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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1998-8-17
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pubmed:databankReference | |
pubmed:abstractText |
Lysophosphatidylcholine (lysoPC), a component of oxidatively modified lipoproteins, is present in atherosclerotic lesions, and its proatherogenic properties have been demonstrated. To gain an insight into lysoPC-mediated endothelial gene expression, we applied nonradioactive differential display analysis of mRNA from lysoPC-treated and untreated human umbilical vein endothelial cells. We identified 12 up-regulated distinct genes including 5 cell growth-related genes (two phosphatases CL100 and B23/hVH-3, gravin, activating transcription factor-4, and heparin-binding epidermal growth factor-like growth factor), 3 thrombosis-related genes (plasminogen activator inhibitor-1, tissue plasminogen activator, and thrombomodulin), and 4 others (stanniocalcin, NAD-dependent methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase, BENE, and reducing agents and tunicamycin-responsive protein). We isolated a full-length cDNA of human gravin. The cDNA sequence of gravin was homologous with rat mitogenic regulatory gene or rat protein kinase C binding protein and substrate, suggesting that gravin would regulate cell growth. Thus, lysoPC apparently accelerates atherosclerosis by regulating the expression of a wide variety of genes. Our data suggest the involvement in atherogenesis of the genes hitherto regarded as atherosclerosis-unrelated.
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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/A Kinase Anchor Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/AKAP12 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Akap12 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Lysophosphatidylcholines,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0021-924X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
123
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1119-26
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pubmed:dateRevised |
2007-12-19
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pubmed:meshHeading |
pubmed-meshheading:9604001-A Kinase Anchor Proteins,
pubmed-meshheading:9604001-Amino Acid Sequence,
pubmed-meshheading:9604001-Animals,
pubmed-meshheading:9604001-Base Sequence,
pubmed-meshheading:9604001-Cell Cycle Proteins,
pubmed-meshheading:9604001-Cell Division,
pubmed-meshheading:9604001-Cells, Cultured,
pubmed-meshheading:9604001-DNA, Complementary,
pubmed-meshheading:9604001-Endothelium, Vascular,
pubmed-meshheading:9604001-Gene Expression Regulation,
pubmed-meshheading:9604001-Humans,
pubmed-meshheading:9604001-Lysophosphatidylcholines,
pubmed-meshheading:9604001-Molecular Sequence Data,
pubmed-meshheading:9604001-Protein Biosynthesis,
pubmed-meshheading:9604001-Proteins,
pubmed-meshheading:9604001-Rats,
pubmed-meshheading:9604001-Thrombosis
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pubmed:year |
1998
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pubmed:articleTitle |
Changes of gene expression by lysophosphatidylcholine in vascular endothelial cells: 12 up-regulated distinct genes including 5 cell growth-related, 3 thrombosis-related, and 4 others.
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pubmed:affiliation |
National Cardiovascular Center Research Institute, Suita, Osaka, 565-8565, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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