EphrinB3/EphA4-Mediated Guidance of Ascending and Descending Spinal Tracts
EphrinB3/EphA4-Mediated Guidance of Ascending and Descending Spinal Tracts
The spinal cord contains many descending and ascending longitudinal tracts whose development appears to be controlled by distinct guidance systems. We identified a population of dorsal spinal neurons marked by coexpression of the transcription factor Zic2 and the guidance receptor EphA4. Zic2+;EphA4+ neurons are surrounded by mechanosensory terminals, suggesting innervation by mechanoreceptor afferents. Their axons form an ipsilateral ascending pathway that develops during embryogenesis and projects within the ventral aspect of the dorsal funiculus, the same location as the descending corticospinal tract (CST), which develops postnatally. Interestingly, the same guidance mechanism, namely, ephrinB3-induced EphA4 forward signaling, is required for the guidance of both ascending and descending axon tracts. Our analysis of conditional EphA4 mutant mice also revealed that the development of the dorsal funiculus occurs independently of EphA4 expression in descending CST axons and is linked to the distribution of Zic2+;EphA4+ spinal neurons and the formation of the ascending pathway.
- King’s University United States
- University of Pennsylvania United States
- Max Planck Society Germany
- Max Planck Institute for Biological Intelligence Germany
- Max Planck Institute of Neurobiology Germany
Central Nervous System, Mice, Knockout, Neuroscience(all), Receptor, EphA4, Embryonic Development, Ephrin-B3, Gene Expression Regulation, Developmental, Mice, Transgenic, Axons, Posterior Horn Cells, Mice, Spinal Cord, Cell Tracking, Interneurons, Neural Pathways, Animals, Cells, Cultured, Transcription Factors
Central Nervous System, Mice, Knockout, Neuroscience(all), Receptor, EphA4, Embryonic Development, Ephrin-B3, Gene Expression Regulation, Developmental, Mice, Transgenic, Axons, Posterior Horn Cells, Mice, Spinal Cord, Cell Tracking, Interneurons, Neural Pathways, Animals, Cells, Cultured, Transcription Factors
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