed/chemical/Tissue Inhibitor of...,
http://linkedlifedata.com/resource/pubmed/chemical/arginyl-glycyl-aspartic acid,
http://linkedlifedata.com/resource/pubmed/chemical/platelet-derived growth factor BB
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| pubmed:status |
MEDLINE
|
| pubmed:month |
Apr
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| pubmed:issn |
1079-5642
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
20
|
| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
998-1005
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:10764664-Animals,
pubmed-meshheading:10764664-Antibodies, Monoclonal,
pubmed-meshheading:10764664-Cattle,
pubmed-meshheading:10764664-Cell Adhesion,
pubmed-meshheading:10764664-Cell Movement,
pubmed-meshheading:10764664-Cells, Cultured,
pubmed-meshheading:10764664-Collagen,
pubmed-meshheading:10764664-Enzyme Inhibitors,
pubmed-meshheading:10764664-Hydroxamic Acids,
pubmed-meshheading:10764664-Kinetics,
pubmed-meshheading:10764664-Matrix Metalloproteinase 2,
pubmed-meshheading:10764664-Matrix Metalloproteinases,
pubmed-meshheading:10764664-Muscle, Smooth, Vascular,
pubmed-meshheading:10764664-Oligopeptides,
pubmed-meshheading:10764664-Platelet-Derived Growth Factor,
pubmed-meshheading:10764664-Protein Denaturation,
pubmed-meshheading:10764664-Receptors, Vitronectin,
pubmed-meshheading:10764664-Tissue Inhibitor of Metalloproteinase-1,
pubmed-meshheading:10764664-Tissue Inhibitor of Metalloproteinase-2
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| pubmed:year |
2000
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| pubmed:articleTitle |
Matrix metalloproteinase and alphavbeta3 integrin-dependent vascular smooth muscle cell invasion through a type I collagen lattice.
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| pubmed:affiliation |
Department of Geriatrics, Nagoya University Graduate School of Medicine, Nagoya. kanda3@spice.or.jp
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| pubmed:publicationType |
Journal Article
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