D. Lacasa et al., RAT PREADIPOCYTE ADENYLYL-CYCLASE - INFLUENCE OF FAT LOCALIZATION ANDANDROGENIC STATUS, Biochimica et biophysica acta. Molecular cell research, 1224(3), 1994, pp. 527-532
The influence of androgenic status on basal and stimulated cAMP produc
tion, adenylyl cyclase activities and immunoblot quantified G(s alpha)
and G(i alpha 2) subunits of the adenylyl cyclase regulatory proteins
were compared in confluent preadipocytes from subcutaneous (SC) and d
eep-intraabdominal (epididymal) fat deposits. Maximal cAMP response to
isoproterenol was lower in SC than in epididymal preadipocytes. After
castration, this site-specific difference was suppressed. cAMP respon
se to 2-chloroadenosine, which was identical in the two types of pread
ipocytes, was decreased by castration in epididymal cells but not in S
C cells. The catalytic activity of adenylyl cyclase and its maximal re
sponse to GTP were higher in epididymal than in SC preadipocytes. This
response to GTP was decreased by castration in epididymal preadipocyt
es while it remained unchanged in SC preadipocytes. The catalytic acti
vity of adenylyl cyclase was unchanged by androgenic status whatever t
he cell localization. Levels of G(s alpha) quantified by immunoblottin
g were not modified whatever the androgenic status and cell origine. L
evels of Gi alpha 2 were not affected by the androgenic status as well
, but were lower in SC than in epididymal cells. This study shows that
components of the adenylyl cyclase system in preadipocytes are differ
ently regulated by the androgenic status depending on the anatomical o
rigin of the cells.