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Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity

Mechanical forces are increasingly recognized as major regulators of several physiological processes at both the molecular and cellular level; therefore, a deep understanding of the sensing of these forces and their conversion into electrical signals are essential for studying the mechanosensitive p...

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Autores principales: Marrese, Marica, Lonardoni, Davide, Boi, Fabio, van Hoorn, Hedde, Maccione, Alessandro, Zordan, Stefano, Iannuzzi, Davide, Berdondini, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776634/
https://www.ncbi.nlm.nih.gov/pubmed/31611765
http://dx.doi.org/10.3389/fnins.2019.01023
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author Marrese, Marica
Lonardoni, Davide
Boi, Fabio
van Hoorn, Hedde
Maccione, Alessandro
Zordan, Stefano
Iannuzzi, Davide
Berdondini, Luca
author_facet Marrese, Marica
Lonardoni, Davide
Boi, Fabio
van Hoorn, Hedde
Maccione, Alessandro
Zordan, Stefano
Iannuzzi, Davide
Berdondini, Luca
author_sort Marrese, Marica
collection PubMed
description Mechanical forces are increasingly recognized as major regulators of several physiological processes at both the molecular and cellular level; therefore, a deep understanding of the sensing of these forces and their conversion into electrical signals are essential for studying the mechanosensitive properties of soft biological tissues. To contribute to this field, we present a dual-purpose device able to mechanically stimulate retinal tissue and to record the spiking activity of retinal ganglion cells (RGCs). This new instrument relies on combining ferrule-top micro-indentation, which provides local measurements of viscoelasticity, with high-density multi-electrode array (HD-MEAs) to simultaneously record the spontaneous activity of the retina. In this paper, we introduce this instrument, describe its technical characteristics, and present a proof-of-concept experiment that shows how RGC spiking activity of explanted mice retinas respond to mechanical micro-stimulations of their photoreceptor layer. The data suggest that, under specific conditions of indentation, the retina perceive the mechanical stimulation as modulation of the visual input, besides the longer time-scale of activation, and the increase in spiking activity is not only localized under the indentation probe, but it propagates across the retinal tissue.
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spelling pubmed-67766342019-10-14 Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity Marrese, Marica Lonardoni, Davide Boi, Fabio van Hoorn, Hedde Maccione, Alessandro Zordan, Stefano Iannuzzi, Davide Berdondini, Luca Front Neurosci Neuroscience Mechanical forces are increasingly recognized as major regulators of several physiological processes at both the molecular and cellular level; therefore, a deep understanding of the sensing of these forces and their conversion into electrical signals are essential for studying the mechanosensitive properties of soft biological tissues. To contribute to this field, we present a dual-purpose device able to mechanically stimulate retinal tissue and to record the spiking activity of retinal ganglion cells (RGCs). This new instrument relies on combining ferrule-top micro-indentation, which provides local measurements of viscoelasticity, with high-density multi-electrode array (HD-MEAs) to simultaneously record the spontaneous activity of the retina. In this paper, we introduce this instrument, describe its technical characteristics, and present a proof-of-concept experiment that shows how RGC spiking activity of explanted mice retinas respond to mechanical micro-stimulations of their photoreceptor layer. The data suggest that, under specific conditions of indentation, the retina perceive the mechanical stimulation as modulation of the visual input, besides the longer time-scale of activation, and the increase in spiking activity is not only localized under the indentation probe, but it propagates across the retinal tissue. Frontiers Media S.A. 2019-09-27 /pmc/articles/PMC6776634/ /pubmed/31611765 http://dx.doi.org/10.3389/fnins.2019.01023 Text en Copyright © 2019 Marrese, Lonardoni, Boi, van Hoorn, Maccione, Zordan, Iannuzzi and Berdondini. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Marrese, Marica
Lonardoni, Davide
Boi, Fabio
van Hoorn, Hedde
Maccione, Alessandro
Zordan, Stefano
Iannuzzi, Davide
Berdondini, Luca
Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity
title Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity
title_full Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity
title_fullStr Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity
title_full_unstemmed Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity
title_short Investigating the Effects of Mechanical Stimulation on Retinal Ganglion Cell Spontaneous Spiking Activity
title_sort investigating the effects of mechanical stimulation on retinal ganglion cell spontaneous spiking activity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776634/
https://www.ncbi.nlm.nih.gov/pubmed/31611765
http://dx.doi.org/10.3389/fnins.2019.01023
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