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Am J Physiol Endocrinol Metab (February 15, 2005). doi:10.1152/ajpendo.00563.2004
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Submitted on November 29, 2004
Accepted on February 9, 2005

Alpha-2 To Beta-3 Adrenoceptor Switch In 3T3- L1 Preadipocytes And Adipocytes: Modulation By Testosterone, 17{beta}-Estradiol And Progesterone

Marta Monjo1, Esperanza Pujol1, and Pilar Roca1*

1 Grup de Metabolisme Energetic i Nutricio. Departament de Biologia Fonamental i Ciencies de la Salut. Institut Universitari d'Investigacio en Ciencies de la Salut (IUNICS), Universitat de les Illes Balears, Palma de Mallorca, Illes Balears, Spain

* To whom correspondence should be addressed. E-mail: pilar.roca{at}uib.es.

Sex steroid hormones are important factors in the determination of fat distribution and accumulation. The aim of this study was to investigate the effect of testosterone (T), 17{beta}- estradiol (17{beta}E) and progesterone (P) on adrenergic receptor (AR) gene expression in 3T3-L1 preadipocytes and adipocytes, and their relation to the proliferation and differentiation processes. Our data clearly show that {alpha}2A-AR was the highest AR subtype expressed in preadipocytes, whereas in mature adipocytes was by far {beta}3-AR. In the differentiation process to adipocytes, {alpha}2AAR expression was decreased to 0.3 fold (p<0.01), whereas {beta}3-AR was upregulated by 578 fold (p<0.001), compared to preadipocytes. In addition, the expression of {alpha}2A-AR in preadipocytes was increased upon incubation with T, 17{beta}E and P, and a stimulation of proliferation was also observed in 17{beta}E and P treated cells. In mature adipocytes, 17{beta}E and P enhanced both {alpha}2A- and {beta}3-AR gene expression - although the effects on {beta}3-AR mRNA levels could be more relevant as {beta}3-AR was the most highly expressed -, while T only increased {alpha}2A-AR mRNA levels. Leptin and aP2/FABP mRNA levels were higher after 17{beta}E and P treatment, possibly indicating a proadipogenic effect of these hormones. In conclusion, this study indicates that AR gene expression is affected by these hormones both in preadipocytes and adipocytes, which could have potential importance when considering the role of ARs in the mechanisms underlying the genderrelated differences in adipose tissue regional distribution.




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