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dc.contributor.authorCharalambous, Christinaen
dc.contributor.authorDrakou, Katerinaen
dc.contributor.authorNicolaou, Stavrosen
dc.contributor.authorGeorgiades, Pantelisen
dc.creatorCharalambous, Christinaen
dc.creatorDrakou, Katerinaen
dc.creatorNicolaou, Stavrosen
dc.creatorGeorgiades, Pantelisen
dc.date.accessioned2019-11-04T12:50:19Z
dc.date.available2019-11-04T12:50:19Z
dc.date.issued2013
dc.identifier.issn1932-8486
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/52971
dc.description.abstractAlthough spatiotemporal changes of the glycome (full set of glycans, otherwise known as saccharides or carbohydrates) during placenta formation (placentation) are functionally and clinically important, they are poorly defined. Here, we elucidated novel aspects of the glycome during mouse placentation, from embryonic day 6.5 (E6.5) to E12.5, by investigating the largely unexplored binding distribution of lectin I from Bandeiraea simplicifolia (BS-I lectin), a glycan-binding protein that recognizes the DGalNAc and DGal glycans found at the terminal ends of specific oligosaccharides attached to lipids or proteins. We show that BS-I lectin binding marks all trophoblast cells during early placentation (E7.5 and E8.5 stages), continues in labyrinthine and junctional zone trophoblast but is lost from parietal trophoblast giant cells by E10.5/E11.5 (definitive placenta stage) and is lost from all trophoblast types, but marks the fetal capillary endothelium of the labyrinth, by E12.5. In the decidua basalis (the maternal part of the placenta), BS-I lectin positivity mainly marks the decidual stroma cells of the venous sinusoid area (E7.5 and E8.5 stages) and the entire decidua basalis by E10.5, as well as the osteopontin-positive subset of uterine natural killer (uNK) cells from E7.5 onwards. This work provides the first comprehensive description of the hitherto ill-defined spatiotemporal binding distribution of BS-I lectin in the fetal and maternal placenta between E6.5 and E12.5, thereby contributing to glycome elucidation during placentation. It also establishes BS-I lectin positivity as a novel pan-trophoblast marker during early placentation and as a new marker for mature uNK cells from E7.5 onwards. © 2013 Wiley Periodicals, Inc.en
dc.sourceAnatomical Recorden
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84878106796&doi=10.1002%2far.22698&partnerID=40&md5=75c973fed93c1f31c7039608c6441df7
dc.subjectarticleen
dc.subjectFemaleen
dc.subjectcontrolled studyen
dc.subjectpriority journalen
dc.subjectPlacentaen
dc.subjectPregnancyen
dc.subjectunclassified drugen
dc.subjectnonhumanen
dc.subjectAnimalsen
dc.subjectMiceen
dc.subjectanimal cellen
dc.subjectanimal experimenten
dc.subjectmouseen
dc.subjectnatural killer cellen
dc.subjectprotein bindingen
dc.subjectstroma cellen
dc.subjectMurinaeen
dc.subjectinner earen
dc.subjectBandeiraea simplicifoliaen
dc.subjectBandeiraea simplicifolia lectin Ien
dc.subjectcapillary endotheliumen
dc.subjectcarbohydrateen
dc.subjectCarbohydrate Metabolismen
dc.subjectdeciduaen
dc.subjectGlycomeen
dc.subjectGlycomicsen
dc.subjectlectinen
dc.subjectMice, Inbred ICRen
dc.subjectPlacentationen
dc.subjectPlant Lectinsen
dc.subjectreproductionen
dc.subjecttrophoblasten
dc.subjectTrophoblast developmenten
dc.subjectuNK cellsen
dc.titleNovel spatiotemporal glycome changes in the murine placenta during placentation based on BS-I lectin binding patternsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/ar.22698
dc.description.volume296
dc.description.startingpage921
dc.description.endingpage932
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :1</p>en
dc.source.abbreviationAnat.Rec.en
dc.contributor.orcidGeorgiades, Pantelis [0000-0002-5538-3163]
dc.gnosis.orcid0000-0002-5538-3163


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