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dc.contributor.authorCharalambous, F.en
dc.contributor.authorElia, Avraamen
dc.contributor.authorGeorgiades, Pantelisen
dc.creatorCharalambous, F.en
dc.creatorElia, Avraamen
dc.creatorGeorgiades, Pantelisen
dc.date.accessioned2019-11-04T12:50:19Z
dc.date.available2019-11-04T12:50:19Z
dc.date.issued2012
dc.identifier.issn0006-291X
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/52975
dc.description.abstractCircumferential remodeling of spiral arteries (SAs) during pregnancy is crucial for regulating maternal blood flow into the placenta and clinically important. However its mechanism is still ill defined in humans and mice. In mice, several important aspects of decidual SA remodeling (SAR) remain unexplored and were addressed here using morphometrics by examining SAs within the mesometrial half of the decidua basalis between embryonic day 6.5 (E6.5) and midgestation (E10.5). The data presented here provide evidence that supports the following novel conclusions about SAR: (a) SAs (defined by their muscular walls) appear between E6.5 and E7.5, undergo 'outward hypertrophic' SAR (SA lumen widening with muscular wall thickening) during the E7.5-E8.5 and E9.5-E10.5 periods, and 'outward hypotrophic' SAR (SA lumen widening with muscular wall thinning) during the E8.5-E9.5 interval. (b) 'Outward hypotrophic' SAR is associated with decreases in the overall number, but not density, of SA media nuclei, suggesting loss of SA muscular wall cells. Proximity of placenta-derived invasive trophoblast to SAs appears not be involved in SAR, as these cells were undetectable in the mesometrial region of decidua basalis throughout the E6.5-E10.5 period. Although the maternally derived lymphocytes of the decidual uterine natural killer (uNK) cell type are required for decidual SAR, the timing of this, the uNK cell parameter involved and the type of SAR they influence have not been adequately explored. Evidence is presented here that not all decidual SAR during this period is uNK cell-dependent. Rather, the data suggest that uNKs only influence 'outward hypotrophic' SAR during the E8.5-E9.5 period. Evidence is presented that the uNK cell parameter involved is the attainment of a certain maturation state (based on uNK cell size) by SA wall uNKs of the Dolichos biflorus agglutinin (DBA) lectin-positive uNK cell subset. This work also suggests that the previously shown loss of contractile mural cell character from the SA wall does not depend on either uNKs or trophoblast proximity. The novel implications of the present data for early mouse pregnancy are discussed. © 2011 Elsevier Inc.en
dc.sourceBiochemical and biophysical research communicationsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84855834209&doi=10.1016%2fj.bbrc.2011.12.057&partnerID=40&md5=eea3957961e43a6f57835ff3aa95eb18
dc.subjectarticleen
dc.subjectfemaleen
dc.subjectpriority journalen
dc.subjectPlacentaen
dc.subjectpregnancyen
dc.subjectimmunohistochemistryen
dc.subjectnonhumanen
dc.subjectgestational ageen
dc.subjectAnimalsen
dc.subjectMiceen
dc.subjectanimal cellen
dc.subjectanimal tissueen
dc.subjectmouseen
dc.subjectnatural killer cellen
dc.subjectmorphometricsen
dc.subjectlymphocyteen
dc.subjectextracellular matrixen
dc.subjectartery wallen
dc.subjectMusen
dc.subjectdeciduaen
dc.subjectlectinen
dc.subjectcardiovascular functionen
dc.subjectcell maturationen
dc.subjectcell sizeen
dc.subjectDecidua basalisen
dc.subjectDolichos biflorusen
dc.subjectEmbryo Implantationen
dc.subjectKiller Cells, Naturalen
dc.subjectMouse pregnancyen
dc.subjectmuscle cellen
dc.subjectmuscle hypertrophyen
dc.subjectSpiral artery remodelingen
dc.subjectspiral artery remodellingen
dc.subjectTrophoblasten
dc.subjectTrophoblastsen
dc.subjectUNK cellsen
dc.subjectUterine Arteryen
dc.subjectuterusen
dc.titleDecidual spiral artery remodeling during early post-implantation period in mice: Investigation of associations with decidual uNK cells and invasive trophoblasten
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.bbrc.2011.12.057
dc.description.volume417
dc.description.startingpage847
dc.description.endingpage852
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 :15</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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