首页> 外文期刊>The Journal of Biochemistry >Orphan nuclear receptor Nur77 accelerates the initial phase of adipocyte differentiation in 3T3-L1 cells by promoting mitotic clonal expansion.
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Orphan nuclear receptor Nur77 accelerates the initial phase of adipocyte differentiation in 3T3-L1 cells by promoting mitotic clonal expansion.

机译:孤儿核受体Nur77通过促进有丝分裂克隆扩增,加速3T3-L1细胞中脂肪细胞分化的初始阶段。

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摘要

Nur77 is an orphan member of the nuclear receptor superfamily that is expressed in various types of cells and mediates diverse biological processes. Although Nur77 mRNA is induced in the early stage of adipogenesis of 3T3-L1 cells, its roles are not known. To address this issue, we closely inspected the expression of Nur77 mRNA and protein during differentiation of 3T3-L1 cells. Nur77 was induced rapidly and transiently at both mRNA and protein levels only in the initial phase of differentiation induction, and localized almost exclusively in the nuclei. Isobutylmethylxanthine was essential for the induction of Nur77 protein, acting by at least in part protecting the protein from rapid degradation by proteasome. Nur77 siRNA resulted in delayed adipogenesis in 3T3-L1, accompanied by retarded mitotic clonal expansion. These effects were mediated at least partly by decreased expression of cyclins D and E. Constitutive expression of Nur77 inhibited adipogenesis of 3T3-L1, accompanied by enhanced expression of cyclin D1 and prolonged mitotic clonal expansion. Moreover, constitutive expression of Nur77 inhibited, but transient induction of Nur77 promoted, adipogenesis in NIH-3T3 cells. These results suggest that Nur77 accelerates adipocyte differentiation by regulating cell cycle progression and the rapid and transient induction is crucial for its action.
机译:Nur77是核受体超家族的一个孤儿,它在各种类型的细胞中表达并介导多种生物学过程。尽管Nur77 mRNA在3T3-L1细胞成脂的早期阶段被诱导,但其作用尚不清楚。为了解决这个问题,我们仔细检查了3T3-L1细胞分化过程中Nur77 mRNA和蛋白的表达。 Nur77仅在分化诱导的初始阶段就在mRNA和蛋白质水平上都被迅速而短暂地诱导,并且几乎只定位于细胞核中。异丁基甲基黄嘌呤对于Nur77蛋白的诱导是必不可少的,其作用至少是部分地保护了该蛋白免遭蛋白酶体的快速降解。 Nur77 siRNA导致3T3-L1中的脂肪形成延迟,并伴随着有丝分裂克隆扩张的延迟。这些作用至少部分地由细胞周期蛋白D和E的表达降低来介导。Nur77的组成型表达抑制3T3-L1的脂肪形成,并伴随着细胞周期蛋白D1的表达增强和有丝分裂克隆的扩展。此外,Nur77的组成型表达被抑制,但Nur77的瞬时诱导促进了NIH-3T3细胞的脂肪形成。这些结果表明,Nur77通过调节细胞周期进程来加速脂肪细胞分化,而快速而短暂的诱导对其作用至关重要。

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