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A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences
Astrocytes, one of the most prevalent cell types in the central nervous system (CNS), are critically involved in neural function. Genetically manipulating astrocytes is an essential tool in understanding and affecting their roles. Adeno-associated viruses (AAVs) enable rapid genetic manipulation; ho...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654773/ https://www.ncbi.nlm.nih.gov/pubmed/37973910 http://dx.doi.org/10.1038/s41467-023-42746-w |
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author | Gleichman, Amy J. Kawaguchi, Riki Sofroniew, Michael V. Carmichael, S. Thomas |
author_facet | Gleichman, Amy J. Kawaguchi, Riki Sofroniew, Michael V. Carmichael, S. Thomas |
author_sort | Gleichman, Amy J. |
collection | PubMed |
description | Astrocytes, one of the most prevalent cell types in the central nervous system (CNS), are critically involved in neural function. Genetically manipulating astrocytes is an essential tool in understanding and affecting their roles. Adeno-associated viruses (AAVs) enable rapid genetic manipulation; however, astrocyte specificity of AAVs can be limited, with high off-target expression in neurons and sparsely in endothelial cells. Here, we report the development of a cassette of four copies of six miRNA targeting sequences (4x6T) which triggers transgene degradation specifically in neurons and endothelial cells. In combination with the GfaABC1D promoter, 4x6T increases astrocytic specificity of Cre with a viral reporter from <50% to >99% in multiple serotypes in mice, and confers astrocyte specificity in multiple recombinases and reporters. We also present empty vectors to add 4x6T to other cargo, independently and in Cre/Dre-dependent forms. This toolbox of AAVs allows rapid manipulation of astrocytes throughout the CNS, is compatible with different AAV serotypes, and demonstrates the efficacy of using multiplexed miRNA targeting sequences to decrease expression in multiple off-target cell populations simultaneously. |
format | Online Article Text |
id | pubmed-10654773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106547732023-11-16 A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences Gleichman, Amy J. Kawaguchi, Riki Sofroniew, Michael V. Carmichael, S. Thomas Nat Commun Article Astrocytes, one of the most prevalent cell types in the central nervous system (CNS), are critically involved in neural function. Genetically manipulating astrocytes is an essential tool in understanding and affecting their roles. Adeno-associated viruses (AAVs) enable rapid genetic manipulation; however, astrocyte specificity of AAVs can be limited, with high off-target expression in neurons and sparsely in endothelial cells. Here, we report the development of a cassette of four copies of six miRNA targeting sequences (4x6T) which triggers transgene degradation specifically in neurons and endothelial cells. In combination with the GfaABC1D promoter, 4x6T increases astrocytic specificity of Cre with a viral reporter from <50% to >99% in multiple serotypes in mice, and confers astrocyte specificity in multiple recombinases and reporters. We also present empty vectors to add 4x6T to other cargo, independently and in Cre/Dre-dependent forms. This toolbox of AAVs allows rapid manipulation of astrocytes throughout the CNS, is compatible with different AAV serotypes, and demonstrates the efficacy of using multiplexed miRNA targeting sequences to decrease expression in multiple off-target cell populations simultaneously. Nature Publishing Group UK 2023-11-16 /pmc/articles/PMC10654773/ /pubmed/37973910 http://dx.doi.org/10.1038/s41467-023-42746-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gleichman, Amy J. Kawaguchi, Riki Sofroniew, Michael V. Carmichael, S. Thomas A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences |
title | A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences |
title_full | A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences |
title_fullStr | A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences |
title_full_unstemmed | A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences |
title_short | A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences |
title_sort | toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microrna targeting sequences |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654773/ https://www.ncbi.nlm.nih.gov/pubmed/37973910 http://dx.doi.org/10.1038/s41467-023-42746-w |
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