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Article: Nucleoplasmic reticulum formation in human endometrial cells is steroid hormone responsive and recruits nascent components

TitleNucleoplasmic reticulum formation in human endometrial cells is steroid hormone responsive and recruits nascent components
Authors
KeywordsNucleoplasmic reticulum
Reproductive cycle
Nuclear architecture
Issue Date2019
Citation
International Journal of Molecular Sciences, 2019, v. 20, n. 23, article no. 5839 How to Cite?
AbstractThe nuclei of cells may exhibit invaginations of the nuclear envelope under a variety of conditions. These invaginations form a branched network termed the nucleoplasmic reticulum (NR), which may be found in cells in pathological and physiological conditions. While an extensive NR is a hallmark of cellular senescence and shows associations with some cancers, very little is known about the formation of NR in physiological conditions, despite the presence of extensive nuclear invaginations in some cell types such as endometrial cells. Here we show that in these cells the NR is formed in response to reproductive hormones. We demonstrate that oestrogen and progesterone are sufficient to induce NR formation and that this process is reversible without cell division upon removal of the hormonal stimulus. Nascent lamins and phospholipids are incorporated into the invaginations suggesting that there is a dedicated machinery for its formation. The induction of NR in endometrial cells offers a new model to study NR formation and function in physiological conditions.
Persistent Identifierhttp://hdl.handle.net/10722/301848
ISSN
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.179
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorPytowski, Lior-
dc.contributor.authorDrozdz, Marek M.-
dc.contributor.authorJiang, Haibo-
dc.contributor.authorHernandez, Zayra-
dc.contributor.authorKumar, Kurun-
dc.contributor.authorKnott, Emily-
dc.contributor.authorVaux, David J.-
dc.date.accessioned2021-08-19T02:20:52Z-
dc.date.available2021-08-19T02:20:52Z-
dc.date.issued2019-
dc.identifier.citationInternational Journal of Molecular Sciences, 2019, v. 20, n. 23, article no. 5839-
dc.identifier.issn1661-6596-
dc.identifier.urihttp://hdl.handle.net/10722/301848-
dc.description.abstractThe nuclei of cells may exhibit invaginations of the nuclear envelope under a variety of conditions. These invaginations form a branched network termed the nucleoplasmic reticulum (NR), which may be found in cells in pathological and physiological conditions. While an extensive NR is a hallmark of cellular senescence and shows associations with some cancers, very little is known about the formation of NR in physiological conditions, despite the presence of extensive nuclear invaginations in some cell types such as endometrial cells. Here we show that in these cells the NR is formed in response to reproductive hormones. We demonstrate that oestrogen and progesterone are sufficient to induce NR formation and that this process is reversible without cell division upon removal of the hormonal stimulus. Nascent lamins and phospholipids are incorporated into the invaginations suggesting that there is a dedicated machinery for its formation. The induction of NR in endometrial cells offers a new model to study NR formation and function in physiological conditions.-
dc.languageeng-
dc.relation.ispartofInternational Journal of Molecular Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectNucleoplasmic reticulum-
dc.subjectReproductive cycle-
dc.subjectNuclear architecture-
dc.titleNucleoplasmic reticulum formation in human endometrial cells is steroid hormone responsive and recruits nascent components-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3390/ijms20235839-
dc.identifier.pmid31757079-
dc.identifier.pmcidPMC6929123-
dc.identifier.scopuseid_2-s2.0-85075284187-
dc.identifier.volume20-
dc.identifier.issue23-
dc.identifier.spagearticle no. 5839-
dc.identifier.epagearticle no. 5839-
dc.identifier.eissn1422-0067-
dc.identifier.isiWOS:000504428300021-

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