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dc.contributor.authorElia, Avraamen
dc.contributor.authorCharalambous, F.en
dc.contributor.authorGeorgiades, Pantelisen
dc.creatorElia, Avraamen
dc.creatorCharalambous, F.en
dc.creatorGeorgiades, Pantelisen
dc.date.accessioned2019-11-04T12:50:32Z
dc.date.available2019-11-04T12:50:32Z
dc.date.issued2011
dc.identifier.issn0006-291X
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53060
dc.description.abstractDuring pregnancy the walls of decidual spiral arteries (SAs) undergo clinically important structural modifications crucial for embryo survival/growth and maternal health. However, the mechanisms of SA remodeling (SAR) are poorly understood. Although an important prerequisite to this understanding is knowledge about the phenotype of SA muscular wall prior to and during the beginning of mouse SAR, this remains largely unexplored and was the main aim of this work. Using histological and immunohistochemical techniques, this study shows for the first time that during early mouse gestation, from embryonic day 7.5 (E7.5) to E10.5, the decidual SA muscular coat is not a homogeneous structure, but consists of two concentric layers. The first is a largely one cell-thick sub-endothelial layer of contractile mural cells (positive for α-smooth muscle actin, calponin and SM22α) with pericyte characteristics (NG2 positive). The second layer is thicker, and evidence is presented that it may be of the synthetic/proliferative smooth muscle phenotype, based on absence (α-smooth muscle actin and calponin) or weak (SM22α) expression of contractile mural cell markers, and presence of synthetic smooth muscle characteristics (expression of non-muscle Myosin heavy chain-IIA and of the cell proliferation marker PCNA). Importantly, immunohistochemistry and morphometrics showed that the contractile mural cell layer although prominent at E7.5-E8.5, becomes drastically reduced by E10.5 and is undetectable by E12.5. In conclusion, this study reveals novel aspects of the decidual SA muscular coat phenotype prior to and during early SAR that may have important implications for understanding the mechanisms of SAR. © 2011 Elsevier Inc.en
dc.sourceBiochemical and biophysical research communicationsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-83055169167&doi=10.1016%2fj.bbrc.2011.11.029&partnerID=40&md5=1a012a1d6281ef56c9e5d59b0abd13a3
dc.subjectarticleen
dc.subjectfemaleen
dc.subjectpriority journalen
dc.subjectgestation perioden
dc.subjectPlacentaen
dc.subjectpregnancyen
dc.subjectprotein expressionen
dc.subjectcell proliferationen
dc.subjectnonhumanen
dc.subjectphenotypeen
dc.subjectAnimalsen
dc.subjectMiceen
dc.subjectanimal experimenten
dc.subjectanimal tissueen
dc.subjectmouseen
dc.subjectcell structureen
dc.subjectCalcium-Binding Proteinsen
dc.subjectMicrofilament Proteinsen
dc.subjectalpha smooth muscle actinen
dc.subjectartery wallen
dc.subjectdeciduaen
dc.subjectMice, Inbred ICRen
dc.subjectDecidua basalisen
dc.subjectMouse pregnancyen
dc.subjectActinsen
dc.subjectArteriesen
dc.subjectcalponinen
dc.subjectimplantationen
dc.subjectMural cellsen
dc.subjectMuscle Contractionen
dc.subjectMuscle Proteinsen
dc.subjectMuscle, Smooth, Vascularen
dc.subjectmyosin heavy chainen
dc.subjectnidationen
dc.subjectpericyteen
dc.subjectSmooth muscleen
dc.subjectSpiral arteryen
dc.subjecttransgelinen
dc.titleNew phenotypic aspects of the decidual spiral artery wall during early post-implantation mouse pregnancyen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.bbrc.2011.11.029
dc.description.volume416
dc.description.startingpage211
dc.description.endingpage216
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 :8</p>en
dc.source.abbreviationBiochem.Biophys.Res.Commun.en
dc.contributor.orcidGeorgiades, Pantelis [0000-0002-5538-3163]
dc.gnosis.orcid0000-0002-5538-3163


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