BACKGROUND. We demonstrated that p53-deficiency is sufficient for the estab
lishment of clonal cell lines from the uterus and prostate. In the present
study, we improved cloning methods to establish androgen-responsive cell li
nes.
METHODS. In our previous study, a prostatic cell line was established from
the ventral prostate of a p53-deficient mouse and was maintained in a mediu
m containing heat-inactivated fetal calf serum at 10% supplemented with ins
ulin (10 mug/ml), transferrin (10 mug/ml), cholera toxin (10 ng/ml) and sel
enium (10(-8) M). In the present study, 5x-dihydrotestosterone (10(-8) M) w
as added to the medium from the beginning of cloning procedures.
RESULTS. We succeeded in the establishment of an androgen receptor positive
prostatic cell line, designated PEES. PEAS cells exhibited a typical epith
elial morphology in culture and growth was stimulated by androgens in a dos
e-dependent manner. In addition, they grew and formed three-dimensional str
uctures in collagen gel, in which growth was also stimulated by androgen.
CONCLUSIONS. Although PEAS lacks p53 gene, it still retains androgen sensit
ivity. In collagen gel culture, PEAS cells fan grow and form three-dimensio
nal structures similar to those of the primary cultures reported previously
. Furthermore, prostates of p53-deficient mice are shown to be useful sourc
es for obtaining androgen-responsive cells lines. (C) 2001 Wiley-Liss,Inc.