Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/1904
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dc.contributor.authorSamad, Ghadir AbdelLatif Elen_US
dc.contributor.authorBazzi, Sameren_US
dc.contributor.authorKaram, Marcen_US
dc.contributor.authorBoudjeltia, Karim Zouaouien_US
dc.contributor.authorVanhamme, Lucen_US
dc.contributor.authorDaher, Jalilen_US
dc.date.accessioned2020-12-23T09:02:38Z-
dc.date.available2020-12-23T09:02:38Z-
dc.date.issued2019-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/1904-
dc.description.abstractCardiovascular disease associated with atherosclerosis is a leading cause of death worldwide. Atherosclerosis is primarily caused by the dysfunction of vascular endothelial cells and the subendothelial accumulation of oxidized forms of low‑density lipoproteins (LDL). Early observations have associated fibrin deposition with atheroma plaque formation, which has led to the proposition that a decrease in endothelial cell fibrinolysis may negatively influence atherogenesis. It has been recently demonstrated that myeloperoxidase modified LDL (MoxLDL) decreases endothelial cell profibrinolytic capacity in real‑time. The present study investigated the role of MoxLDL in endothelial cell dysfunction by determining the molecules that may be involved in decreasing the fibrinolysis of human aortic endothelial cells (HAEC). Accordingly, reverse transcription‑quantitative PCR was performed to screen for the differential expression of major genes that are implicated in the fibrinolytic process. In addition, the response of the latter cell type to MoxLDL was compared with bovine aortic endothelial (BAE) cells. Furthermore, the effect of the treatment on the generation of reactive oxygen species (ROS) was also determined. Although the current study did not demonstrate an association between MoxLDL treatment and a change in the expression of any major fibrinolytic factor in HAEC, a discrepancy between HAEC and BAE cells with respect to their response to modified LDL treatment was observed. The result have also demonstrated that MoxLDL does not increase ROS generation in HAEC as opposed to the other major type of modified LDL, cupper oxidized LDL (CuoxLDL) that was reported to exhibit a positive effect at this level. The present study provided important insight into the different effects of MoxLDL and CuoxLDL in endothelial cells, which may aid future studies to determine the various signaling pathways that are promoted by these molecules. The results of the present study may be utili.en_US
dc.language.isoengen_US
dc.subjectMyeloperoxidase oxidized low-densityen_US
dc.subjectFibrinolysisen_US
dc.subjectEndothelial cellsen_US
dc.subjectHuman aortic endothelialen_US
dc.subjectBovine aortic endothelial cellsen_US
dc.subject.lcshAtherosclerosisen_US
dc.titleEffect of myeloperoxidase modified LDL on bovine and human aortic endothelial cellsen_US
dc.typeJournal Articleen_US
dc.contributor.affiliationDepartment of Biologyen_US
dc.contributor.affiliationDepartment of Biologyen_US
dc.contributor.affiliationDepartment of Biologyen_US
dc.description.volume18en_US
dc.description.issue6en_US
dc.description.startpage4567en_US
dc.description.endpage4574en_US
dc.date.catalogued2020-06-15-
dc.description.statusPublisheden_US
dc.identifier.OlibID253125-
dc.identifier.openURLhttps://www.spandidos-publications.com/10.3892/etm.2019.8109#en_US
dc.relation.ispartoftextExperimental and therapeutic medicine journalen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Biology
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