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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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. |
format | Online Article Text |
id | pubmed-8851107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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