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Increased expression of 6-phosphofructo-2-kinase/fructose 2,6-bisphosphatase-3 is required for growth of mouse embryonic stem cells that are undergoing differentiation

dc.contributor.authorGüzel, Saime
dc.contributor.authorGürpınar, Yunus
dc.contributor.authorAltunok, Tuğba Hazal
dc.contributor.authorYalçın, Abdullah
dc.contributor.buuauthorGÜZEL, SAİME
dc.contributor.buuauthorAltunok, Tuğba Hazal
dc.contributor.buuauthorYALÇIN, ABDULLAH
dc.contributor.departmentBursa Uludağ Üniversitesi/Veteriner Fakültesi/Biyokimya Anabilim Dalı.
dc.contributor.orcid0000-0001-8519-8375
dc.contributor.researcheridHEF-9447-2022
dc.contributor.researcheridGCY-0775-2022
dc.contributor.researcheridABI-4164-2020
dc.date.accessioned2024-09-09T08:21:29Z
dc.date.available2024-09-09T08:21:29Z
dc.date.issued2022-11-10
dc.description.abstractThe unlimited proliferation capacity of embryonic stem cells (ESCs) coupled with their capability to differentiate into several cell types makes them an attractive candidate for studying the molecular mechanisms regulating self-renewal and transition from pluripotent state. Although the roles of 6-phosphofructo-2-kinase/fructose-2,6-bisphos-phatase family (PFKFB1-4) in cell survival, proliferation, and differentiation in tumor cells have been studied, their role in mouse ESC (mESC) biology is currently unkown. In the current study, Pfkfb isoenzyme expressions were analyzed in R1 and J1 mESCs that were cultured in the presence and absence of leukemia inhibitory factor (LIF). We report that expression of the Pfkfb3 isoenzyme was markedly increased when mESCs were promoted to differentiate upon LIF removal. We then demonstrated that Pfkfb3 silencing induced the differentiation marker Brachyury suggesting that Pfkfb3 may be required for the regulation of mesodermal differentiation of mESCs. Furthermore, we show that the increase in Pfkfb3 expression is required for the growth of early differentiated mESCs. Although these results provide important insights into the early differentiation of mESCs with regard to Pfkfb expressions, further mechanistic studies will be needed for understanding the pathways and mechanisms involved in regulation of proliferation and early differentiation of mESCs through Pfkfb3.
dc.identifier.doi10.1007/s10616-022-00557-9
dc.identifier.endpage38
dc.identifier.issn0920-9069
dc.identifier.issue1
dc.identifier.startpage27
dc.identifier.urihttps://doi.org/10.1007/s10616-022-00557-9
dc.identifier.urihttps://link.springer.com/article/10.1007/s10616-022-00557-9
dc.identifier.urihttps://hdl.handle.net/11452/44395
dc.identifier.volume75
dc.identifier.wos000880554400001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherSpringer
dc.relation.bapOUAP(V)-2013/27
dc.relation.journalCytotechnology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.relation.tubitak116Z570
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPfkfb3
dc.subjectProliferation
dc.subjectPluripotency
dc.subjectGlycolysis
dc.subjectPathways
dc.subjectLif
dc.subjectMouse embryonic stem cells
dc.subject6-phosphofructo-2-kinase/fructose 2,6-bisphosphatase-3
dc.subjectBrachyury
dc.subjectLeukemia inhibitory factor
dc.subjectBiotechnology & applied microbiology
dc.subjectCell biology
dc.titleIncreased expression of 6-phosphofructo-2-kinase/fructose 2,6-bisphosphatase-3 is required for growth of mouse embryonic stem cells that are undergoing differentiation
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublication2efc12f6-c590-4fc1-9443-b8567ab92236
relation.isAuthorOfPublication24332407-6513-4c39-92c2-21a376f853b1
relation.isAuthorOfPublication.latestForDiscovery2efc12f6-c590-4fc1-9443-b8567ab92236

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