Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5181
DC FieldValueLanguage
dc.contributor.advisorDaher, Jalilen_US
dc.contributor.authorAzar, Elianaen_US
dc.date.accessioned2021-10-28T06:16:21Z-
dc.date.available2021-10-28T06:16:21Z-
dc.date.issued2021-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5181-
dc.descriptionIncludes bibliographical references (p. 40-47)en_US
dc.description.abstractBackground: Atherosclerosis is a chronic inflammatory disease that is characterized by a buildup of fat in the walls of arteries. Macrophages play a crucial role in the development of the disease by ingesting oxidized LDL particles and forming foam cells which are a hallmark of atherosclerosis. Oxidized low density lipoprotein (ox-LDL) is a major player in atherogenesis and many studies suggest that myeloperoxidase oxidized LDL (Mox-LDL) is an important patho-physiological model for LDL modification in vivo. While copper oxidized LDL (Cuox-LDL) is intensively studied in the context of atherosclerosis, little is known about the effects of Mox-LDL on monocyte and macrophage biology including their differentiation and polarization. Aim: Our study aimed at investigating Mox-LDL effects on macrophage polarization in vitro by comparing Mox-LDL to its Cuox-LDL counterpart and making use of the THP-1 cell line model. Methods: THP-1 monocytes were cultured and differentiated into M0 macrophages (MØs) by treatment with PMA in vitro. Then, resting macrophages were treated with both Mox-LDL and Cuox-LDL and then compared to M1 and M2 polarized macrophages. ELISA assays were performed to assess the levels of IL-6 and IL-10 cytokines in the culture supernatants under different conditions, while immunophenotyping was conducted by assessing the surface expression of CD80 and CD209 markers Results: CD80 expression was highly significant in M1-MØs when compared to all other subsets: M0-MØs, M2-MØs, and Mox-LDL treated M0-MØs. Similarly, CD209 was significantly expressed in M2-MØs when compared to the other subtypes. Although IL-6 release was minimal in all macrophages types except in the M1-MØs where it was upregulated as expected, the same M1-MØs subtype also showed a surprising and significant increase in IL-10 release. In our model, physiological concentrations of both Mox-LDL and Cuox-LDL had no significant effects on CD80/CD209 expression or IL-6/IL-10 release. Conclusion: In our model, we showed that Mox-LDL and Cuox-LDL treated M0-MØs did not exhibit any significant phenotypic changes in terms of CD surface expression or interleukins secretion. Our results suggest that both types of oxidized LDL are not able to stimulate M0-MØs towards an inflammatory nor an alternative phenotype. They also provide preliminary data that could help interpret better the role of Mox-LDL in macrophage differentiation in atherosclerosis.en_US
dc.description.statementofresponsibilityby Eliana Azaren_US
dc.format.extent1 online resource (xi, 47 pages) : ill., tablesen_US
dc.language.isoengen_US
dc.rightsThis object is protected by copyright, and is made available here for research and educational purposes. Permission to reuse, publish, or reproduce the object beyond the personal and educational use exceptions must be obtained from the copyright holderen_US
dc.subject.lcshAtherosclerosisen_US
dc.subject.lcshDissertations, Academicen_US
dc.subject.lcshUniversity of Balamand--Dissertationsen_US
dc.titleThe effect of cuox-LDL and MPO modified LDL on THP-1 macrophage polarization in vitroen_US
dc.typeThesisen_US
dc.contributor.corporateUniversity of Balamanden_US
dc.contributor.departmentDepartment of Biologyen_US
dc.contributor.facultyFaculty of Arts and Sciencesen_US
dc.contributor.institutionUniversity of Balamanden_US
dc.date.catalogued2021-10-28-
dc.description.degreeMSc in Biologyen_US
dc.description.statusUnpublisheden_US
dc.identifier.OlibID288524-
dc.rights.accessrightsThis item is under embargo until end of year 2023.en_US
dc.provenance.recordsourceOliben_US
Appears in Collections:UOB Theses and Projects
Show simple item record

Record view(s)

41
checked on Sep 22, 2022

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.