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Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces

There is growing evidence suggesting that mechanical properties of CNS neurons may play an important regulatory role in cellular processes. Here, we employ an oscillatory optical tweezers (OOT) to exert a local indentation with forces in the range of 5–50 pN. We found that single local indentation a...

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Detalles Bibliográficos
Autores principales: Falleroni, Fabio, Bocchero, Ulisse, Mortal, Simone, Li, Yunzhen, Ye, Zhongjie, Cojoc, Dan, Torre, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851107/
https://www.ncbi.nlm.nih.gov/pubmed/35198872
http://dx.doi.org/10.1016/j.isci.2022.103807
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author Falleroni, Fabio
Bocchero, Ulisse
Mortal, Simone
Li, Yunzhen
Ye, Zhongjie
Cojoc, Dan
Torre, Vincent
author_facet Falleroni, Fabio
Bocchero, Ulisse
Mortal, Simone
Li, Yunzhen
Ye, Zhongjie
Cojoc, Dan
Torre, Vincent
author_sort Falleroni, Fabio
collection PubMed
description There is growing evidence suggesting that mechanical properties of CNS neurons may play an important regulatory role in cellular processes. Here, we employ an oscillatory optical tweezers (OOT) to exert a local indentation with forces in the range of 5–50 pN. We found that single local indentation above a threshold of 13 ± 1 pN evokes a transient intracellular calcium change, whereas repeated mechanical stimulations induce a more sustained and variable calcium response. Importantly, neurons were able to differentiate the magnitude of mechanical stimuli. Chemical perturbation and whole-cell patch clamp recordings suggest that mechanically evoked response requires the influx of extracellular calcium through transmembrane ion channels. Moreover, we observed a mechanically evoked activation of the CAMKII and small G protein RhoA. These results all together suggest that mechanical signaling among developed neurons fully operates in neuronal networks under physiological conditions.
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spelling pubmed-88511072022-02-22 Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces Falleroni, Fabio Bocchero, Ulisse Mortal, Simone Li, Yunzhen Ye, Zhongjie Cojoc, Dan Torre, Vincent iScience Article There is growing evidence suggesting that mechanical properties of CNS neurons may play an important regulatory role in cellular processes. Here, we employ an oscillatory optical tweezers (OOT) to exert a local indentation with forces in the range of 5–50 pN. We found that single local indentation above a threshold of 13 ± 1 pN evokes a transient intracellular calcium change, whereas repeated mechanical stimulations induce a more sustained and variable calcium response. Importantly, neurons were able to differentiate the magnitude of mechanical stimuli. Chemical perturbation and whole-cell patch clamp recordings suggest that mechanically evoked response requires the influx of extracellular calcium through transmembrane ion channels. Moreover, we observed a mechanically evoked activation of the CAMKII and small G protein RhoA. These results all together suggest that mechanical signaling among developed neurons fully operates in neuronal networks under physiological conditions. Elsevier 2022-01-25 /pmc/articles/PMC8851107/ /pubmed/35198872 http://dx.doi.org/10.1016/j.isci.2022.103807 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Falleroni, Fabio
Bocchero, Ulisse
Mortal, Simone
Li, Yunzhen
Ye, Zhongjie
Cojoc, Dan
Torre, Vincent
Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces
title Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces
title_full Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces
title_fullStr Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces
title_full_unstemmed Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces
title_short Mechanotransduction in hippocampal neurons operates under localized low picoNewton forces
title_sort mechanotransduction in hippocampal neurons operates under localized low piconewton forces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851107/
https://www.ncbi.nlm.nih.gov/pubmed/35198872
http://dx.doi.org/10.1016/j.isci.2022.103807
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