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On-demand cell-autonomous gene therapy for brain circuit disorders
Several neurodevelopmental and neuropsychiatric disorders are characterized by intermittent episodes of pathological activity. Although genetic therapies offer the ability to modulate neuronal excitability, a limiting factor is that they do not discriminate between neurons involved in circuit pathol...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613996/ https://www.ncbi.nlm.nih.gov/pubmed/36378958 http://dx.doi.org/10.1126/science.abq6656 |
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author | Qiu, Yichen O’Neill, Nathanael Maffei, Benito Zourray, Clara Almacellas-Barbanoj, Amanda Carpenter, Jenna C. Jones, Steffan P. Leite, Marco Turner, Thomas J. Moreira, Francisco C. Snowball, Albert Shekh-Ahmad, Tawfeeq Magloire, Vincent Barral, Serena Kurian, Manju A. Walker, Matthew C. Schorge, Stephanie Kullmann, Dimitri M. Lignani, Gabriele |
author_facet | Qiu, Yichen O’Neill, Nathanael Maffei, Benito Zourray, Clara Almacellas-Barbanoj, Amanda Carpenter, Jenna C. Jones, Steffan P. Leite, Marco Turner, Thomas J. Moreira, Francisco C. Snowball, Albert Shekh-Ahmad, Tawfeeq Magloire, Vincent Barral, Serena Kurian, Manju A. Walker, Matthew C. Schorge, Stephanie Kullmann, Dimitri M. Lignani, Gabriele |
author_sort | Qiu, Yichen |
collection | PubMed |
description | Several neurodevelopmental and neuropsychiatric disorders are characterized by intermittent episodes of pathological activity. Although genetic therapies offer the ability to modulate neuronal excitability, a limiting factor is that they do not discriminate between neurons involved in circuit pathologies and “healthy” surrounding or intermingled neurons. We describe a gene therapy strategy that down-regulates the excitability of overactive neurons in closed loop, which we tested in models of epilepsy. We used an immediate early gene promoter to drive the expression of Kv1.1 potassium channels specifically in hyperactive neurons, and only for as long as they exhibit abnormal activity. Neuronal excitability was reduced by seizure-related activity, leading to a persistent antiepileptic effect without interfering with normal behaviors. Activity-dependent gene therapy is a promising on- demand cell-autonomous treatment for brain circuit disorders. |
format | Online Article Text |
id | pubmed-7613996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76139962022-12-28 On-demand cell-autonomous gene therapy for brain circuit disorders Qiu, Yichen O’Neill, Nathanael Maffei, Benito Zourray, Clara Almacellas-Barbanoj, Amanda Carpenter, Jenna C. Jones, Steffan P. Leite, Marco Turner, Thomas J. Moreira, Francisco C. Snowball, Albert Shekh-Ahmad, Tawfeeq Magloire, Vincent Barral, Serena Kurian, Manju A. Walker, Matthew C. Schorge, Stephanie Kullmann, Dimitri M. Lignani, Gabriele Science Article Several neurodevelopmental and neuropsychiatric disorders are characterized by intermittent episodes of pathological activity. Although genetic therapies offer the ability to modulate neuronal excitability, a limiting factor is that they do not discriminate between neurons involved in circuit pathologies and “healthy” surrounding or intermingled neurons. We describe a gene therapy strategy that down-regulates the excitability of overactive neurons in closed loop, which we tested in models of epilepsy. We used an immediate early gene promoter to drive the expression of Kv1.1 potassium channels specifically in hyperactive neurons, and only for as long as they exhibit abnormal activity. Neuronal excitability was reduced by seizure-related activity, leading to a persistent antiepileptic effect without interfering with normal behaviors. Activity-dependent gene therapy is a promising on- demand cell-autonomous treatment for brain circuit disorders. 2022-11-04 2022-11-03 /pmc/articles/PMC7613996/ /pubmed/36378958 http://dx.doi.org/10.1126/science.abq6656 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license. |
spellingShingle | Article Qiu, Yichen O’Neill, Nathanael Maffei, Benito Zourray, Clara Almacellas-Barbanoj, Amanda Carpenter, Jenna C. Jones, Steffan P. Leite, Marco Turner, Thomas J. Moreira, Francisco C. Snowball, Albert Shekh-Ahmad, Tawfeeq Magloire, Vincent Barral, Serena Kurian, Manju A. Walker, Matthew C. Schorge, Stephanie Kullmann, Dimitri M. Lignani, Gabriele On-demand cell-autonomous gene therapy for brain circuit disorders |
title | On-demand cell-autonomous gene therapy for brain circuit disorders |
title_full | On-demand cell-autonomous gene therapy for brain circuit disorders |
title_fullStr | On-demand cell-autonomous gene therapy for brain circuit disorders |
title_full_unstemmed | On-demand cell-autonomous gene therapy for brain circuit disorders |
title_short | On-demand cell-autonomous gene therapy for brain circuit disorders |
title_sort | on-demand cell-autonomous gene therapy for brain circuit disorders |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613996/ https://www.ncbi.nlm.nih.gov/pubmed/36378958 http://dx.doi.org/10.1126/science.abq6656 |
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