Adipocyte differentiation is inhibited by melatonin through the regulation of C/EBP beta transcriptional activity


Autoria(s): ALONSO-VALE, Maria Isabel Cardoso; PERES, Sidney Barnabe; VERNOCHET, Cecile; FARMER, Stephen R.; LIMA, Fabio Bessa
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Considering that melatonin has been implicated in body weight control, this work investigated whether this effect involves the regulation of adipogenesis. 3T3-L1 preadipocytes were induced to differentiate in the absence or presence of melatonin (10(-3) m). Swiss-3T3 cells ectopically and conditionally (Tet-off system) over-expressing the 34 kDa C/EBP beta isoform (Swiss-LAP cells) were employed as a tool to assess the mechanisms of action at the molecular level. Protein markers of the adipogenic phenotype were analyzed by Western blot. At 36 hr of differentiation of 3T3-L1 preadipocytes, a reduction of PPAR gamma expression was detected followed by a further reduction, at day 4, of perilipin, aP2 and adiponectin protein expression in melatonin-treated cells. Real-time PCR analysis also showed a decrease of PPAR gamma (60%), C/EBP alpha (75%), adiponectin (30%) and aP2 (40%) mRNA expression. Finally, we transfected Swiss LAP cells with a C/EBP alpha gene promoter/reporter construct in which luciferase expression is enhanced in response to C/EBP beta activity. Culture of such transfected cells in the absence of tetracycline led to a 2.5-fold activation of the C/EBP alpha promoter. However, when treated with melatonin, the level of C/EBP alpha promoter activation by C/EBP beta was reduced by 50% (P = 0.05, n = 6). In addition, this inhibitory effect of melatonin was also reflected in the phenotype of the cells, since their capacity to accumulate lipids droplets was reduced as confirmed by the poor staining with Oil Red O. In conclusion, melatonin at a concentration of 10(-3) m works as a negative regulator of adipogenesis acting in part by inhibiting the activity of a critical adipogenic transcription factor, C/EBP beta.

Sao Paulo State Research Foundation (FAPESP)[04/06767-2]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Sao Paulo State Research Foundation (FAPESP)[04/14696-8]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Sao Paulo State Research Foundation (FAPESP)[07/50404-0]

Identificador

JOURNAL OF PINEAL RESEARCH, v.47, n.3, p.221-227, 2009

0742-3098

http://producao.usp.br/handle/BDPI/28065

10.1111/j.1600-079X.2009.00705.x

http://dx.doi.org/10.1111/j.1600-079X.2009.00705.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL PUBLISHING, INC

Relação

Journal of Pineal Research

Direitos

closedAccess

Copyright WILEY-BLACKWELL PUBLISHING, INC

Palavras-Chave #adipogenesis #C #EBP beta #CEBP alpha #melatonin #PPAR gamma #ACTIVATED RECEPTOR-GAMMA #ADIPOSE-TISSUE ADAPTABILITY #BODY-WEIGHT #PPAR-GAMMA #3T3-L1 PREADIPOCYTES #GENE PROMOTER #PLASMA LEPTIN #PINEAL-GLAND #FOOD-INTAKE #ADIPOGENESIS #Endocrinology & Metabolism #Neurosciences #Physiology
Tipo

article

original article

publishedVersion