Previous studies have shown that the hamster CYP11B2 gene promoter is under
the influence of angiotensin II (AII), cAMP and potassium (K+). However, v
ery little is known about the mechanisms by which these compounds regulate
the transcription of the CYP11B2 gene. Therefore we analysed the 5'-flankin
g region of the hamster CYP11B2 gene using a transient transfection express
ion system in NCI-H295 adrenocortical cells, which are known to respond to
K+, cAMP and AII. The first 486 bp before the transcription initiation site
were introduced upstream of the chloramphenicol acetyl transferase gene. N
CI-H295 cells transfected with this - 486 construct showed increased CAT ac
tivity upon treatment by K+, AII, forskolin and cAMP. The calcium channel a
ntagonist nifedipine partially blocked the enhancing effects of AII, forsko
lin and cAMP by 35%, 30% and 30% respectively, whereas it completely blacke
d the stimulatory effects of KCl (1). These results thus show the involveme
nt of calcium channels in the regulation of CYP11B2 gene transcription by K
+, and their partial involvement in the regulation of this gene by AII, for
skolin and cAMP in NCI-H295 cells.