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dc.contributor.authorSağsöz, Hakan
dc.contributor.authorLiman, Narin
dc.contributor.authorAkbalık, M. Erdem
dc.contributor.authorAlan, Emel
dc.contributor.authorSaruhan, Berna Güney
dc.contributor.authorKetani, M. Aydin
dc.contributor.authorErdoğan, Serkan
dc.date.accessioned2023-04-20T08:01:16Z
dc.date.available2023-04-20T08:01:16Z
dc.date.issued2022
dc.identifier.issn0034-5288
dc.identifier.issn1532-2661
dc.identifier.urihttps://doi.org/10.1016/j.rvsc.2022.07.006
dc.identifier.urihttps://hdl.handle.net/20.500.11776/10837
dc.description.abstractThe implantation and placental development processes are regulated with cell adhesion molecules and remod-eling of the maternal endometrium's extracellular matrices (ECM) and fetal chorion. This study aimed to investigate the distribution and localization of some classical cadherins (E-, N-, and P-cadherins) and extracel-lular matrix components collagen type 5 alpha 1, fibronectin, and laminin in the cow placentomes during pregnancy using immunohistochemical and Western blotting analyses. The study results confirmed the expression of E- and P-cadherins, collagen type V alpha 1 (COLV alpha 1), fibronectin, and laminin in the cow placentomes, but not N-cadherin. Throughout the pregnancy, E-and P-cadherins, COLV alpha 1, and laminin were localized in the luminal and glan-dular epithelium of the inter-caruncular endometrium, caruncular epithelium, and the uninucleate (UNCs) and binucleate trophoblast giant cells (BNCs/TGCs). E- cadherin immunoreactivity in the first pregnancy period was strong in the UNCs while moderate in the BNCs/TGCs. However, it was weak in both trophoblast in the second and third pregnancy periods. In the fetal trophoblasts, P-cadherin and laminin immunostainings were more intense in the BNCs/TGCs than UNCs. The fetal and maternal stromal cells were also positive for P-cadherin, COLV alpha 1, fibronectin, and laminin. The immunostaining intensity of COLV alpha 1 and fibronectin in the stromal extracellular matrix of the placentomes decreased as the pregnancy progressed. The endothelia of fetal and maternal vessels were positive for all proteins. The presence and distinct localization of cadherins and ECM proteins in the cow placentome components support the role of these molecules in regulating placental cell growth, migration, and matrix production during pregnancy.en_US
dc.description.sponsorshipScientific and Technological Research Council of Turkey [TUBITAK ARDEB 1002, 116O797]en_US
dc.description.sponsorshipFunding This work was supported by the the Scientific and Technological Research Council of Turkey (TUBITAK ARDEB 1002 Grant No. 116O797) .en_US
dc.language.isoengen_US
dc.publisherElsevier Sci Ltden_US
dc.identifier.doi10.1016/j.rvsc.2022.07.006
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBovineen_US
dc.subjectCollagenen_US
dc.subjectLamininen_US
dc.subjectN-Cadherinen_US
dc.subjectPlacentaen_US
dc.subjectUterusen_US
dc.subjectCollagen-Type-Ien_US
dc.subjectExtracellular-Matrixen_US
dc.subjectAdhesion Moleculesen_US
dc.subjectBeta-Cateninen_US
dc.subjectV Collagenen_US
dc.subjectCell-Differentiationen_US
dc.subjectIntegrin Receptorsen_US
dc.subjectHuman Trophoblasten_US
dc.subjectBovine Placentaen_US
dc.subjectFibronectinen_US
dc.titleExpression of cadherins and some connective tissue components in cow uterus and placenta during pregnancyen_US
dc.typearticleen_US
dc.relation.ispartofResearch In Veterinary Scienceen_US
dc.departmentFakülteler, Veteriner Fakültesi, Temel Bilimler Bölümü, Anatomi Ana Bilim Dalıen_US
dc.identifier.volume151en_US
dc.identifier.startpage64en_US
dc.identifier.endpage79en_US
dc.institutionauthorErdoğan, Serkan
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid56521500300
dc.authorscopusid6602085918
dc.authorscopusid35114425000
dc.authorscopusid35301900800
dc.authorscopusid9842574500
dc.authorscopusid6602579282
dc.authorscopusid36650778800
dc.authorwosidErdoğan, Serkan/F-5923-2011
dc.identifier.wosWOS:000843032800006en_US
dc.identifier.scopus2-s2.0-85134826246en_US
dc.identifier.pmid35870371en_US


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