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 behaviour remain unanswered. Recently, the zebrafish ha...

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Main Authors: Lucy eHeap, Chi-Ching eGoh, Karin S Kassahn, Ethan K Scott
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-04-01
Series:Frontiers in Neural Circuits
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncir.2013.00053/full
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spelling doaj-99eb5fc2b5fa44208c928dff8c31b7502020-11-25T00:44:49ZengFrontiers Media S.A.Frontiers in Neural Circuits1662-51102013-04-01710.3389/fncir.2013.0005345793Cerebellar output in zebrafish: an analysis of spatial patterns and topography in eurydendroid cell projectionsLucy eHeap0Chi-Ching eGoh1Karin S Kassahn2Ethan K Scott3Ethan K Scott4The University of QueenslandThe University of QueenslandThe University of QueenslandThe University of QueenslandThe University of QueenslandThe 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 behaviour 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 cerebellar cortical circuits are generally conserved, zebrafish lack deep cerebellar nuclei, and instead a bulk 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 presynaptic 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 organisation 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.http://journal.frontiersin.org/Journal/10.3389/fncir.2013.00053/fullCerebellumThalamusZebrafishoptic tectumtopographyeurydendroid
collection DOAJ
language English
format Article
sources DOAJ
author Lucy eHeap
Chi-Ching eGoh
Karin S Kassahn
Ethan K Scott
Ethan K Scott
spellingShingle Lucy eHeap
Chi-Ching eGoh
Karin S Kassahn
Ethan K Scott
Ethan K Scott
Cerebellar output in zebrafish: an analysis of spatial patterns and topography in eurydendroid cell projections
Frontiers in Neural Circuits
Cerebellum
Thalamus
Zebrafish
optic tectum
topography
eurydendroid
author_facet Lucy eHeap
Chi-Ching eGoh
Karin S Kassahn
Ethan K Scott
Ethan K Scott
author_sort Lucy eHeap
title 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_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_sort cerebellar output in zebrafish: an analysis of spatial patterns and topography in eurydendroid cell projections
publisher Frontiers Media S.A.
series Frontiers in Neural Circuits
issn 1662-5110
publishDate 2013-04-01
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 behaviour 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 cerebellar cortical circuits are generally conserved, zebrafish lack deep cerebellar nuclei, and instead a bulk 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 presynaptic 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 organisation 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.
topic Cerebellum
Thalamus
Zebrafish
optic tectum
topography
eurydendroid
url http://journal.frontiersin.org/Journal/10.3389/fncir.2013.00053/full
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AT chichingegoh cerebellaroutputinzebrafishananalysisofspatialpatternsandtopographyineurydendroidcellprojections
AT karinskassahn cerebellaroutputinzebrafishananalysisofspatialpatternsandtopographyineurydendroidcellprojections
AT ethankscott cerebellaroutputinzebrafishananalysisofspatialpatternsandtopographyineurydendroidcellprojections
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