دورية أكاديمية

A dose-dependent response to MEK inhibition determines hypoblast fate in bovine embryos

التفاصيل البيبلوغرافية
العنوان: A dose-dependent response to MEK inhibition determines hypoblast fate in bovine embryos
المؤلفون: Canizo, Jesica R., Ynsaurralde Rivolta, Amada E., Vazquez Echegaray, Camila, Suvá, Mariana, Alberio, Virgilia, Aller, Juan F., Guberman, Alejandra Sonia, Salamone, Daniel Felipe, Alberio, Ricardo, Alberio, Ramiro
بيانات النشر: BioMed Central
المجموعة: CONICET Digital (Consejo Nacional de Investigaciones Científicas y Técnicas)
مصطلحات موضوعية: BOVINE EMBRYOS, EPIBLAST, HYPOBLAST, LIF, LINEAGE SEGREGATION, NANOG, PD0325901, SOX17, T2IGÖ, WNT INHIBITOR, https://purl.org/becyt/ford/4.4Test, https://purl.org/becyt/ford/4Test
الوصف: Background: The segregation of the hypoblast and the emergence of the pluripotent epiblast mark the final stages of blastocyst formation in mammalian embryos. In bovine embryos the formation of the hypoblast has been partially studied, and evidence shows that MEK signalling plays a limited role in the segregation of this lineage. Here we explored the role of different signalling pathways during lineage segregation in the bovine embryo using immunofluorescence analysis of NANOG and SOX17 as readouts of epiblast and hypoblast, respectively. Results: We show that SOX17 starts to be expressed in 16-32-cell stage embryos, whereas NANOG is first detected from 8-cell stage. SOX17 is first co-expressed with NANOG, but these markers become mutually exclusive by the late blastocyst stage. By assessing the expression kinetics of NANOG/SOX17 we show that inhibition of MEK signalling can eliminate SOX17 expression in bovine blastocysts, without altering NANOG expression. Modulation of WNT, PKC and LIF did not affect NANOG expression in the epiblast when used in combination with the ERK inhibitor. Conclusions: This study shows that SOX17 can be used as a reliable early marker of hypoblast in the bovine, and based on its expression profile we show that the hypoblast segregates in day 7 blastocysts. Furthermore, SOX17 expression is abolished using 1 μM of PD0325901, without affecting the NANOG population in the epiblast. Modulation of WNT, PKC and LIF are not sufficient to support enhanced NANOG expression in the epiblast when combined with ERK inhibitor, indicating that additional signalling pathways should be examined to determine their potential roles in epiblast expansion. ; Fil: Canizo, Jesica R. Universidad de Buenos Aires; Argentina. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Buenos Aires Sur. Estación Experimental Agropecuaria Balcarce. Agencia de Extensión Rural Balcarce; Argentina ; Fil: Ynsaurralde Rivolta, Amada E. Universidad de Buenos Aires; Argentina. Instituto Nacional de Tecnologia ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 1471-213X
العلاقة: info:eu-repo/semantics/altIdentifier/url/https://bmcdevbiol.biomedcentral.com/articles/10.1186/s12861-019-0193-9Test; http://hdl.handle.net/11336/123551Test; Canizo, Jesica R.; Ynsaurralde Rivolta, Amada E.; Vazquez Echegaray, Camila; Suvá, Mariana; Alberio, Virgilia; et al.; A dose-dependent response to MEK inhibition determines hypoblast fate in bovine embryos; BioMed Central; Bmc Developmental Biology; 19; 1; 7-2019; 1-13; CONICET Digital; CONICET
الإتاحة: https://doi.org/10.1186/s12861-019-0193-9Test
http://hdl.handle.net/11336/123551Test
حقوق: info:eu-repo/semantics/openAccess ; https://creativecommons.org/licenses/by-nc-sa/2.5/arTest/
رقم الانضمام: edsbas.695A7623
قاعدة البيانات: BASE