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.