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在发育中的脑干中,神经纤毛蛋白1是Nurr1的直接下游靶点。

Neuropilin1 is a direct downstream target of Nurr1 in the developing brain stem.

作者信息

Hermanson Elisabet, Borgius Lotta, Bergsland Maria, Joodmardi Eliza, Perlmann Thomas

机构信息

Ludwig Institute for Cancer Research, Stockholm Branch, Stockholm, Sweden.

出版信息

J Neurochem. 2006 Jun;97(5):1403-11. doi: 10.1111/j.1471-4159.2006.03829.x. Epub 2006 Apr 21.

Abstract

The orphan nuclear receptor Nurr1 is expressed in the developing and adult central nervous system. Previous studies have shown that Nurr1 is essential for the generation of midbrain dopamine neurons. Furthermore, Nurr1 is critical for respiratory functions associated with the brain stem. Very few Nurr1 regulated genes have been identified and it remains unclear how Nurr1 influences the function and development of neurons. To identify novel Nurr1 target genes we have searched for regulated genes in the dopaminergic MN9D cell line. These experiments identified Neuropilin-1 (Nrp1), a receptor protein involved in axon guidance and angiogenesis, as a novel Nurr1 target gene. Nrp1 expression was rapidly up-regulated by Nurr1 in MN9D cells and in situ hybridization analysis showed that Nrp1 was coexpressed with Nurr1 in the brain stem dorsal motor nucleus. Importantly, Nrp1 expression was down-regulated in this area in Nurr1 null mice. Moreover, two functional Nurr1 binding sites were identified in the Nrp1 promoter and Nurr1 was found to be recruited to these sites in MN9D cells, further supporting that Nrp1 is a direct downstream target of Nurr1. Taken together, our findings suggest that Nurr1 might influence the processes of axon guidance and/or angiogenesis via the regulation of Nrp1 expression.

摘要

孤儿核受体Nurr1在发育中的和成年的中枢神经系统中表达。先前的研究表明,Nurr1对于中脑多巴胺神经元的生成至关重要。此外,Nurr1对于与脑干相关的呼吸功能也很关键。目前仅鉴定出极少数受Nurr1调控的基因,Nurr1如何影响神经元的功能和发育仍不清楚。为了鉴定新的Nurr1靶基因,我们在多巴胺能MN9D细胞系中寻找受调控的基因。这些实验确定神经纤毛蛋白-1(Nrp1),一种参与轴突导向和血管生成的受体蛋白,为新的Nurr1靶基因。在MN9D细胞中,Nurr1可迅速上调Nrp1的表达,原位杂交分析表明,在脑干背运动核中Nrp1与Nurr1共表达。重要的是,在Nurr1基因敲除小鼠的该区域中,Nrp1的表达下调。此外,在Nrp1启动子中鉴定出两个功能性Nurr1结合位点,并且发现Nurr1在MN9D细胞中被募集至这些位点,进一步证明Nrp1是Nurr1的直接下游靶标。综上所述,我们的研究结果表明,Nurr1可能通过调控Nrp1的表达来影响轴突导向和/或血管生成过程。

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