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mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells

Ca(2+) transients can be observed in the distal dendrites of Purkinje cells (PCs) despite their lack of action potential backpropagation. These Ca(2+) events in distal dendrites require specific patterns of PC firing, such as complex spikes (CS) or simple spikes (SS) of burst mode. Unlike CS, which...

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Autores principales: Jang, Dong Cheol, Ryu, Changhyeon, Chung, Geehoon, Kim, Sun Kwang, Kim, Sang Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175955/
https://www.ncbi.nlm.nih.gov/pubmed/37164648
http://dx.doi.org/10.5607/en22040
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author Jang, Dong Cheol
Ryu, Changhyeon
Chung, Geehoon
Kim, Sun Kwang
Kim, Sang Jeong
author_facet Jang, Dong Cheol
Ryu, Changhyeon
Chung, Geehoon
Kim, Sun Kwang
Kim, Sang Jeong
author_sort Jang, Dong Cheol
collection PubMed
description Ca(2+) transients can be observed in the distal dendrites of Purkinje cells (PCs) despite their lack of action potential backpropagation. These Ca(2+) events in distal dendrites require specific patterns of PC firing, such as complex spikes (CS) or simple spikes (SS) of burst mode. Unlike CS, which can act directly on voltage-gated calcium channels in the dendrites through climbing fiber inputs, the condition that can produce the Ca(2+) events in distal dendrites with burst mode SS is poorly understood. Here, we propose the interspike interval threshold (ISIT) for Ca(2+) transients in the distal dendrites of PC. We found that to induce the Ca(2+) transients in distal dendrites the frequency of spike firing of PC should reach 250 Hz (3 ms ISI). Metabotropic glutamate receptor 1 (mGluR1) activation significantly relieved the ISIT and established cellular conditions in which spike firing with 50 Hz (19 ms ISI) could induce Ca(2+) transients in the distal dendrites. In contrast, blocking T-type Ca(2+) channels or depleting the endoplasmic reticulum Ca(2+) store resulted in a stricter condition in which spike firing with 333 Hz (2 ms ISI) was required. Our findings demonstrate that the PC has strict ISIT for dendritic Ca(2+) transients, and this ISIT can be relieved by mGluR1 activation. This strict restriction of ISIT could contribute to the reduction of the signal-to-noise ratio in terms of collecting information by preventing excessive dendritic Ca(2+) transients through the spontaneous activity of PC.
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spelling pubmed-101759552023-05-13 mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells Jang, Dong Cheol Ryu, Changhyeon Chung, Geehoon Kim, Sun Kwang Kim, Sang Jeong Exp Neurobiol Short Communication Ca(2+) transients can be observed in the distal dendrites of Purkinje cells (PCs) despite their lack of action potential backpropagation. These Ca(2+) events in distal dendrites require specific patterns of PC firing, such as complex spikes (CS) or simple spikes (SS) of burst mode. Unlike CS, which can act directly on voltage-gated calcium channels in the dendrites through climbing fiber inputs, the condition that can produce the Ca(2+) events in distal dendrites with burst mode SS is poorly understood. Here, we propose the interspike interval threshold (ISIT) for Ca(2+) transients in the distal dendrites of PC. We found that to induce the Ca(2+) transients in distal dendrites the frequency of spike firing of PC should reach 250 Hz (3 ms ISI). Metabotropic glutamate receptor 1 (mGluR1) activation significantly relieved the ISIT and established cellular conditions in which spike firing with 50 Hz (19 ms ISI) could induce Ca(2+) transients in the distal dendrites. In contrast, blocking T-type Ca(2+) channels or depleting the endoplasmic reticulum Ca(2+) store resulted in a stricter condition in which spike firing with 333 Hz (2 ms ISI) was required. Our findings demonstrate that the PC has strict ISIT for dendritic Ca(2+) transients, and this ISIT can be relieved by mGluR1 activation. This strict restriction of ISIT could contribute to the reduction of the signal-to-noise ratio in terms of collecting information by preventing excessive dendritic Ca(2+) transients through the spontaneous activity of PC. The Korean Society for Brain and Neural Sciences 2023-04-30 2023-04-30 /pmc/articles/PMC10175955/ /pubmed/37164648 http://dx.doi.org/10.5607/en22040 Text en Copyright © Experimental Neurobiology 2023 https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Jang, Dong Cheol
Ryu, Changhyeon
Chung, Geehoon
Kim, Sun Kwang
Kim, Sang Jeong
mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells
title mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells
title_full mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells
title_fullStr mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells
title_full_unstemmed mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells
title_short mGluR1 Regulates the Interspike Interval Threshold for Dendritic Ca(2+) Transients in the Cerebellar Purkinje Cells
title_sort mglur1 regulates the interspike interval threshold for dendritic ca(2+) transients in the cerebellar purkinje cells
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175955/
https://www.ncbi.nlm.nih.gov/pubmed/37164648
http://dx.doi.org/10.5607/en22040
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