Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Cortical interneurons in rodents are generated in the ventral telencephalon and migrate tangentially into the cortex. This process requires the coordinated action of many intrinsic and extrinsic factors. Here we show that Robo1 and Robo2 receptor proteins are dynamically expressed throughout the period of corticogenesis and colocalize with interneuronal markers, suggesting that they play a role in the migration of these cells. Analysis of Robo mutants showed a marked increase in the number of interneurons in the cortices of Robo1(-/-), but not Robo2(-/-), animals throughout the period of corticogenesis and in adulthood; this excess number of interneurons was observed in all layers of the developing cortex. Using BrdU incorporation in dissociated cell cultures and phosphohistone-3 labeling in vivo, we demonstrated that the increased number of interneurons in Robo1(-/-) mice is, at least in part, due to increased proliferation. Interestingly, a similar increase in proliferation was observed in Slit1(-/-)/Slit2(-/-) mutant mice, suggesting that cell division is influenced by Slit-Robo signaling mechanisms. Morphometric analysis of migrating interneurons in Robo1(-/-), Robo2(-/-) and Slit1(-/-)/Slit2(-/-), but not in Slit1(-/-) mice, showed a differential increase in neuronal process length and branching suggesting that Slit-Robo signaling also plays an important role in the morphological differentiation of these neurons.

Original publication




Journal article


Dev Biol

Publication Date





648 - 658


Animals, Biomarkers, Calbindins, Cell Culture Techniques, Cell Differentiation, Cell Movement, Cell Proliferation, Cells, Cultured, Cerebral Cortex, DNA, Complementary, Electroporation, Embryo, Mammalian, Embryonic Stem Cells, Genetic Markers, Genetic Vectors, Genomic Library, Immunohistochemistry, Integrases, Intercellular Signaling Peptides and Proteins, Interneurons, Kinetics, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Mutation, Nerve Tissue Proteins, Receptors, Immunologic, S100 Calcium Binding Protein G, Selection, Genetic, Signal Transduction, Telencephalon, Transfection