LH-dependent steroid production and protein phosphorylation in culture of rat tumour Leydig cells.

The possible cause of the decreased responsiveness of cultured Leydig cells to stimulation with LH was investigated with rat tumour Leydig cells cultured at 32 degrees C for 2 days. Pregnenolone production and phosphorylation of proteins were studied in combination with the activity of cyclic AMP-dependent protein kinase. Pregnenolone production in cultured tumour Leydig cells decreased from 45 +/- 16 on day 0 to 14 +/- 7 on day 2 (ng/60 min/mg protein) under basal conditions and from 226 +/- 108 on day 0 to 30 +/- 24 on day 2 (ng/60 min/ng protein) under LH-stimulated conditions (means +/- SD, n = 4). This decrease may be accounted for by decreased capacity of cholesterol side-chain cleavage which decreased (in the presence of 25-hydroxycholesterol) from 1.68 +/- 0.26 on day 0 to 0.74 +/- 0.48 on day 2 (microgram/60 min/mg protein; mean +/- SD, n = 4) and decreased activity of cyclic AMP-dependent protein kinase (as apparent from a direct assay of protein kinase activity and the extent of phosphorylation of LH-dependent phosphoproteins).