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Ephrin-A5调节中脑多巴胺能上行通路的形成。

Ephrin-A5 regulates the formation of the ascending midbrain dopaminergic pathways.

作者信息

Cooper Margaret A, Kobayashi Kazuto, Zhou Renping

机构信息

Department of Chemical Biology, Ernest P. Mario School of Pharmacy, Rutgers University, Piscataway, New Jersey 08854, USA.

出版信息

Dev Neurobiol. 2009 Jan;69(1):36-46. doi: 10.1002/dneu.20685.

Abstract

Dopaminergic neurons from the substantia nigra and the ventral tegmental area of the midbrain project to the caudate/putamen and nucleus accumbens, respectively, establishing the mesostriatal and the mesolimbic pathways. However, the mechanisms underlying the development of these pathways are not well understood. In the current study, the EphA5 receptor and its corresponding ligand, ephrin-A5, were shown to regulate dopaminergic axon outgrowth and influence the formation of the midbrain dopaminergic pathways. Using a strain of mutant mice in which the EphA5 cytoplasmic domain was replaced with beta-galactosidase, EphA5 protein expression was detected in both the ventral tegmental area and the substantia nigra of the midbrain. Ephrin-A5 was found in both the dorsolateral and the ventromedial regions of the striatum, suggesting a role in mediating dopaminergic axon-target interactions. In the presence of ephrin-A5, dopaminergic neurons extended longer neurites in in vitro coculture assays. Furthermore, in mice lacking ephrin-A5, retrograde tracing studies revealed that fewer neurons sent axons to the striatum. These observations indicate that the interactions between ephrin-A ligands and EphA receptors promote growth and targeting of the midbrain dopaminergic axons to the striatum.

摘要

来自中脑黑质和腹侧被盖区的多巴胺能神经元分别投射到尾状核/壳核和伏隔核,形成了中脑纹状体通路和中脑边缘通路。然而,这些通路发育的潜在机制尚未完全清楚。在当前研究中,EphA5受体及其相应配体ephrin-A5被证明可调节多巴胺能轴突的生长,并影响中脑多巴胺能通路的形成。利用一种将EphA5胞质结构域替换为β-半乳糖苷酶的突变小鼠品系,在中脑的腹侧被盖区和黑质中均检测到了EphA5蛋白表达。在纹状体的背外侧和腹内侧区域均发现了ephrin-A5,这表明其在介导多巴胺能轴突与靶标的相互作用中发挥作用。在体外共培养实验中,在有ephrin-A5存在的情况下,多巴胺能神经元伸出的神经突更长。此外,在缺乏ephrin-A5的小鼠中,逆行示踪研究显示,向纹状体发送轴突的神经元数量减少。这些观察结果表明,ephrin-A配体与EphA受体之间的相互作用促进了中脑多巴胺能轴突向纹状体的生长和靶向。

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