Department of Translational Neuroscience, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Universiteitsweg 100, 3584 CG Utrecht, the Netherlands.
Institut de la Vision, Sorbonne Université, INSERM, CNRS, 17 Rue Moreau, 75012 Paris, France.
Neuron. 2020 Aug 19;107(4):684-702.e9. doi: 10.1016/j.neuron.2020.05.037. Epub 2020 Jun 19.
The midbrain dopamine (mDA) system is composed of molecularly and functionally distinct neuron subtypes that mediate specific behaviors and show select disease vulnerability, including in Parkinson's disease. Despite progress in identifying mDA neuron subtypes, how these neuronal subsets develop and organize into functional brain structures remains poorly understood. Here we generate and use an intersectional genetic platform, Pitx3-ITC, to dissect the mechanisms of substantia nigra (SN) development and implicate the guidance molecule Netrin-1 in the migration and positioning of mDA neuron subtypes in the SN. Unexpectedly, we show that Netrin-1, produced in the forebrain and provided to the midbrain through axon projections, instructs the migration of GABAergic neurons into the ventral SN. This migration is required to confine mDA neurons to the dorsal SN. These data demonstrate that neuron migration can be controlled by remotely produced and axon-derived secreted guidance cues, a principle that is likely to apply more generally.
中脑多巴胺(mDA)系统由分子和功能上不同的神经元亚型组成,介导特定的行为,并表现出特定的疾病易感性,包括帕金森病。尽管在鉴定 mDA 神经元亚型方面取得了进展,但这些神经元亚群如何发育并组织成功能性脑结构仍然知之甚少。在这里,我们生成并使用了一种交叉遗传平台 Pitx3-ITC,以剖析黑质(SN)发育的机制,并表明神经导向分子 Netrin-1 参与了 SN 中 mDA 神经元亚型的迁移和定位。出乎意料的是,我们发现 Netrin-1 在前脑中产生,并通过轴突投射提供给中脑,指导 GABA 能神经元向 SN 的腹侧迁移。这种迁移对于将 mDA 神经元限制在 SN 的背侧是必需的。这些数据表明,神经元迁移可以通过远程产生和轴突衍生的分泌导向线索来控制,这一原则可能更普遍地适用。