Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/56524
Full metadata record
DC FieldValueLanguage
dc.contributor.authorÇil, N.-
dc.contributor.authorFenkçi, İ.V.-
dc.contributor.authorMete, G.A.-
dc.contributor.authorMutlu, D.-
dc.contributor.authorKabukçu, C.-
dc.contributor.authorÇabuş, Ü.-
dc.date.accessioned2024-01-30T14:31:10Z-
dc.date.available2024-01-30T14:31:10Z-
dc.date.issued2024-
dc.identifier.issn1309-9833-
dc.identifier.urihttps://doi.org/10.31362/patd.1346146-
dc.identifier.urihttps://hdl.handle.net/11499/56524-
dc.description.abstractPurposoe: Cell surface proteins known as Siglecs exhibit a specific affinity for sialic acid. Primarily located on the surface of immune cells, Siglecs belong to the subset of lectins called I-type lectins. Siglecs have important roles in maternal-fetal immune tolerance. We aimed to analyze the expression of Siglecs on Human Villous Trophoblasts (HVT) cells. Materials and methods: Total RNA was extracted from the HVT cell line, cDNA was synthesized, and real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) was performed the determine the changes in Siglec-3,-5,-6,-7,-8,-9,-10,-11, and-16 mRNA levels. In addition, Siglec levels were assessed by using immunohistochemical staining. Immunoreactivity against Siglec-6 and Siglec-9 was evaluated separately according to the intensity of brown color. Results: Expression levels of Siglec genes by qRT-PCR and melting curve analyses were performed using RNA extracted from the HVT cell line. Siglec-3,-5,-6,-7,-9,-10,-11, and-16 genes were found to be expressed in the HVT cell line. Differently, Siglec-8 results were undetected after cycle 40, which was considered a negative result. The immunocytochemical examination of the HVT cell line revealed that Siglec-6 expression was moderate in the cytoplasm (Score:2). Siglec-9 expression was prominent in the cytoplasm (Score:3). Conclusion: The results showed that Siglec-6 and Siglec-9 were expressed more than other Siglec proteins in the human trophoblast cells. Immunocytochemistry results also support these findings. Our study is the first to show Siglec-9 expression in human trophoblast cells. © 2024, Pamukkale University. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherPamukkale Universityen_US
dc.relation.ispartofPamukkale Medical Journalen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjecthuman villous trophoblastsen_US
dc.subjectsialic aciden_US
dc.subjectSiglecsen_US
dc.titleExpression of Sialic Acid Binding Receptors (Siglecs) in human trophoblast cell lineen_US
dc.title.alternativeİnsan Trofoblast Hücre Hattında Sialik Asit Bağlayıcı Reseptörlerin (Siglecs) Ekspresyonuen_US
dc.typeArticleen_US
dc.identifier.volume17en_US
dc.identifier.issue2en_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.31362/patd.1346146-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid55392501500-
dc.authorscopusid6507701460-
dc.authorscopusid6507766696-
dc.authorscopusid57212511655-
dc.authorscopusid6506758719-
dc.authorscopusid56690382800-
dc.identifier.scopus2-s2.0-85180653512en_US
dc.identifier.trdizinid1231322en_US
dc.institutionauthor-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
item.openairetypeArticle-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.01. Surgical Medicine-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.01. Surgical Medicine-
crisitem.author.dept14.01. Surgical Medicine-
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
Show simple item record



CORE Recommender

Page view(s)

58
checked on Aug 24, 2024

Download(s)

18
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.