PUBLICATION
Hardwiring of fine synaptic layers in the zebrafish visual pathway
- Authors
- Nevin, L.M., Taylor, M.R., and Baier, H.
- ID
- ZDB-PUB-081218-37
- Date
- 2008
- Source
- Neural Development 3: 36 (Journal)
- Registered Authors
- Baier, Herwig, Nevin, Linda, Taylor, Michael
- Keywords
- none
- MeSH Terms
-
- Animals
- Choline O-Acetyltransferase/metabolism
- Green Fluorescent Proteins/chemistry
- Immunohistochemistry/methods
- Neurons/cytology
- Neurons/metabolism*
- Neuropil/cytology
- Neuropil/metabolism*
- Parvalbumins/metabolism
- Protein Kinase C-delta/metabolism
- Retina/anatomy & histology
- Retina/cytology
- Retina/metabolism*
- Signal Transduction
- Superior Colliculi/anatomy & histology
- Superior Colliculi/cytology
- Superior Colliculi/metabolism*
- Visual Pathways/anatomy & histology
- Visual Pathways/metabolism*
- Zebrafish*
- PubMed
- 19087349 Full text @ Neural Dev.
Citation
Nevin, L.M., Taylor, M.R., and Baier, H. (2008) Hardwiring of fine synaptic layers in the zebrafish visual pathway. Neural Development. 3:36.
Abstract
BACKGROUND: Neuronal connections are often arranged in layers, which are divided into sublaminae harboring synapses with similar response properties. It is still debated how fine-grained synaptic layering is established during development. Here we investigated two stratified areas of the zebrafish visual pathway, the inner plexiform layer (IPL) of the retina and the neuropil of the optic tectum, and determined if activity is required for their organization. RESULTS: The IPL of 5-day-old zebrafish larvae is composed of at least nine sublaminae, comprising the connections between different types of amacrine, bipolar, and ganglion cells (ACs, BCs, GCs). These sublaminae were distinguished by their expression of cell type-specific transgenic fluorescent reporters and immunohistochemical markers, including protein kinase CSZ (PKC), parvalbumin (Parv), zrf3, and choline acetyltransferase (ChAT). In the tectum, four retinal input layers abut a laminated array of neurites of tectal cells, which differentially express PKC and Parv. We investigated whether these patterns were affected by experimental disruptions of retinal activity in developing fish. Neither elimination of light inputs by dark rearing, nor a D,L-amino-phosphono-butyrate-induced reduction in the retinal response to light onset (but not offset) altered IPL or tectal lamination. Moreover, thorough elimination of chemical synaptic transmission with Botulinum toxin B left laminar synaptic arrays intact. CONCLUSIONS: Our results call into question a role for activity-dependent mechanisms - instructive light signals, balanced on and off BC activity, Hebbian plasticity, or a permissive role for synaptic transmission - in the synaptic stratification we examined. We propose that genetically encoded cues are sufficient to target groups of neurites to synaptic layers in this vertebrate visual system.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping