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dc.contributor.authorArat, Sezen
dc.contributor.authorCaputcu, Arzu Tas
dc.contributor.authorÇevik, Mesut
dc.contributor.authorAkkoç, Tolga
dc.contributor.authorÇetinkaya, Gaye
dc.contributor.authorBagis, Haydar
dc.date.accessioned2022-05-11T14:45:24Z
dc.date.available2022-05-11T14:45:24Z
dc.date.issued2016
dc.identifier.issn0967-1994
dc.identifier.issn1469-8730
dc.identifier.urihttps://doi.org/10.1017/S0967199415000519
dc.identifier.urihttps://hdl.handle.net/20.500.11776/10034
dc.description.abstractThis study was conducted to determine the additive effects of exogenous growth factors during in vitro oocyte maturation (IVM) and the sequential culture of nuclear transfer (NT) embryos. Oocyte maturation and culture of reconstructed embryos derived from bovine granulosa cells were performed in culture medium supplemented with either epidermal growth factor (EGF) alone or a combination of EGF with insulin-like growth factor-I (IGF-I). The maturation rates of oocytes matured in the presence of EGF or the EGF + IGF-I combination were significantly higher than those of oocytes matured in the presence of only fetal calf serum (FCS) (P < 0.05). The developing NT embryos showed no significant differences in fusion, cleavage or blastocyst rates among the culture groups (P > 0.05). IGF-I alone or in combination with EGF in sequential embryo culture medium significantly increased the ratio of inner cell mass (ICM) to total blastocyst cells (P < 0.05). Our results showed that the addition of growth factors to IVM and sequential culture media of cloned bovine embryos increased the ICM without changing the total cell number. These unknown and uncontrolled effects of growth factors can alter the allocation of ICM and trophectoderm cells (TE) in NT embryos. A decrease in TE cell numbers could be a reason for developmental abnormalities in embryos in the cloning system.en_US
dc.description.sponsorshipTUBITAKTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [KAMAG-106G005]en_US
dc.description.sponsorshipWe wish to thanks Dr. O. Yavuz for statistical analysis, Sakir Sekmen, Gazi Turgut and Erman Ates for technical assistance. The manuscript has been edited by native speaker Dr. Anita L. Akkas, who has PhD degree in English Literature and MA degree in Linguistics Engineering and Science. This research was supported by TUBITAK with grant number KAMAG-106G005 and was conducted at TUBITAK-MRC, the Genetic Engineering and Biotechnology Institute in Turkey.en_US
dc.language.isoengen_US
dc.publisherCambridge Univ Pressen_US
dc.identifier.doi10.1017/S0967199415000519
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBovineen_US
dc.subjectCell allocationen_US
dc.subjectCloningen_US
dc.subjectEmbryo cultureen_US
dc.subjectGrowth factorsen_US
dc.subjectIn-Vitro Fertilizationen_US
dc.subjectCulture-Mediumen_US
dc.subjectDevelopmental Competenceen_US
dc.subjectBlastocyst Developmenten_US
dc.subjectInsulinen_US
dc.subjectSupplementationen_US
dc.subjectOptimizationen_US
dc.subjectApoptosisen_US
dc.subjectReceptoren_US
dc.subjectPorcineen_US
dc.titleEffect of growth factors on oocyte maturation and allocations of inner cell mass and trophectoderm cells of cloned bovine embryosen_US
dc.typearticleen_US
dc.relation.ispartofZygoteen_US
dc.departmentFakülteler, Ziraat Fakültesi, Tarımsal Biyoteknoloji Bölümüen_US
dc.authorid0000-0002-1140-8058
dc.authorid0000-0002-2789-0635
dc.authorid0000-0003-2991-6322
dc.authorid0000-0002-0754-6116
dc.identifier.volume24en_US
dc.identifier.issue4en_US
dc.identifier.startpage554en_US
dc.identifier.endpage562en_US
dc.institutionauthorArat, Sezen
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid6603553213
dc.authorscopusid53463162500
dc.authorscopusid23396214300
dc.authorscopusid23767133200
dc.authorscopusid16400954400
dc.authorscopusid55919600100
dc.authorwosidBAĞIŞ/V-3827-2017
dc.authorwosidarat, sezen/ABA-7370-2020
dc.authorwosidÇEVİK, MESUT/AAI-2153-2020
dc.identifier.wosWOS:000378857100010en_US
dc.identifier.scopus2-s2.0-84943770600en_US
dc.identifier.pmid26444069en_US


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