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Sökning: onr:"swepub:oai:lup.lub.lu.se:57ab1777-5964-4091-a9ab-cbd9fd159f1a" > Oxidized LDL and ly...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004095naa a2200409 4500
001oai:lup.lub.lu.se:57ab1777-5964-4091-a9ab-cbd9fd159f1a
003SwePub
008160404s1999 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:1930511
024a https://lup.lub.lu.se/record/12966652 URI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:19305112 URI
024a https://doi.org/10.1161/01.atv.19.12.30252 DOI
040 a (SwePub)lud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Dichtl, Wolfgang4 aut
2451 0a Oxidized LDL and lysophosphatidylcholine stimulate plasminogen activator inhibitor-1 expression in vascular smooth muscle cells
264 1b Ovid Technologies (Wolters Kluwer Health),c 1999
520 a Plasminogen activator inhibitor-1 (PAI-1) functions as an important regulator of fibrinolysis by inhibiting both tissue-type and urokinase-type plasminogen activator. PAI-1 is produced by smooth muscle cells (SMCs) in atherosclerotic arteries, but the mechanisms responsible for induction of PAI-1 in SMCs are less well understood. In cultured human aortic SMCs, PAI-1 mRNA expression and protein secretion were increased after incubation with oxidized low-density lipoprotein (LDL) and the lipid peroxidation product lysophosphatidylcholine, whereas the effects of native LDL on PAI-1 production and release were more variable and did not reach statistical significance. The effect of LDL on arterial expression of PAI-1 in vivo was also studied in an animal model. Intravenous injection of human LDL in Sprague-Dawley rats resulted in accumulation of apolipoprotein B in the aorta within 12 hours as assessed by immunohistochemical testing. Epitopes specific for oxidized LDL began to develop in the aorta 12 hours after injection of LDL and peaked at 24 hours; this peak was accompanied by intense expression of PAI-1 immunoreactivity in the media. Also, increased aortic expression of PAI-1 mRNA after LDL injection was detected by using in situ hybridization. The transcription factor activator protein-1, which is known to bind to the promoter of the PAI-1 gene, was activated in the aortic wall 24 hours after LDL injection as assessed by electrophoretic mobility shift assay. Pretreatment of LDL with the antioxidant probucol decreased expression of oxidized LDL and PAI-1 immunoreactivity and activator protein-1 induction in the aorta but did not affect expression of apolipoprotein B immunoreactivity. These findings demonstrate that LDL oxidation enhances secretion of PAI-1 from cultured SMCs and that a similar mechanism may be involved in vascular expression of PAI-1.
700a Stiko, Ann4 aut
700a Eriksson, Peru Karolinska Institutet4 aut
700a Goncalves, Isabelu Lund University,Lunds universitet,Kardiovaskulär forskning - immunitet och ateroskleros,Forskargrupper vid Lunds universitet,Kardiovaskulär forskning - translationella studier,Cardiovascular Research - Immunity and Atherosclerosis,Lund University Research Groups,Cardiovascular Research - Translational Studies4 aut0 (Swepub:lu)medf-igo
700a Calara, Frederico4 aut
700a Banfi, Cristina4 aut
700a Ares, Mikko P4 aut
700a Hamsten, Andersu Karolinska Institutet4 aut
700a Nilsson, Jan4 aut
710a Karolinska Institutetb Kardiovaskulär forskning - immunitet och ateroskleros4 org
773t Arteriosclerosis, Thrombosis, and Vascular Biologyd : Ovid Technologies (Wolters Kluwer Health)g 19:12, s. 32-3025q 19:12<32-3025x 1079-5642x 1524-4636
856u http://atvb.ahajournals.org/content/19/12/3025.longy FULLTEXT
856u http://www.ncbi.nlm.nih.gov/pubmed/10591684x freey FULLTEXT
856u https://www.ahajournals.org/doi/pdf/10.1161/01.ATV.19.12.3025
8564 8u https://lup.lub.lu.se/record/1296665
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:1930511
8564 8u https://doi.org/10.1161/01.atv.19.12.3025

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