Various stimulators of the cyclic AMP pathway fail to promote adipose conversion of porcine preadipocytes in primary culture

Citation
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
Citations number
48
Categorie Soggetti
Cell & Developmental Biology
Journal title
DIFFERENTIATION
ISSN journal
03014681 → ACNP
Volume
64
Issue
5
Year of publication
1999
Pages
255 - 262
Database
ISI
SICI code
0301-4681(199906)64:5<255:VSOTCA>2.0.ZU;2-I
Abstract
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.