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Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel
Development of remote stimulation techniques for neuronal tissues represents a challenging goal. Among the potential methods, mechanical stimuli are the most promising vectors to convey information non-invasively into intact brain tissue. In this context, selective mechano-sensitization of neuronal...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897719/ https://www.ncbi.nlm.nih.gov/pubmed/29361543 http://dx.doi.org/10.1242/jcs.210393 |
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author | Soloperto, Alessandro Boccaccio, Anna Contestabile, Andrea Moroni, Monica Hallinan, Grace I. Palazzolo, Gemma Chad, John Deinhardt, Katrin Carugo, Dario Difato, Francesco |
author_facet | Soloperto, Alessandro Boccaccio, Anna Contestabile, Andrea Moroni, Monica Hallinan, Grace I. Palazzolo, Gemma Chad, John Deinhardt, Katrin Carugo, Dario Difato, Francesco |
author_sort | Soloperto, Alessandro |
collection | PubMed |
description | Development of remote stimulation techniques for neuronal tissues represents a challenging goal. Among the potential methods, mechanical stimuli are the most promising vectors to convey information non-invasively into intact brain tissue. In this context, selective mechano-sensitization of neuronal circuits would pave the way to develop a new cell-type-specific stimulation approach. We report here, for the first time, the development and characterization of mechano-sensitized neuronal networks through the heterologous expression of an engineered bacterial large-conductance mechanosensitive ion channel (MscL). The neuronal functional expression of the MscL was validated through patch-clamp recordings upon application of calibrated suction pressures. Moreover, we verified the effective development of in-vitro neuronal networks expressing the engineered MscL in terms of cell survival, number of synaptic puncta and spontaneous network activity. The pure mechanosensitivity of the engineered MscL, with its wide genetic modification library, may represent a versatile tool to further develop a mechano-genetic approach. This article has an associated First Person interview with the first author of the paper. |
format | Online Article Text |
id | pubmed-5897719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-58977192018-04-25 Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel Soloperto, Alessandro Boccaccio, Anna Contestabile, Andrea Moroni, Monica Hallinan, Grace I. Palazzolo, Gemma Chad, John Deinhardt, Katrin Carugo, Dario Difato, Francesco J Cell Sci Research Article Development of remote stimulation techniques for neuronal tissues represents a challenging goal. Among the potential methods, mechanical stimuli are the most promising vectors to convey information non-invasively into intact brain tissue. In this context, selective mechano-sensitization of neuronal circuits would pave the way to develop a new cell-type-specific stimulation approach. We report here, for the first time, the development and characterization of mechano-sensitized neuronal networks through the heterologous expression of an engineered bacterial large-conductance mechanosensitive ion channel (MscL). The neuronal functional expression of the MscL was validated through patch-clamp recordings upon application of calibrated suction pressures. Moreover, we verified the effective development of in-vitro neuronal networks expressing the engineered MscL in terms of cell survival, number of synaptic puncta and spontaneous network activity. The pure mechanosensitivity of the engineered MscL, with its wide genetic modification library, may represent a versatile tool to further develop a mechano-genetic approach. This article has an associated First Person interview with the first author of the paper. The Company of Biologists Ltd 2018-03-01 /pmc/articles/PMC5897719/ /pubmed/29361543 http://dx.doi.org/10.1242/jcs.210393 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Soloperto, Alessandro Boccaccio, Anna Contestabile, Andrea Moroni, Monica Hallinan, Grace I. Palazzolo, Gemma Chad, John Deinhardt, Katrin Carugo, Dario Difato, Francesco Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel |
title | Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel |
title_full | Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel |
title_fullStr | Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel |
title_full_unstemmed | Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel |
title_short | Mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel |
title_sort | mechano-sensitization of mammalian neuronal networks through expression of the bacterial large-conductance mechanosensitive ion channel |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897719/ https://www.ncbi.nlm.nih.gov/pubmed/29361543 http://dx.doi.org/10.1242/jcs.210393 |
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