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孤儿核受体NR4A家族对于脂肪生成并非必需。

The NR4A family of orphan nuclear receptors are not required for adipogenesis.

作者信息

Au W-S, Payne V A, O'Rahilly S, Rochford J J

机构信息

Department of Clinical Biochemistry, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.

出版信息

Int J Obes (Lond). 2008 Feb;32(2):388-92. doi: 10.1038/sj.ijo.0803763. Epub 2007 Dec 11.

DOI:10.1038/sj.ijo.0803763
PMID:18071346
Abstract

Nuclear hormone receptors of the NR4A subfamily are rapidly induced during the early stages of adipogenesis, leading to the speculation that they may have important roles in this process. One of the three subfamily members, Nur77 has also been shown to play key roles in energy expenditure and lipolysis in skeletal muscle and in the control of hepatic gluconeogenesis. We, therefore, examined the role of NR4A factors in adipogenesis using the well-characterized 3T3-L1 preadipocyte model. Inhibition of Nur77 expression using siRNA did not affect induction of adipogenic genes, nor the accumulation of lipid. To inhibit the activity of all the three NR4A family members, we generated preadipocytes stably expressing a well-characterized dominant-negative Nur77 (DN-Nur77), known to block the function of the other NR4A factors, Nurr1 and Nor1, as well as Nur77. While the increased NR4A activity observed following adipogenic induction was completely abolished in these cells, DN-Nur77 expression did not affect the expression of genes characteristic of terminally differentiated adipocytes and had no impact on lipid accumulation in these cells. Thus, while members of the NR4A subfamily of nuclear receptors may have important metabolic roles in skeletal muscle and liver, we demonstrate that they are dispensable for normal adipocyte development.

摘要

NR4A亚家族的核激素受体在脂肪生成的早期阶段会迅速被诱导产生,这引发了人们对于它们可能在这一过程中发挥重要作用的猜测。该亚家族的三个成员之一,Nur77,也已被证明在骨骼肌的能量消耗和脂肪分解以及肝脏糖异生的调控中发挥关键作用。因此,我们使用特征明确的3T3-L1前脂肪细胞模型,研究了NR4A因子在脂肪生成中的作用。使用小干扰RNA(siRNA)抑制Nur77的表达,既不影响脂肪生成基因的诱导,也不影响脂质的积累。为了抑制所有三个NR4A家族成员的活性,我们构建了稳定表达一种特征明确的显性负性Nur77(DN-Nur77)的前脂肪细胞,已知这种DN-Nur77会阻断其他NR4A因子Nurr1和Nor1以及Nur77的功能。虽然在这些细胞中,脂肪生成诱导后观察到的NR4A活性增加被完全消除,但DN-Nur77的表达并不影响终末分化脂肪细胞特征性基因的表达,也不影响这些细胞中的脂质积累。因此,虽然核受体NR4A亚家族的成员可能在骨骼肌和肝脏中具有重要的代谢作用,但我们证明它们对于正常脂肪细胞的发育并非必不可少。

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