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Optogenetically induced cellular habituation in non-neuronal cells

Habituation, defined as the reversible decrement of a response during repetitive stimulation, is widely established as a form of non-associative learning. Though more commonly ascribed to neural cells and systems, habituation has also been observed in single aneural cells, although evidence is limit...

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Autores principales: Bonzanni, Mattia, Rouleau, Nicolas, Levin, Michael, Kaplan, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968872/
https://www.ncbi.nlm.nih.gov/pubmed/31951626
http://dx.doi.org/10.1371/journal.pone.0227230
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author Bonzanni, Mattia
Rouleau, Nicolas
Levin, Michael
Kaplan, David L.
author_facet Bonzanni, Mattia
Rouleau, Nicolas
Levin, Michael
Kaplan, David L.
author_sort Bonzanni, Mattia
collection PubMed
description Habituation, defined as the reversible decrement of a response during repetitive stimulation, is widely established as a form of non-associative learning. Though more commonly ascribed to neural cells and systems, habituation has also been observed in single aneural cells, although evidence is limited. Considering the generalizability of the habituation process, we tested the degree to which organism-level behavioral and single cell manifestations were similar. Human embryonic kidney (HEK) cells that overexpressed an optogenetic actuator were photostimulated to test the effect of different stimulation protocols on cell responses. Depolarization induced by the photocurrent decreased successively over the stimulation protocol and the effect was reversible upon withdrawal of the stimulus. In addition to frequency- and intensity-dependent effects, the history of stimulations on the cells impacted subsequent depolarization in response to further stimulation. We identified tetraethylammonium (TEA)-sensitive native K(+) channels as one of the mediators of this habituation phenotype. Finally, we used a theoretical model of habituation to elucidate some mechanistic aspects of the habituation response. In conclusion, we affirm that habituation is a time- and state-dependent biological strategy that can be adopted also by individual non-neuronal cells in response to repetitive stimuli.
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spelling pubmed-69688722020-01-26 Optogenetically induced cellular habituation in non-neuronal cells Bonzanni, Mattia Rouleau, Nicolas Levin, Michael Kaplan, David L. PLoS One Research Article Habituation, defined as the reversible decrement of a response during repetitive stimulation, is widely established as a form of non-associative learning. Though more commonly ascribed to neural cells and systems, habituation has also been observed in single aneural cells, although evidence is limited. Considering the generalizability of the habituation process, we tested the degree to which organism-level behavioral and single cell manifestations were similar. Human embryonic kidney (HEK) cells that overexpressed an optogenetic actuator were photostimulated to test the effect of different stimulation protocols on cell responses. Depolarization induced by the photocurrent decreased successively over the stimulation protocol and the effect was reversible upon withdrawal of the stimulus. In addition to frequency- and intensity-dependent effects, the history of stimulations on the cells impacted subsequent depolarization in response to further stimulation. We identified tetraethylammonium (TEA)-sensitive native K(+) channels as one of the mediators of this habituation phenotype. Finally, we used a theoretical model of habituation to elucidate some mechanistic aspects of the habituation response. In conclusion, we affirm that habituation is a time- and state-dependent biological strategy that can be adopted also by individual non-neuronal cells in response to repetitive stimuli. Public Library of Science 2020-01-17 /pmc/articles/PMC6968872/ /pubmed/31951626 http://dx.doi.org/10.1371/journal.pone.0227230 Text en © 2020 Bonzanni et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bonzanni, Mattia
Rouleau, Nicolas
Levin, Michael
Kaplan, David L.
Optogenetically induced cellular habituation in non-neuronal cells
title Optogenetically induced cellular habituation in non-neuronal cells
title_full Optogenetically induced cellular habituation in non-neuronal cells
title_fullStr Optogenetically induced cellular habituation in non-neuronal cells
title_full_unstemmed Optogenetically induced cellular habituation in non-neuronal cells
title_short Optogenetically induced cellular habituation in non-neuronal cells
title_sort optogenetically induced cellular habituation in non-neuronal cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968872/
https://www.ncbi.nlm.nih.gov/pubmed/31951626
http://dx.doi.org/10.1371/journal.pone.0227230
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