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Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments
The axon initial segment is an excitable membrane highly enriched in voltage-gated sodium channels that integrates neuronal inputs and initiates action potentials. This study identifies Na(v)1.6 as the voltage-gated sodium channel isoform at mature Purkinje neuron initial segments and reports an ess...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150881/ https://www.ncbi.nlm.nih.gov/pubmed/11724816 http://dx.doi.org/10.1083/jcb.200109026 |
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author | Jenkins, Scott M. Bennett, Vann |
author_facet | Jenkins, Scott M. Bennett, Vann |
author_sort | Jenkins, Scott M. |
collection | PubMed |
description | The axon initial segment is an excitable membrane highly enriched in voltage-gated sodium channels that integrates neuronal inputs and initiates action potentials. This study identifies Na(v)1.6 as the voltage-gated sodium channel isoform at mature Purkinje neuron initial segments and reports an essential role for ankyrin-G in coordinating the physiological assembly of Na(v)1.6, βIV spectrin, and the L1 cell adhesion molecules (L1 CAMs) neurofascin and NrCAM at initial segments of cerebellar Purkinje neurons. Ankyrin-G and βIV spectrin appear at axon initial segments by postnatal day 2, whereas L1 CAMs and Na(v)1.6 are not fully assembled at continuous high density along axon initial segments until postnatal day 9. L1 CAMs and Na(v)1.6 therefore do not initiate protein assembly at initial segments. βIV spectrin, Na(v)1.6, and L1 CAMs are not clustered in adult Purkinje neuron initial segments of mice lacking cerebellar ankyrin-G. These results support the conclusion that ankyrin-G coordinates the physiological assembly of a protein complex containing transmembrane adhesion molecules, voltage-gated sodium channels, and the spectrin membrane skeleton at axon initial segments. |
format | Text |
id | pubmed-2150881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21508812008-05-01 Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments Jenkins, Scott M. Bennett, Vann J Cell Biol Report The axon initial segment is an excitable membrane highly enriched in voltage-gated sodium channels that integrates neuronal inputs and initiates action potentials. This study identifies Na(v)1.6 as the voltage-gated sodium channel isoform at mature Purkinje neuron initial segments and reports an essential role for ankyrin-G in coordinating the physiological assembly of Na(v)1.6, βIV spectrin, and the L1 cell adhesion molecules (L1 CAMs) neurofascin and NrCAM at initial segments of cerebellar Purkinje neurons. Ankyrin-G and βIV spectrin appear at axon initial segments by postnatal day 2, whereas L1 CAMs and Na(v)1.6 are not fully assembled at continuous high density along axon initial segments until postnatal day 9. L1 CAMs and Na(v)1.6 therefore do not initiate protein assembly at initial segments. βIV spectrin, Na(v)1.6, and L1 CAMs are not clustered in adult Purkinje neuron initial segments of mice lacking cerebellar ankyrin-G. These results support the conclusion that ankyrin-G coordinates the physiological assembly of a protein complex containing transmembrane adhesion molecules, voltage-gated sodium channels, and the spectrin membrane skeleton at axon initial segments. The Rockefeller University Press 2001-11-26 /pmc/articles/PMC2150881/ /pubmed/11724816 http://dx.doi.org/10.1083/jcb.200109026 Text en Copyright © 2001, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Report Jenkins, Scott M. Bennett, Vann Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments |
title | Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments |
title_full | Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments |
title_fullStr | Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments |
title_full_unstemmed | Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments |
title_short | Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments |
title_sort | ankyrin-g coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and l1 cams at purkinje neuron initial segments |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150881/ https://www.ncbi.nlm.nih.gov/pubmed/11724816 http://dx.doi.org/10.1083/jcb.200109026 |
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