I. Berthaut et al., HUMAN PROSTATIC CELLS IN CULTURE - DIFFERENT TESTOSTERONE METABOLIC PROFILE IN EPITHELIAL-CELLS AND FIBROBLASTS FROM NORMAL OR HYPERPLASTICPROSTATES, Journal of steroid biochemistry and molecular biology, 58(2), 1996, pp. 235-242
The prostate gland depends on androgens for its development and the ma
intainance of its differentiated structures and secretory function. We
have characterized the metabolic pathways of testosterone in isolated
epithelial (NE) and fibroblast cultured cells from normal (NF) and hy
perplastic (BPHF) prostates, in order to provide a tool for the study
of androgen function in the prostate in defined conditions. In NE, 5 a
lpha-reductase (5 alpha-R) is the predominant metabolic pathway wherea
s in NF 17 beta-hydroxysteroid dehydrogenase (17 beta-OHSDHase) is the
main activity. However, 5 alpha-R in NF is 5-10-fold higher than in N
E. Furthermore, a striking increase in both enzyme activities is obser
ved in fibroblasts from hyperplastic prostates (5 alpha-R x 8; 17 beta
-OHSDHase x 250 relative to NF). Delta 4-androstenedione coud serve as
a reservoir for testosterone or could be a tentative protective mecha
nism directing testosterone metabolism towards an inactive molecule. I
n conclusion, human epithelial and stromal cells maintain in culture t
heir main metabolic characteristics. The knowledge derived from these
studies should facilitate the reconstitution and analysis of their int
eractions, which in vivo may modify their respective metabolism. Copyr
ight (C) 1996 Elsevier Science Ltd.