Development and activation of immune cells are submitted to hormonal influe
nces, as illustrated by the roles of corticosteroids in thymus, pregnancy-r
elated estrogens in B-cell development, or prolactin (PRL) on T-cell genera
tion and function. We have analyzed the putative role of PRL in B lymphopoi
esis and differentiation. We chose as an experimental model the interleukin
(IL)-3 dependent BaF-3 pro-B cell line, which was transfected with the rat
long form of the PRL receptor (PRL-R) and transferred from IL-3- to PRL-en
riched media, When stimulated with PRL, the PRL-R transfectants underwent s
ome changes characteristic of B-cell differentiation: (a) IL-2R alpha chain
became positively controlled by PRL; (b) antiapoptotic Bcl-2 protein was i
nduced by PRL in a dose-dependent manner; and (c) transcription of the pre-
B cell receptor encoding the lambda 5 gene was strongly up-regulated. We at
tempted to evaluate the differentiation-promoting activity of PRL in more p
hysiological conditions, and the presence of PRL-R in bone marrow B-cell pr
ecursors was revealed, Furthermore, PRL promoted significant expansions of
defined B-lineage cell populations in short-term bone marrow cell cultures.
These findings suggest that PRL, in collaboration with other cytokines and
hormonal influences, modulates B-cell development.