Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/4501
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dc.contributor.authorGüneş, Hatice-
dc.contributor.authorZawilla, S.-
dc.contributor.authorMastro, Andrea M.-
dc.date.accessioned2016-04-01T08:17:05Z-
dc.date.available2016-04-01T08:17:05Z-
dc.date.issued1997-
dc.identifier.citationGüneş, H., Zawilla, S., and Mastro, A. M. (1997). Prolactin receptor expression by splenocytes from rats in various hormonal states. Cell Proliferation, 30(4), 127-137. doi:10.1111/j.1365-2184.1997.tb00929.xen_US
dc.identifier.issn0960-7722-
dc.identifier.urihttp://doi.org/10.1111/j.1365-2184.1997.tb00929.x-
dc.identifier.urihttp://hdl.handle.net/11147/4501-
dc.description.abstractProlactin (PRL) is mitogenic for lymphocytes in vitro, but the responsiveness of lymphocytes depends on the in vivo hormonal status of the rats from which the cells were obtained. Lymphocytes from ovariectomized (OVX) rats, but not from rats in oestrus or from male rats, respond to prolactin; administration of oestradiol to OVX rats diminishes the response. In order to determine if a correlation exists between lymphocyte responsiveness to prolactin and levels of cell surface prolactin receptors (PRL-R) expression, the percentage of splenocytes and each splenocyte subpopulation expressing surface PRL-R from rats of various hormonal states (OVX, oestradiol-injected OVX, oestrus and male) was analysed by single-colour and dual-colour flow cytometric analysis. We found that approximately 20% of splenocytes expressed surface PRL-R regardless of hormonal states (n = 16). The majority (85%) of PRL-R positive splenocytes were B lymphocytes whereas 11.1% and 4.8% of splenocytes expressing the PRL-R were CD4 positive T-helper (TH) and CD8 positive T-cytotoxic (TC) lymphocytes, respectively. B lymphocytes also stained more brightly than T lymphocytes. This distribution of PRL-R expression did not show significant alterations on total splenocytes or TH and TC lymphocytes during various hormonal stages. However, the percentage of PRL-R-positive B lymphocytes increased markedly in OVX rats (twofold), compared to rats at oestrus. In summary, no correlation was found between the responsiveness to prolactin as a mitogen and levels of PRL-R expression by lymphocytes from rats at different hormonal states. This result suggests that sex steroid hormones may control prolactin responsiveness of lymphocytes by affecting the signal transduction pathway through PRL-R rather than by altering the level of the cell surface receptor expression.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Inc.en_US
dc.relation.ispartofCell Proliferationen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectProlactin receptoren_US
dc.subjectAnimal cellen_US
dc.titleProlactin receptor expression by splenocytes from rats in various hormonal statesen_US
dc.typeArticleen_US
dc.authoridTR2082en_US
dc.institutionauthorGüneş, Hatice-
dc.departmentİzmir Institute of Technology. Molecular Biology and Geneticsen_US
dc.identifier.volume30en_US
dc.identifier.issue4en_US
dc.identifier.startpage127en_US
dc.identifier.endpage137en_US
dc.identifier.wosWOS:A1997YE28300004en_US
dc.identifier.scopus2-s2.0-0030830822en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1111/j.1365-2184.1997.tb00929.x-
dc.identifier.pmid9375025en_US
dc.relation.doi10.1111/j.1365-2184.1997.tb00929.xen_US
dc.coverage.doi10.1111/j.1365-2184.1997.tb00929.xen_US
dc.identifier.wosqualityQ3-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.grantfulltextopen-
item.openairetypeArticle-
crisitem.author.dept04.03. Department of Molecular Biology and Genetics-
Appears in Collections:Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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