Molecular Mechanisms Controlling the Migration of Striatal Interneurons

• DOI: 10.1523/jneurosci.4317-14.2015
• Publication Date: 2015-06-10T16:35:24Z
• Authors: V. Villar-Cervino; C. Kappeler; S. Nobrega-Pereira; M. Henkemeyer; L. Rago; M. A. Nieto; O. Marin
• Keywords: 570; Receptor, ErbB-4; Receptor, EphB1; Receptor, EphB3; In Vitro Techniques; Striatum; Interneuron; Animals, Genetically Modified; ErbB4; Cerebellar Cortex; Mice; 03 medical and health sciences; Organ Culture Techniques; Cell Movement; Interneurons; 616; Neural Pathways; Animals; Humans; Migration; 0303 health sciences; Gene Expression Regulation, Developmental; Nuclear Proteins; Cell Differentiation; Embryo, Mammalian; Corpus Striatum; Eph; Mice, Inbred C57BL; Mutation; GABAergic

In the developing telencephalon, the medial ganglionic eminence (MGE) generates many cortical and virtually all striatal interneurons. While the molecular mechanisms controlling the migration of interneurons to the cortex have been extensively studied, very little is known about the nature of the signals that guide interneurons to the striatum. Here we report that the allocation of MGE-derived interneurons in the developing striatum of the mouse relies on a combination of chemoattractive and chemorepulsive activities. Specifically, interneurons migrate toward the striatum in response to Nrg1/ErbB4 chemoattraction, and avoid migrating into the adjacent cortical territories by a repulsive activity mediated by EphB/ephrinB signaling. Our results also suggest that the responsiveness of MGE-derived striatal interneurons to these cues is at least in part controlled by the postmitotic activity of the transcription factor Nkx2-1. This study therefore reveals parallel mechanisms for the migration of MGE-derived interneurons to the striatum and the cerebral cortex.