Cargando…

Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections

The cerebellum is a brain region responsible for motor coordination and for refining motor programs. While a great deal is known about the structure and connectivity of the mammalian cerebellum, fundamental questions regarding its function in behavior remain unanswered. Recently, the zebrafish has e...

Descripción completa

Detalles Bibliográficos
Autores principales: Heap, Lucy A., Goh, Chi Ching, Kassahn, Karin S., Scott, Ethan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3612595/
https://www.ncbi.nlm.nih.gov/pubmed/23554587
http://dx.doi.org/10.3389/fncir.2013.00053
_version_ 1782264671647039488
author Heap, Lucy A.
Goh, Chi Ching
Kassahn, Karin S.
Scott, Ethan K.
author_facet Heap, Lucy A.
Goh, Chi Ching
Kassahn, Karin S.
Scott, Ethan K.
author_sort Heap, Lucy A.
collection PubMed
description The cerebellum is a brain region responsible for motor coordination and for refining motor programs. While a great deal is known about the structure and connectivity of the mammalian cerebellum, fundamental questions regarding its function in behavior remain unanswered. Recently, the zebrafish has emerged as a useful model organism for cerebellar studies, owing in part to the similarity in cerebellar circuits between zebrafish and mammals. While the cell types composing their cerebellar cortical circuits are generally conserved with mammals, zebrafish lack deep cerebellar nuclei, and instead a majority of cerebellar output comes from a single type of neuron: the eurydendroid cell. To describe spatial patterns of cerebellar output in zebrafish, we have used genetic techniques to label and trace eurydendroid cells individually and en masse. We have found that cerebellar output targets the thalamus and optic tectum, and have confirmed the presence of pre-synaptic terminals from eurydendroid cells in these structures using a synaptically targeted GFP. By observing individual eurydendroid cells, we have shown that different medial-lateral regions of the cerebellum have eurydendroid cells projecting to different targets. Finally, we found topographic organization in the connectivity between the cerebellum and the optic tectum, where more medial eurydendroid cells project to the rostral tectum while lateral cells project to the caudal tectum. These findings indicate that there is spatial logic underpinning cerebellar output in zebrafish with likely implications for cerebellar function.
format Online
Article
Text
id pubmed-3612595
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-36125952013-04-01 Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections Heap, Lucy A. Goh, Chi Ching Kassahn, Karin S. Scott, Ethan K. Front Neural Circuits Neuroscience The cerebellum is a brain region responsible for motor coordination and for refining motor programs. While a great deal is known about the structure and connectivity of the mammalian cerebellum, fundamental questions regarding its function in behavior remain unanswered. Recently, the zebrafish has emerged as a useful model organism for cerebellar studies, owing in part to the similarity in cerebellar circuits between zebrafish and mammals. While the cell types composing their cerebellar cortical circuits are generally conserved with mammals, zebrafish lack deep cerebellar nuclei, and instead a majority of cerebellar output comes from a single type of neuron: the eurydendroid cell. To describe spatial patterns of cerebellar output in zebrafish, we have used genetic techniques to label and trace eurydendroid cells individually and en masse. We have found that cerebellar output targets the thalamus and optic tectum, and have confirmed the presence of pre-synaptic terminals from eurydendroid cells in these structures using a synaptically targeted GFP. By observing individual eurydendroid cells, we have shown that different medial-lateral regions of the cerebellum have eurydendroid cells projecting to different targets. Finally, we found topographic organization in the connectivity between the cerebellum and the optic tectum, where more medial eurydendroid cells project to the rostral tectum while lateral cells project to the caudal tectum. These findings indicate that there is spatial logic underpinning cerebellar output in zebrafish with likely implications for cerebellar function. Frontiers Media S.A. 2013-04-01 /pmc/articles/PMC3612595/ /pubmed/23554587 http://dx.doi.org/10.3389/fncir.2013.00053 Text en Copyright © 2013 Heap, Goh, Kassahn and Scott. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Heap, Lucy A.
Goh, Chi Ching
Kassahn, Karin S.
Scott, Ethan K.
Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections
title Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections
title_full Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections
title_fullStr Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections
title_full_unstemmed Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections
title_short Cerebellar Output in Zebrafish: An Analysis of Spatial Patterns and Topography in Eurydendroid Cell Projections
title_sort cerebellar output in zebrafish: an analysis of spatial patterns and topography in eurydendroid cell projections
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3612595/
https://www.ncbi.nlm.nih.gov/pubmed/23554587
http://dx.doi.org/10.3389/fncir.2013.00053
work_keys_str_mv AT heaplucya cerebellaroutputinzebrafishananalysisofspatialpatternsandtopographyineurydendroidcellprojections
AT gohchiching cerebellaroutputinzebrafishananalysisofspatialpatternsandtopographyineurydendroidcellprojections
AT kassahnkarins cerebellaroutputinzebrafishananalysisofspatialpatternsandtopographyineurydendroidcellprojections
AT scottethank cerebellaroutputinzebrafishananalysisofspatialpatternsandtopographyineurydendroidcellprojections