Chabrat Audrey, Brisson Guillaume, Doucet-Beaupré Hélène, Salesse Charleen, Schaan Profes Marcos, Dovonou Axelle, Akitegetse Cléophace, Charest Julien, Lemstra Suzanne, Côté Daniel, Pasterkamp R Jeroen, Abrudan Monica I, Metzakopian Emmanouil, Ang Siew-Lan, Lévesque Martin
Department of Psychiatry and Neurosciences, Faculty of Medicine, Université Laval, Québec, Quebec, G1V 0A6, Canada.
CERVO Brain Research Centre, 2601, chemin de la Canardière, Québec, Quebec, Canada, G1J 2G3.
Nat Commun. 2017 Oct 16;8(1):933. doi: 10.1038/s41467-017-01042-0.
Mesodiencephalic dopamine neurons play central roles in the regulation of a wide range of brain functions, including voluntary movement and behavioral processes. These functions are served by distinct subtypes of mesodiencephalic dopamine neurons located in the substantia nigra pars compacta and the ventral tegmental area, which form the nigrostriatal, mesolimbic, and mesocortical pathways. Until now, mechanisms involved in dopaminergic circuit formation remained largely unknown. Here, we show that Lmx1a, Lmx1b, and Otx2 transcription factors control subtype-specific mesodiencephalic dopamine neurons and their appropriate axon innervation. Our results revealed that the expression of Plxnc1, an axon guidance receptor, is repressed by Lmx1a/b and enhanced by Otx2. We also found that Sema7a/Plxnc1 interactions are responsible for the segregation of nigrostriatal and mesolimbic dopaminergic pathways. These findings identify Lmx1a/b, Otx2, and Plxnc1 as determinants of dopaminergic circuit formation and should assist in engineering mesodiencephalic dopamine neurons capable of regenerating appropriate connections for cell therapy.Midbrain dopaminergic neurons (mDAs) in the VTA and SNpc project to different regions and form distinct circuits. Here the authors show that transcription factors Lmx1a, Lmx1b, and Otx2 control the axon guidance of mDAs and the segregation of mesolimbic and nigrostriatal dopaminergic pathways.
中脑多巴胺神经元在多种脑功能的调节中发挥核心作用,包括自主运动和行为过程。这些功能由位于黑质致密部和腹侧被盖区的中脑多巴胺神经元的不同亚型提供支持,它们形成了黑质纹状体、中脑边缘和中脑皮质通路。到目前为止,多巴胺能回路形成所涉及的机制在很大程度上仍然未知。在这里,我们表明Lmx1a、Lmx1b和Otx2转录因子控制亚型特异性中脑多巴胺神经元及其适当的轴突支配。我们的结果表明,轴突导向受体Plxnc1的表达受到Lmx1a/b的抑制,并被Otx2增强。我们还发现Sema7a/Plxnc1相互作用负责黑质纹状体和中脑边缘多巴胺能通路的分离。这些发现确定Lmx1a/b、Otx2和Plxnc1是多巴胺能回路形成的决定因素,并应有助于构建能够为细胞治疗再生适当连接的中脑多巴胺神经元。腹侧被盖区和黑质致密部的中脑多巴胺能神经元(mDAs)投射到不同区域并形成不同的回路。在这里,作者表明转录因子Lmx1a、Lmx1b和Otx2控制mDAs的轴突导向以及中脑边缘和黑质纹状体多巴胺能通路的分离。