Center for Neurobiology Research, Fralin Biomedical Research Institute at Virginia Tech Carilion, Roanoke, United States; Graduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Blacksburg, United States
Katelyn Stebbins
Center for Neurobiology Research, Fralin Biomedical Research Institute at Virginia Tech Carilion, Roanoke, United States; Graduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Blacksburg, United States; Virginia Tech Carilion School of Medicine, Roanoke, United States
Ellen C Gingrich
Department of Biology, Drexel University, Philadelphia, United States; Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, United States
Hehuang Xie
Fralin Life Sciences Institute at Virginia Tech, Blacksburg, United States; School of Neuroscience, College of Science, Virginia Tech, Blacksburg, United States; Genetics, Bioinformatics and Computational Biology Program, Virginia Tech, Blacksburg, United States; Department of Biomedical Sciences and Pathobiology, Virginia–Maryland College of Veterinary Medicine, Blacksburg, United States
John N Campbell
Department of Biology, University of Virginia, Charlottesville, United States; Neuroscience Graduate Program, University of Virginia, Charlottesville, United States
Department of Biology, Drexel University, Philadelphia, United States; Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, United States
Center for Neurobiology Research, Fralin Biomedical Research Institute at Virginia Tech Carilion, Roanoke, United States; School of Neuroscience, College of Science, Virginia Tech, Blacksburg, United States; Department of Biological Sciences, College of Science, Virginia Tech, Blacksburg, United States; Department of Pediatrics, Virginia Tech Carilion School of Medicine, Roanoke, United States
Axons of retinal ganglion cells (RGCs) play critical roles in the development of inhibitory circuits in visual thalamus. We previously reported that RGC axons signal astrocytes to induce the expression of fibroblast growth factor 15 (FGF15), a motogen required for GABAergic interneuron migration into visual thalamus. However, how retinal axons induce thalamic astrocytes to generate Fgf15 and influence interneuron migration remains unknown. Here, we demonstrate that impairing RGC activity had little impact on interneuron recruitment into mouse visual thalamus. Instead, our data show that retinal-derived sonic hedgehog (SHH) is essential for interneuron recruitment. Specifically, we show that thalamus-projecting RGCs express SHH and thalamic astrocytes generate downstream components of SHH signaling. Deletion of RGC-derived SHH leads to a significant decrease in Fgf15 expression, as well as in the percentage of interneurons recruited into visual thalamus. Overall, our findings identify a morphogen-dependent neuron–astrocyte signaling mechanism essential for the migration of thalamic interneurons.