Teneurin-3 specifies morphological and functional connectivity of retinal ganglion cells in the vertebrate visual system
- Authors
- Antinucci, P., Nikolaou, N., Meyer, M.P., and Hindges, R.
- ID
- ZDB-PUB-131202-11
- Date
- 2013
- Source
- Cell Reports 5(3): 582-592 (Journal)
- Registered Authors
- Hindges, Robert, Meyer, Martin, Nikolaou, Nikolas
- Keywords
- none
- MeSH Terms
-
- Animals
- Animals, Genetically Modified
- Gene Knockdown Techniques
- Microscopy, Confocal
- Nerve Tissue Proteins/biosynthesis
- Nerve Tissue Proteins/genetics
- Nerve Tissue Proteins/metabolism*
- Neurons/metabolism
- Neurons/physiology
- Retinal Ganglion Cells/metabolism
- Retinal Ganglion Cells/physiology*
- Visual Pathways/physiology*
- Zebrafish
- Zebrafish Proteins/biosynthesis
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 24183672 Full text @ Cell Rep.
A striking feature of the CNS is the precise wiring of its neuronal connections. During vertebrate visual system development, different subtypes of retinal ganglion cells (RGCs) form specific connections with their corresponding synaptic partners. However, the underlying molecular mechanisms remain to be fully elucidated. Here, we report that the cell-adhesive transmembrane protein Teneurin-3 (Tenm3) is required by zebrafish RGCs for acquisition of their correct morphological and functional connectivity in vivo. Teneurin-3 is expressed by RGCs and their presynaptic amacrine and postsynaptic tectal cell targets. Knockdown of Teneurin-3 leads to RGC dendrite stratification defects within the inner plexiform layer, as well as mistargeting of dendritic processes into outer portions of the retina. Moreover, a subset of RGC axons exhibits tectal laminar arborization errors. Finally, functional analysis of RGCs targeting the tectum reveals a selective deficit in the development of orientation selectivity after Teneurin-3 knockdown. These results suggest that Teneurin-3 plays an instructive role in the functional wiring of the vertebrate visual system.