| Literature DB >> 32562661 |
Sara Brignani1, Divya D A Raj1, Ewoud R E Schmidt1, Özge Düdükcü1, Youri Adolfs1, Anna A De Ruiter1, Mateja Rybiczka-Tesulov1, Marieke G Verhagen1, Christiaan van der Meer1, Mark H Broekhoven1, Juan A Moreno-Bravo2, Laurens M Grossouw1, Emilie Dumontier3, Jean-François Cloutier3, Alain Chédotal2, R Jeroen Pasterkamp4.
Abstract
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.Entities:
Keywords: GABAergic neuron; Netrin-1; development; dopamine neuron; fluorescent light sheet microscopy; guidance cue; intersectional genetics; migration; neuronal subtype; substantia nigra
Year: 2020 PMID: 32562661 DOI: 10.1016/j.neuron.2020.05.037
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173