PROLACTIN RECEPTOR EXPRESSION BY SPLENOCYTES FROM RATS IN VARIOUS HORMONAL STATES

Citation
H. Gunes et al., PROLACTIN RECEPTOR EXPRESSION BY SPLENOCYTES FROM RATS IN VARIOUS HORMONAL STATES, Cell proliferation, 30(3-4), 1997, pp. 127-137
Citations number
31
Categorie Soggetti
Cell Biology
Journal title
ISSN journal
09607722
Volume
30
Issue
3-4
Year of publication
1997
Pages
127 - 137
Database
ISI
SICI code
0960-7722(1997)30:3-4<127:PREBSF>2.0.ZU;2-I
Abstract
Prolactin (PRL) is mitogenic for lymphocytes in vitro, but the respons iveness of lymphocytes depends on the in vivo hormonal status of the r ats from which the cells were obtained. Lymphocytes from ovariectomize d (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 lympho cyte responsiveness to prolactin and levels of cell surface prolactin receptors (PRL-R) expression, the percentage of splenocytes and each s plenocyte subpopulation expressing surface PRL-R from rats of various hormonal states (OVX, oestradiol-injected OVX, oestrus and male) was a nalysed by single-colour and dual-colour flow cytometric analysis. We found that approximately 20% of splenocytes expressed surface PRL-R re gardless of hormonal states (n=16). The majority (85%) of PRL-R positi ve splenocytes were B lymphocytes whereas 11.1% and 4.8% of splenocyte s expressing the PRL-R were CD4 positive T-helper (T-H) and CD8 positi ve T-cytotoxic (T-C) lymphocytes, respectively. B lymphocytes also sta ined more brightly than T lymphocytes. This distribution of PRL-R expr ession did not show significant alterations on total splenocytes or T- H and T-C lymphocytes during various hormonal stages. However, the per centage of PRL-R-positive B lymphocytes increased markedly in OVX rats (twofold), compared to rats at oestrus. In summary, no correlation wa s found between the responsiveness to prolactin as a mitogen and level s of PRL-R expression by lymphocytes from rats at different hormonal s tates. This result suggests that sex steroid hormones may control prol actin responsiveness of lymphocytes by affecting the signal transducti on pathway through PRL-R rather than by altering the level of the cell surface receptor expression.