C. Boone et al., Various stimulators of the cyclic AMP pathway fail to promote adipose conversion of porcine preadipocytes in primary culture, DIFFERENTIA, 64(5), 1999, pp. 255-262
The cyclic adenosine-monophosphate (cAMP) pathway is generally recognized a
s one of the essential pathways for the adipose conversion of rodent preadi
pocytes in vitro. However, divergent effects of cAMP on adipocyte different
iation have also been reported. Since there is very little data on non-rode
nt preadipose cells, the aim of the present work was to analyze the effects
of classic activators of the cAMP pathway on the proliferation and differe
ntiation of porcine preadipocytes grown either in serum-free or in serum-co
ntaining medium. In both media, the addition of 10 mu M forskolin from day
1 after cell plating to day 3 or 7 did not affect cell proliferation. Such
stimulations also failed to enhance preadipocyte differentiation, as assess
ed by the measurement of lipoprotein lipase (LPL) and glycerol 3-phosphate
dehydrogenase (GPDH) activities, two markers of adipose conversion. Similar
results were obtained when various concentrations of forskolin (0.1 nM-100
mu M) were added for 2 days either during the growth phase (days 1-3) or a
fter confluence (days 5-7). Addition of methylisobutylxanthine (MIX) or 8-b
romo-cAMP was also found inefficient to stimulate porcine preadipocytes dif
ferentiation clearly. By contrast, post-confluence treatment of the murine
3T3-L1 cell line with either forskolin or MIX markedly enhanced lipid accum
ulation and led to a dramatic increase in GPDH activity (up to 120 times).
This indicates that similar culture conditions are adipogenic for the murin
e 3T3-L1 preadipocytes but not for porcine preadipose cells. In summary, th
is work clearly highlights the finding that porcine preadipocytes do not re
spond to classic activators of the cAMP pathway like rodent cells do. This
calls in question again the general model proposed for the action of this p
athway in adipose conversion and suggests that the mechanisms regulating ad
ipocyte differentiation may differ among species.