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Article: Regulation of human trophoblast surrogate Jeg-3 spheroids implantation potential by Wnt/β-catenin pathway and lin28a/let-7a axis

TitleRegulation of human trophoblast surrogate Jeg-3 spheroids implantation potential by Wnt/β-catenin pathway and lin28a/let-7a axis
Authors
KeywordsWnt/β-catenin signalling
Lin28a protein
mir-let-7a
Jeg-3 spheroids
Issue Date2020
PublisherAcademic Press. The Journal's web site is located at http://www.elsevier.com/locate/yexcr
Citation
Experimental Cell Research, 2020, v. 388 n. 1, p. article no. 111718 How to Cite?
AbstractSuccessful implantation happens only when the development of a competent blastocyst synchronized with the differentiation of a receptive uterus. The exact mechanism affecting embryo implantation competency is still unclear. Previous data from our laboratory showed that several members of the let-7 family were up-regulated in the implanting dormant blastocysts and prohibited embryo activation through down-regulation integrin-β3. However, how the mir-let-7 family is regulated is still a question. In this study, the in vitro co-culture model was applied to imitate implantation. Human embryo surrogate Jeg-3 spheroids and endometrium epithelial cells Ishikawa were used. The following views were demonstrated. Firstly,Wnt/β-catenin signaling is essential for Jeg-3 spheroids implantation. Secondly, mir-let-7a is repressed by Wnt signaling, and low let-7a is beneficial for spheroids attachment and outgrowth. Third, in contrast with let-7a, lin28a is up-regulated by Wnt and promotes attachment and outgrowth. Lastly, the function of Wnt in embryo surrogate spheroids in implantation is mediated through lin28a/let-7a axis. In summary, our findings suggest Wnt/β-catenin signaling strength human embryo surrogate spheroids implanting potential through regulation lin28a/let-7a axis.
Persistent Identifierhttp://hdl.handle.net/10722/293449
ISSN
2023 Impact Factor: 3.3
2023 SCImago Journal Rankings: 0.947
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLI, Q-
dc.contributor.authorChiu, PCN-
dc.contributor.authorYeung, WSB-
dc.contributor.authorLiu, W-
dc.date.accessioned2020-11-23T08:16:55Z-
dc.date.available2020-11-23T08:16:55Z-
dc.date.issued2020-
dc.identifier.citationExperimental Cell Research, 2020, v. 388 n. 1, p. article no. 111718-
dc.identifier.issn0014-4827-
dc.identifier.urihttp://hdl.handle.net/10722/293449-
dc.description.abstractSuccessful implantation happens only when the development of a competent blastocyst synchronized with the differentiation of a receptive uterus. The exact mechanism affecting embryo implantation competency is still unclear. Previous data from our laboratory showed that several members of the let-7 family were up-regulated in the implanting dormant blastocysts and prohibited embryo activation through down-regulation integrin-β3. However, how the mir-let-7 family is regulated is still a question. In this study, the in vitro co-culture model was applied to imitate implantation. Human embryo surrogate Jeg-3 spheroids and endometrium epithelial cells Ishikawa were used. The following views were demonstrated. Firstly,Wnt/β-catenin signaling is essential for Jeg-3 spheroids implantation. Secondly, mir-let-7a is repressed by Wnt signaling, and low let-7a is beneficial for spheroids attachment and outgrowth. Third, in contrast with let-7a, lin28a is up-regulated by Wnt and promotes attachment and outgrowth. Lastly, the function of Wnt in embryo surrogate spheroids in implantation is mediated through lin28a/let-7a axis. In summary, our findings suggest Wnt/β-catenin signaling strength human embryo surrogate spheroids implanting potential through regulation lin28a/let-7a axis.-
dc.languageeng-
dc.publisherAcademic Press. The Journal's web site is located at http://www.elsevier.com/locate/yexcr-
dc.relation.ispartofExperimental Cell Research-
dc.subjectWnt/β-catenin signalling-
dc.subjectLin28a protein-
dc.subjectmir-let-7a-
dc.subjectJeg-3 spheroids-
dc.titleRegulation of human trophoblast surrogate Jeg-3 spheroids implantation potential by Wnt/β-catenin pathway and lin28a/let-7a axis-
dc.typeArticle-
dc.identifier.emailChiu, PCN: pchiucn@hku.hk-
dc.identifier.emailYeung, WSB: wsbyeung@hku.hk-
dc.identifier.emailLiu, W: liuwm@hkucc.hku.hk-
dc.identifier.authorityChiu, PCN=rp00424-
dc.identifier.authorityYeung, WSB=rp00331-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.yexcr.2019.111718-
dc.identifier.pmid31874176-
dc.identifier.scopuseid_2-s2.0-85077643232-
dc.identifier.hkuros319423-
dc.identifier.volume388-
dc.identifier.issue1-
dc.identifier.spagearticle no. 111718-
dc.identifier.epagearticle no. 111718-
dc.identifier.isiWOS:000515211600012-
dc.publisher.placeUnited States-
dc.identifier.issnl0014-4827-

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