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The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons

The CRISPR-Cas13 system based on a bacterial enzyme has been explored as a powerful new method for RNA manipulation. Due to the high efficiency and specificity of RNA editing/interference achieved by this system, it is currently being developed as a new therapeutic tool for the treatment of neurolog...

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Detalles Bibliográficos
Autores principales: Wu, Qin-Wei, Kapfhammer, Josef P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067550/
https://www.ncbi.nlm.nih.gov/pubmed/33916905
http://dx.doi.org/10.3390/toxins13040262
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author Wu, Qin-Wei
Kapfhammer, Josef P.
author_facet Wu, Qin-Wei
Kapfhammer, Josef P.
author_sort Wu, Qin-Wei
collection PubMed
description The CRISPR-Cas13 system based on a bacterial enzyme has been explored as a powerful new method for RNA manipulation. Due to the high efficiency and specificity of RNA editing/interference achieved by this system, it is currently being developed as a new therapeutic tool for the treatment of neurological and other diseases. However, the safety of this new generation of RNA therapies is still unclear. In this study, we constructed a vector expressing CRISPR-Cas13 under a constitutive neuron-specific promoter. CRISPR-Cas13 from Leptotrichia wadei was expressed in primary cultures of mouse cortical neurons. We found that the presence of CRISPR-Cas13 impedes the development of cultured neurons. These results show a neurotoxic action of Cas13 and call for more studies to test for and possibly mitigate the toxic effects of Cas13 enzymes in order to improve CRISPR-Cas13-based tools for RNA targeting.
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spelling pubmed-80675502021-04-25 The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons Wu, Qin-Wei Kapfhammer, Josef P. Toxins (Basel) Communication The CRISPR-Cas13 system based on a bacterial enzyme has been explored as a powerful new method for RNA manipulation. Due to the high efficiency and specificity of RNA editing/interference achieved by this system, it is currently being developed as a new therapeutic tool for the treatment of neurological and other diseases. However, the safety of this new generation of RNA therapies is still unclear. In this study, we constructed a vector expressing CRISPR-Cas13 under a constitutive neuron-specific promoter. CRISPR-Cas13 from Leptotrichia wadei was expressed in primary cultures of mouse cortical neurons. We found that the presence of CRISPR-Cas13 impedes the development of cultured neurons. These results show a neurotoxic action of Cas13 and call for more studies to test for and possibly mitigate the toxic effects of Cas13 enzymes in order to improve CRISPR-Cas13-based tools for RNA targeting. MDPI 2021-04-07 /pmc/articles/PMC8067550/ /pubmed/33916905 http://dx.doi.org/10.3390/toxins13040262 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Wu, Qin-Wei
Kapfhammer, Josef P.
The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons
title The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons
title_full The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons
title_fullStr The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons
title_full_unstemmed The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons
title_short The Bacterial Enzyme Cas13 Interferes with Neurite Outgrowth from Cultured Cortical Neurons
title_sort bacterial enzyme cas13 interferes with neurite outgrowth from cultured cortical neurons
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067550/
https://www.ncbi.nlm.nih.gov/pubmed/33916905
http://dx.doi.org/10.3390/toxins13040262
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