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Cytosporone B is an agonist for nuclear orphan receptor Nur77

机译:Cytosporone B是核孤儿受体Nur77的激动剂

摘要

Nuclear orphan receptor Nur77 has important roles in many biological processes. However, a physiological ligand for Nur77 has not been identified. Here, we report that the octaketide cytosporone B (Csn-B) is a naturally occurring agonist for Nur77. Csn-B specifically binds to the ligand-binding domain of Nur77 and stimulates Nur77-dependent transactivational activity towards target genes including Nr4a1 (Nur77) itself, which contains multiple consensus response elements allowing positive autoregulation in a Csn-B-dependent manner. Csn-B also elevates blood glucose levels in fasting C57 mice, an effect that is accompanied by induction of multiple genes involved in gluconeogenesis. These biological effects were not observed in Nur77-null (Nr4a1(-/-)) mice, which indicates that Csn-B regulates gluconeogenesis through Nur77. Moreover, Csn-B induced apoptosis and retarded xenograft tumor growth by inducing Nur77 expression, translocating Nur77 to mitochondria to cause cytochrome c release. Thus, Csn-B may represent a promising therapeutic drug for cancers and hypoglycemia, and it may also be useful as a reagent to increase understanding of Nur77 biological function.
机译:核孤儿受体Nur77在许多生物学过程中都具有重要作用。然而,尚未鉴定出Nur77的生理配体。在这里,我们报告的ococeptide cytosporone B(Csn-B)是Nur77的天然激动剂。 Csn-B特异性结合Nur77的配体结合结构域,并刺激针对包括Nr4a1(Nur77)本身在内的靶基因的Nur77依赖性反式激活活性,该靶基因包含多个共有应答元件,允许以Csn-B依赖性方式进行积极的自动调节。 Csn-B还可以提高空腹C57小鼠的血糖水平,这种作用伴随着涉及糖异生的多个基因的诱导。在Nur77无效(Nr4a1(-/-))小鼠中未观察到这些生物学效应,这表明Csn-B通过Nur77调节糖异生。此外,Csn-B通过诱导Nur77表达,将Nur77转运至线粒体以引起细胞色素c释放,从而诱导细胞凋亡并延迟异种移植肿瘤的生长。因此,Csn-B可能代表癌症和低血糖的有前途的治疗药物,它也可以用作增加对Nur77生物学功能的了解的试剂。

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