نمایش مختصر رکورد

dc.contributor.authorOladnabi, Mortezaen_US
dc.contributor.authorBagheri, Abouzaren_US
dc.contributor.authorRezaei Kanavi, Mozhganen_US
dc.contributor.authorAzadmehr, Abbasen_US
dc.contributor.authorKianmehr, Anvarsadaten_US
dc.date.accessioned1399-07-09T08:21:16Zfa_IR
dc.date.accessioned2020-09-30T08:21:16Z
dc.date.available1399-07-09T08:21:16Zfa_IR
dc.date.available2020-09-30T08:21:16Z
dc.date.issued2019-02-01en_US
dc.date.issued1397-11-12fa_IR
dc.date.submitted2017-07-18en_US
dc.date.submitted1396-04-27fa_IR
dc.identifier.citationOladnabi, Morteza, Bagheri, Abouzar, Rezaei Kanavi, Mozhgan, Azadmehr, Abbas, Kianmehr, Anvarsadat. (2019). Extremely low frequency-pulsed electromagnetic fields affect proangiogenic-related gene expression in retinal pigment epithelial cells. Iranian Journal of Basic Medical Sciences, 22(2), 128-133. doi: 10.22038/ijbms.2018.25023.6214en_US
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.urihttps://dx.doi.org/10.22038/ijbms.2018.25023.6214
dc.identifier.urihttp://ijbms.mums.ac.ir/article_12011.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/339837
dc.description.abstract<em><strong>Objective(s):</strong></em> It is known that extremely low frequency-pulsed electromagnetic fields (ELF-PEMF) influence multiple cellular and molecular processes. Retinal pigment epithelial (RPE) cells have a significant part in the emergence and pathophysiology of several ocular disorders, such as neovascularization. This study assessed the impact of ELF-PEMF on the proangiogenic features of RPE cells. <br /><em><strong>Materials and Methods:</strong></em> Primary cultured RPE cells were treated with ELF-PEMF (50 Hz) for three days. Using ELISA assay, we evaluated the effects of treatment on RPE cell proliferation and apoptosis. Also, RT-PCR was used to determine the gene expression of proangiogenic factors, such as matrix metalloproteinase-2 (MMP-2), MMP-9, vascular endothelial growth factors receptor 2 (VEGFR-2), hypoxia-inducible factor 1 (HIF-1α), VEGFA, cathepsin D, connective tissue growth factor (CTGF), E2F3, tissue inhibitors of metalloproteinases 1 (TIMP-1), and TIMP-2.<br /><em><strong>Results:</strong></em> No noticeable changes were observed in cell proliferation and cell death of ELF-PEMF-exposed RPE cells, while transcript levels of proangiogenic genes (HIF-1α, VEGFA, VEGFR-2, CTGF, cathepsin D, TIMP-1, E2F3, MMP-2, and MMP-9) increased significantly.<br /><em><strong>Conclusion:</strong></em> RPE cells are important for homeostasis of the retina. ELF-PEMF increased the gene expression of proangiogenic factors in RPE cells, which highlights concerns about the impact of this treatment on human health.en_US
dc.format.extent537
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Basic Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijbms.2018.25023.6214
dc.subjectELF-PEMFen_US
dc.subjectGene expressionen_US
dc.subjectProangiogenic factorsen_US
dc.subjectQuantitative real-time PCRen_US
dc.subjectRPE cellsen_US
dc.subjectOtheren_US
dc.titleExtremely low frequency-pulsed electromagnetic fields affect proangiogenic-related gene expression in retinal pigment epithelial cellsen_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentStem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentDepartment of Clinical Biochemistry and Genetics, Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iranen_US
dc.contributor.departmentTissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iranen_US
dc.contributor.departmentImmunology Department, Babol University of Medical Sciences, Babol, Iranen_US
dc.contributor.departmentMedical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.citation.volume22
dc.citation.issue2
dc.citation.spage128
dc.citation.epage133
nlai.contributor.orcid0000-0001-7037-5084
nlai.contributor.orcid0000-0001-5604-1870


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