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SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123

Chloride homeostasis determines the impact of inhibitory synaptic transmission and thereby mediates the excitability of neurons. Even though cerebellar Purkinje cells (PCs) receive a pronounced inhibitory GABAergic input from stellate and basket cells, the role of chloride homeostasis in these neuro...

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Autores principales: Rahmati, Negah, Vinueza Veloz, Maria Fernanda, Xu, Jie, Barone, Sharon, Rodolfo Ben Hamida, Nahuel, Schonewille, Martijn, Hoebeek, Freek E., Soleimani, Manoocher, De Zeeuw, Chris I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908300/
https://www.ncbi.nlm.nih.gov/pubmed/27390771
http://dx.doi.org/10.1523/ENEURO.0028-16.2016
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author Rahmati, Negah
Vinueza Veloz, Maria Fernanda
Xu, Jie
Barone, Sharon
Rodolfo Ben Hamida, Nahuel
Schonewille, Martijn
Hoebeek, Freek E.
Soleimani, Manoocher
De Zeeuw, Chris I.
author_facet Rahmati, Negah
Vinueza Veloz, Maria Fernanda
Xu, Jie
Barone, Sharon
Rodolfo Ben Hamida, Nahuel
Schonewille, Martijn
Hoebeek, Freek E.
Soleimani, Manoocher
De Zeeuw, Chris I.
author_sort Rahmati, Negah
collection PubMed
description Chloride homeostasis determines the impact of inhibitory synaptic transmission and thereby mediates the excitability of neurons. Even though cerebellar Purkinje cells (PCs) receive a pronounced inhibitory GABAergic input from stellate and basket cells, the role of chloride homeostasis in these neurons is largely unknown. Here we studied at both the cellular and systems physiological level the function of a recently discovered chloride channel, SLC26A11 or kidney brain anion transporter (KBAT), which is prominently expressed in PCs. Using perforated patch clamp recordings of PCs, we found that a lack of KBAT channel in PC-specific KBAT KO mice (L7-KBAT KOs) induces a negative shift in the reversal potential of chloride as reflected in the GABA(A)-receptor-evoked currents, indicating a decrease in intracellular chloride concentration. Surprisingly, both in vitro and in vivo PCs in L7-KBAT KOs showed a significantly increased action potential firing frequency of simple spikes, which correlated with impaired motor performance on the Erasmus Ladder. Our findings support an important role for SLC26A11 in moderating chloride homeostasis and neuronal activity in the cerebellum.
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spelling pubmed-49083002016-07-07 SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123 Rahmati, Negah Vinueza Veloz, Maria Fernanda Xu, Jie Barone, Sharon Rodolfo Ben Hamida, Nahuel Schonewille, Martijn Hoebeek, Freek E. Soleimani, Manoocher De Zeeuw, Chris I. eNeuro New Research Chloride homeostasis determines the impact of inhibitory synaptic transmission and thereby mediates the excitability of neurons. Even though cerebellar Purkinje cells (PCs) receive a pronounced inhibitory GABAergic input from stellate and basket cells, the role of chloride homeostasis in these neurons is largely unknown. Here we studied at both the cellular and systems physiological level the function of a recently discovered chloride channel, SLC26A11 or kidney brain anion transporter (KBAT), which is prominently expressed in PCs. Using perforated patch clamp recordings of PCs, we found that a lack of KBAT channel in PC-specific KBAT KO mice (L7-KBAT KOs) induces a negative shift in the reversal potential of chloride as reflected in the GABA(A)-receptor-evoked currents, indicating a decrease in intracellular chloride concentration. Surprisingly, both in vitro and in vivo PCs in L7-KBAT KOs showed a significantly increased action potential firing frequency of simple spikes, which correlated with impaired motor performance on the Erasmus Ladder. Our findings support an important role for SLC26A11 in moderating chloride homeostasis and neuronal activity in the cerebellum. Society for Neuroscience 2016-06-15 /pmc/articles/PMC4908300/ /pubmed/27390771 http://dx.doi.org/10.1523/ENEURO.0028-16.2016 Text en Copyright © 2016 Rahmati et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Rahmati, Negah
Vinueza Veloz, Maria Fernanda
Xu, Jie
Barone, Sharon
Rodolfo Ben Hamida, Nahuel
Schonewille, Martijn
Hoebeek, Freek E.
Soleimani, Manoocher
De Zeeuw, Chris I.
SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123
title SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123
title_full SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123
title_fullStr SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123
title_full_unstemmed SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123
title_short SLC26A11 (KBAT) in Purkinje Cells Is Critical for Inhibitory Transmission and Contributes to Locomotor Coordination123
title_sort slc26a11 (kbat) in purkinje cells is critical for inhibitory transmission and contributes to locomotor coordination123
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908300/
https://www.ncbi.nlm.nih.gov/pubmed/27390771
http://dx.doi.org/10.1523/ENEURO.0028-16.2016
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