Cargando…

Presynaptic Calcium Signalling in Cerebellar Mossy Fibres

Whole-cell recordings were obtained from mossy fibre terminals in adult turtles in order to characterize the basic membrane properties. Calcium imaging of presynaptic calcium signals was carried out in order to analyse calcium dynamics and presynaptic GABA B inhibition. A tetrodotoxin (TTX)-sensitiv...

Descripción completa

Detalles Bibliográficos
Autores principales: Thomsen, Louiza B., Jörntell, Henrik, Midtgaard, Jens
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821199/
https://www.ncbi.nlm.nih.gov/pubmed/20162034
http://dx.doi.org/10.3389/neuro.04.001.2010
_version_ 1782177418693312512
author Thomsen, Louiza B.
Jörntell, Henrik
Midtgaard, Jens
author_facet Thomsen, Louiza B.
Jörntell, Henrik
Midtgaard, Jens
author_sort Thomsen, Louiza B.
collection PubMed
description Whole-cell recordings were obtained from mossy fibre terminals in adult turtles in order to characterize the basic membrane properties. Calcium imaging of presynaptic calcium signals was carried out in order to analyse calcium dynamics and presynaptic GABA B inhibition. A tetrodotoxin (TTX)-sensitive fast Na(+) spike faithfully followed repetitive depolarizing pulses with little change in spike duration or amplitude, while a strong outward rectification dominated responses to long-lasting depolarizations. High-threshold calcium spikes were uncovered following addition of potassium channel blockers. Calcium imaging using Calcium-Green dextran revealed a stimulus-evoked all-or-none TTX-sensitive calcium signal in simple and complex rosettes. All compartments of a complex rosette were activated during electrical activation of the mossy fibre, while individual simple and complex rosettes along an axon appeared to be isolated from one another in terms of calcium signalling. CGP55845 application showed that GABA B receptors mediated presynaptic inhibition of the calcium signal over the entire firing frequency range of mossy fibres. A paired-pulse depression of the calcium signal lasting more than 1 s affected burst firing in mossy fibres; this paired-pulse depression was reduced by GABA B antagonists. While our results indicated that a presynaptic rosette electrophysiologically functioned as a unit, topical GABA application showed that calcium signals in the branches of complex rosettes could be modulated locally, suggesting that cerebellar glomeruli may be dynamically sub-compartmentalized due to ongoing inhibition mediated by Golgi cells. This could provide a fine-grained control of mossy fibre-granule cell information transfer and synaptic plasticity within a mossy fibre rosette.
format Text
id pubmed-2821199
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Frontiers Research Foundation
record_format MEDLINE/PubMed
spelling pubmed-28211992010-02-16 Presynaptic Calcium Signalling in Cerebellar Mossy Fibres Thomsen, Louiza B. Jörntell, Henrik Midtgaard, Jens Front Neural Circuits Neuroscience Whole-cell recordings were obtained from mossy fibre terminals in adult turtles in order to characterize the basic membrane properties. Calcium imaging of presynaptic calcium signals was carried out in order to analyse calcium dynamics and presynaptic GABA B inhibition. A tetrodotoxin (TTX)-sensitive fast Na(+) spike faithfully followed repetitive depolarizing pulses with little change in spike duration or amplitude, while a strong outward rectification dominated responses to long-lasting depolarizations. High-threshold calcium spikes were uncovered following addition of potassium channel blockers. Calcium imaging using Calcium-Green dextran revealed a stimulus-evoked all-or-none TTX-sensitive calcium signal in simple and complex rosettes. All compartments of a complex rosette were activated during electrical activation of the mossy fibre, while individual simple and complex rosettes along an axon appeared to be isolated from one another in terms of calcium signalling. CGP55845 application showed that GABA B receptors mediated presynaptic inhibition of the calcium signal over the entire firing frequency range of mossy fibres. A paired-pulse depression of the calcium signal lasting more than 1 s affected burst firing in mossy fibres; this paired-pulse depression was reduced by GABA B antagonists. While our results indicated that a presynaptic rosette electrophysiologically functioned as a unit, topical GABA application showed that calcium signals in the branches of complex rosettes could be modulated locally, suggesting that cerebellar glomeruli may be dynamically sub-compartmentalized due to ongoing inhibition mediated by Golgi cells. This could provide a fine-grained control of mossy fibre-granule cell information transfer and synaptic plasticity within a mossy fibre rosette. Frontiers Research Foundation 2010-02-08 /pmc/articles/PMC2821199/ /pubmed/20162034 http://dx.doi.org/10.3389/neuro.04.001.2010 Text en Copyright © 2010 Thomsen, Jörntell and Midtgaard. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Thomsen, Louiza B.
Jörntell, Henrik
Midtgaard, Jens
Presynaptic Calcium Signalling in Cerebellar Mossy Fibres
title Presynaptic Calcium Signalling in Cerebellar Mossy Fibres
title_full Presynaptic Calcium Signalling in Cerebellar Mossy Fibres
title_fullStr Presynaptic Calcium Signalling in Cerebellar Mossy Fibres
title_full_unstemmed Presynaptic Calcium Signalling in Cerebellar Mossy Fibres
title_short Presynaptic Calcium Signalling in Cerebellar Mossy Fibres
title_sort presynaptic calcium signalling in cerebellar mossy fibres
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821199/
https://www.ncbi.nlm.nih.gov/pubmed/20162034
http://dx.doi.org/10.3389/neuro.04.001.2010
work_keys_str_mv AT thomsenlouizab presynapticcalciumsignallingincerebellarmossyfibres
AT jorntellhenrik presynapticcalciumsignallingincerebellarmossyfibres
AT midtgaardjens presynapticcalciumsignallingincerebellarmossyfibres