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Stem cell factor/c-Kit signaling in in vitro cultures supports early mouse embryonic development by accelerating proliferation via a mechanism involving Akt-downstream genes

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dc.contributor.authorLim, Jung Jin-
dc.contributor.authorEum, Jin Hee-
dc.contributor.authorLee, Jeoung Eun-
dc.contributor.authorKim, Eun Sun-
dc.contributor.authorChung, Hyung Min-
dc.contributor.authorYoon, Tae Ki-
dc.contributor.authorKim, Kye-Seong-
dc.contributor.authorLee, Dong Ryul-
dc.date.accessioned2022-12-20T11:08:13Z-
dc.date.available2022-12-20T11:08:13Z-
dc.date.issued2010-11-
dc.identifier.issn1058-0468-
dc.identifier.issn1573-7330-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/173506-
dc.description.abstractStem cell factor (SCF)/c-Kit regulates the proliferation and survival of germ cells or stem cells; however, little is known about the role of SCF/c-Kit in pre-implantation embryo development. Using exogenous SCF supplementation and c-Kit siRNA injection, we investigated the role and mechanism of SCF/c-Kit in pre-implantation mouse embryos. Addition of soluble SCF to the culture medium improved blastocyst formation. c-Kit gene silencing reduced the rate of blastocyst formation and delayed embryonic development. The number of proliferating cells in c-Kit gene-silenced blastocysts decreased, whereas the number of apoptotic cells in blastocysts obtained from both experimental and the control groups was not affected. RT-PCR, immunostaining and western blotting revealed that proliferation-related Akt downstream targets were substantially affected by c-Kit gene silencing. SCF/c-Kit signaling through Akt downstream targets is likely involved in mediating the cleavage and proliferation of blastomeres during mouse pre-implantation embryogenesis.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherKluwer Academic/Plenum Publishers-
dc.titleStem cell factor/c-Kit signaling in in vitro cultures supports early mouse embryonic development by accelerating proliferation via a mechanism involving Akt-downstream genes-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1007/s10815-010-9449-9-
dc.identifier.scopusid2-s2.0-78651310256-
dc.identifier.wosid000284550600006-
dc.identifier.bibliographicCitationJournal of Assisted Reproduction and Genetics, v.27, no.11, pp 619 - 627-
dc.citation.titleJournal of Assisted Reproduction and Genetics-
dc.citation.volume27-
dc.citation.number11-
dc.citation.startPage619-
dc.citation.endPage627-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalResearchAreaObstetrics & Gynecology-
dc.relation.journalResearchAreaReproductive Biology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryObstetrics & Gynecology-
dc.relation.journalWebOfScienceCategoryReproductive Biology-
dc.subject.keywordPlusC-KIT-
dc.subject.keywordPlusPREIMPLANTATION DEVELOPMENT-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusKINASE-
dc.subject.keywordPlusLIGAND-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusRNA-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordAuthorStem cell factor (SCF)-
dc.subject.keywordAuthorc-Kit receptor-
dc.subject.keywordAuthorEmbryonic cleavage-
dc.subject.keywordAuthorGene silencing-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s10815-010-9449-9-
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