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Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy
Brain tumor patients commonly present with epileptic seizures. We show that tumor-associated seizures are the consequence of impaired GABAergic inhibition due to an overall loss of peritumoral fast spiking interneurons (FSNs) concomitant with a significantly reduced firing rate of those that remain....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226462/ https://www.ncbi.nlm.nih.gov/pubmed/30413686 http://dx.doi.org/10.1038/s41467-018-07113-0 |
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author | Tewari, Bhanu P. Chaunsali, Lata Campbell, Susan L. Patel, Dipan C. Goode, Adam E. Sontheimer, Harald |
author_facet | Tewari, Bhanu P. Chaunsali, Lata Campbell, Susan L. Patel, Dipan C. Goode, Adam E. Sontheimer, Harald |
author_sort | Tewari, Bhanu P. |
collection | PubMed |
description | Brain tumor patients commonly present with epileptic seizures. We show that tumor-associated seizures are the consequence of impaired GABAergic inhibition due to an overall loss of peritumoral fast spiking interneurons (FSNs) concomitant with a significantly reduced firing rate of those that remain. The reduced firing is due to the degradation of perineuronal nets (PNNs) that surround FSNs. We show that PNNs decrease specific membrane capacitance of FSNs permitting them to fire action potentials at supra-physiological frequencies. Tumor-released proteolytic enzymes degrade PNNs, resulting in increased membrane capacitance, reduced firing, and hence decreased GABA release. These studies uncovered a hitherto unknown role of PNNs as an electrostatic insulator that reduces specific membrane capacitance, functionally akin to myelin sheaths around axons, thereby permitting FSNs to exceed physiological firing rates. Disruption of PNNs may similarly account for excitation-inhibition imbalances in other forms of epilepsy and PNN protection through proteolytic inhibition may provide therapeutic benefits. |
format | Online Article Text |
id | pubmed-6226462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62264622018-11-13 Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy Tewari, Bhanu P. Chaunsali, Lata Campbell, Susan L. Patel, Dipan C. Goode, Adam E. Sontheimer, Harald Nat Commun Article Brain tumor patients commonly present with epileptic seizures. We show that tumor-associated seizures are the consequence of impaired GABAergic inhibition due to an overall loss of peritumoral fast spiking interneurons (FSNs) concomitant with a significantly reduced firing rate of those that remain. The reduced firing is due to the degradation of perineuronal nets (PNNs) that surround FSNs. We show that PNNs decrease specific membrane capacitance of FSNs permitting them to fire action potentials at supra-physiological frequencies. Tumor-released proteolytic enzymes degrade PNNs, resulting in increased membrane capacitance, reduced firing, and hence decreased GABA release. These studies uncovered a hitherto unknown role of PNNs as an electrostatic insulator that reduces specific membrane capacitance, functionally akin to myelin sheaths around axons, thereby permitting FSNs to exceed physiological firing rates. Disruption of PNNs may similarly account for excitation-inhibition imbalances in other forms of epilepsy and PNN protection through proteolytic inhibition may provide therapeutic benefits. Nature Publishing Group UK 2018-11-09 /pmc/articles/PMC6226462/ /pubmed/30413686 http://dx.doi.org/10.1038/s41467-018-07113-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tewari, Bhanu P. Chaunsali, Lata Campbell, Susan L. Patel, Dipan C. Goode, Adam E. Sontheimer, Harald Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy |
title | Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy |
title_full | Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy |
title_fullStr | Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy |
title_full_unstemmed | Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy |
title_short | Perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy |
title_sort | perineuronal nets decrease membrane capacitance of peritumoral fast spiking interneurons in a model of epilepsy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226462/ https://www.ncbi.nlm.nih.gov/pubmed/30413686 http://dx.doi.org/10.1038/s41467-018-07113-0 |
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