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The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons
Certain neuron types fire spontaneously at high rates, an ability that is crucial for their function in brain circuits. The spontaneously active GABAergic neurons of the substantia nigra pars reticulata (SNr), a major output of the basal ganglia, provide tonic inhibition of downstream brain areas. A...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902561/ https://www.ncbi.nlm.nih.gov/pubmed/27177420 http://dx.doi.org/10.7554/eLife.15271 |
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author | Lutas, Andrew Lahmann, Carolina Soumillon, Magali Yellen, Gary |
author_facet | Lutas, Andrew Lahmann, Carolina Soumillon, Magali Yellen, Gary |
author_sort | Lutas, Andrew |
collection | PubMed |
description | Certain neuron types fire spontaneously at high rates, an ability that is crucial for their function in brain circuits. The spontaneously active GABAergic neurons of the substantia nigra pars reticulata (SNr), a major output of the basal ganglia, provide tonic inhibition of downstream brain areas. A depolarizing 'leak' current supports this firing pattern, but its molecular basis remains poorly understood. To understand how SNr neurons maintain tonic activity, we used single-cell RNA sequencing to determine the transcriptome of individual mouse SNr neurons. We discovered that SNr neurons express the sodium leak channel, NALCN, and that SNr neurons lacking NALCN have impaired spontaneous firing. In addition, NALCN is involved in the modulation of excitability by changes in glycolysis and by activation of muscarinic acetylcholine receptors. Our findings suggest that disruption of NALCN could impair the basal ganglia circuit, which may underlie the severe motor deficits in humans carrying mutations in NALCN. DOI: http://dx.doi.org/10.7554/eLife.15271.001 |
format | Online Article Text |
id | pubmed-4902561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49025612016-06-13 The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons Lutas, Andrew Lahmann, Carolina Soumillon, Magali Yellen, Gary eLife Neuroscience Certain neuron types fire spontaneously at high rates, an ability that is crucial for their function in brain circuits. The spontaneously active GABAergic neurons of the substantia nigra pars reticulata (SNr), a major output of the basal ganglia, provide tonic inhibition of downstream brain areas. A depolarizing 'leak' current supports this firing pattern, but its molecular basis remains poorly understood. To understand how SNr neurons maintain tonic activity, we used single-cell RNA sequencing to determine the transcriptome of individual mouse SNr neurons. We discovered that SNr neurons express the sodium leak channel, NALCN, and that SNr neurons lacking NALCN have impaired spontaneous firing. In addition, NALCN is involved in the modulation of excitability by changes in glycolysis and by activation of muscarinic acetylcholine receptors. Our findings suggest that disruption of NALCN could impair the basal ganglia circuit, which may underlie the severe motor deficits in humans carrying mutations in NALCN. DOI: http://dx.doi.org/10.7554/eLife.15271.001 eLife Sciences Publications, Ltd 2016-05-13 /pmc/articles/PMC4902561/ /pubmed/27177420 http://dx.doi.org/10.7554/eLife.15271 Text en © 2016, Lutas et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Lutas, Andrew Lahmann, Carolina Soumillon, Magali Yellen, Gary The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons |
title | The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons |
title_full | The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons |
title_fullStr | The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons |
title_full_unstemmed | The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons |
title_short | The leak channel NALCN controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons |
title_sort | leak channel nalcn controls tonic firing and glycolytic sensitivity of substantia nigra pars reticulata neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902561/ https://www.ncbi.nlm.nih.gov/pubmed/27177420 http://dx.doi.org/10.7554/eLife.15271 |
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