Testosterone and progesterone metabolism in the human neuroblastoma cell line SH-SY5Y

Abstract

The ability of the human neuroblastoma cell line SH-SY5Y to metabolize androgens and progesterone was studied by incubating the cells in the presence of labeled testosterone (T) or progesterone (P) to measure, respectively, the formation of dihydrotestosterone (DHT) or dihydroprogesterone (DHP) (5α-reductase activitiy). The 3α-hydroxysteroid dehydrogenase activity was studied by evaluating the conversion of labeled DHT into 5α-androstan-3α, 17β-diol (3α-diol). The results show that undifferentiated neuroblastoma cells posses a significant 5α-reductase activity, as shown by the considerable conversion of T into DHT; moreover, this enzymatic activity seems to be significantly stimulated following cell differentiation induced by the phorbol ester TPA, but not after differentiation induced by retinoic acid (RA). The 5α-reductase(s) present in SH-SY5Y cells is also able to convert P into DHP. In undifferentiated cells, this conversion was about 8 times higher than that of T into DHT. Under the influences of TPA and RA, the formation of DHP followed the same pattern observed for the formation of DHT. SH-SY5Y cells also appear to possess the enzyme 3α-hydroxysteroid dehydrogenase, since they are able to convert DHT into 3α-diol. This enzymatic activity is not altered following TPA-induced differentiation and appears to be decreased following treatment with RA. It is suggested that the SH-SY5Y cell line may represent a useful “ in vitro” model for the study of the mechanisms involved in the control of androgen and P metabolism in nervous cells.