نمایش مختصر رکورد

dc.contributor.authorMahdavinezhad, Foroughen_US
dc.contributor.authorKazemi, Parinazen_US
dc.contributor.authorFathalizadeh, Parisaen_US
dc.contributor.authorSarmadi, Fatemehen_US
dc.contributor.authorSotoodeh, Leilaen_US
dc.contributor.authorHashemi, Ehsanen_US
dc.contributor.authorHajarian, Hadien_US
dc.contributor.authorDashtizad, Mojtabaen_US
dc.date.accessioned1399-07-08T20:19:27Zfa_IR
dc.date.accessioned2020-09-29T20:19:27Z
dc.date.available1399-07-08T20:19:27Zfa_IR
dc.date.available2020-09-29T20:19:27Z
dc.date.issued2019-02-01en_US
dc.date.issued1397-11-12fa_IR
dc.date.submitted2018-01-10en_US
dc.date.submitted1396-10-20fa_IR
dc.identifier.citationMahdavinezhad, Forough, Kazemi, Parinaz, Fathalizadeh, Parisa, Sarmadi, Fatemeh, Sotoodeh, Leila, Hashemi, Ehsan, Hajarian, Hadi, Dashtizad, Mojtaba. (2019). In vitro versus In vivo: Development-, Apoptosis-, and Implantation-Related Gene Expression in Mouse Blastocyst. Iranian Journal of Biotechnology, 17(1), 90-97. doi: 10.21859/ijb.2157en_US
dc.identifier.issn1728-3043
dc.identifier.issn2322-2921
dc.identifier.urihttps://dx.doi.org/10.21859/ijb.2157
dc.identifier.urihttp://www.ijbiotech.com/article_75680.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/85856
dc.description.abstract<strong>Background:</strong> While mammalian embryos can adapt to their environments, their sensitivity overshadows their adaptability in suboptimal <em>in vitro</em> conditions. Therefore, the environment in which the gametes are fertilized or to which the embryo is exposed can greatly affect the quality of the embryo and consequently its implantation potential.<br /> <strong>Objectives:</strong> Since providing an optimal culture condition needs a deep understanding of the environmental effects, and regarding the fact that normal morphology fails to be a reliable indicator of natural embryo development, the current study aimed at comparing <em>in vivo</em>- and <em>in vitro</em>-derived blastocysts at the molecular level.<br /> <strong>Materials and Methods:</strong> <em>In vivo</em> and <em>in vitro</em> mouse blastocysts were obtained by flushing the uterine horns and <em>in vitro</em> fertilization/culture, respectively. Normal blastocysts of both groups were evaluated in terms of hatching rate and expression of three lineage-differentiation-, apoptosis-, and implantation-related genes.<br /> <strong>Results:</strong> The hatching rate was lower in <em>In vitro</em> fertilization (IVF)-produced blastocysts in comparison with that of the <em>in vivo </em>counterparts. More importantly, the study results indicated significant changes in the expression levels of eight out of ten selected genes, especially <em>Mmp-9</em> (about -10.7-fold). The expression of <em>Mmp-9 </em>in trophoblast cells is required for successful implantation and trophoblast invasion.<br /> <strong>Conclusions:</strong> The current study, in addition to confirming that the altered gene expression pattern of <em>in vitro</em>-produced embryos resulted in normal morphology, provided a possible reason for lower implantation rate of <em>in vitro</em>-produced blastocysts regarding the <em>Mmp-9</em> expression.en_US
dc.format.extent692
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherNational Institute of Genetic Engineering and Biotechnologyen_US
dc.relation.ispartofIranian Journal of Biotechnologyen_US
dc.relation.isversionofhttps://dx.doi.org/10.21859/ijb.2157
dc.subjectGene expressionen_US
dc.subjectfertilization in vitroen_US
dc.subjectMatrix Metalloproteinase 9en_US
dc.subjectMedical Biotechnologyen_US
dc.titleIn vitro versus In vivo: Development-, Apoptosis-, and Implantation-Related Gene Expression in Mouse Blastocysten_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.contributor.departmentEmbryo Biotechnology Laboratory (Embio Lab), Department of Animal Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iranen_US
dc.contributor.departmentEmbryo Biotechnology Laboratory (Embio Lab), Department of Animal Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iranen_US
dc.contributor.departmentEmbryo Biotechnology Laboratory (Embio Lab), Department of Animal Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iranen_US
dc.contributor.departmentEmbryo Biotechnology Laboratory (Embio Lab), Department of Animal Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB)en_US
dc.contributor.departmentEmbryo Biotechnology Laboratory (Embio Lab), Department of Animal Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iranen_US
dc.contributor.departmentEmbryo Biotechnology Laboratory (Embio Lab), Department of Animal Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iranen_US
dc.contributor.departmentDepartment of Animal Science, Razi University, Kermanshah, Iranen_US
dc.contributor.departmentEmbryo Biotechnology Laboratory (Embio Lab), Department of Animal Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iranen_US
dc.citation.volume17
dc.citation.issue1
dc.citation.spage90
dc.citation.epage97


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