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All-optical observation on activity-dependent nanoscale dynamics of myelinated axons

SIGNIFICANCE: In the mammalian brain, rapid conduction of neural information is supported by the myelin, the functional efficacy of which shows steep dependence on its nanoscale cytoarchitecture. Although previous in vitro studies have suggested that neural activity accompanies nanometer-scale cellu...

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Autores principales: Kwon, Junhwan, Lee, Sungho, Jo, Yongjae, Choi, Myunghwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868287/
https://www.ncbi.nlm.nih.gov/pubmed/36699624
http://dx.doi.org/10.1117/1.NPh.10.1.015003
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author Kwon, Junhwan
Lee, Sungho
Jo, Yongjae
Choi, Myunghwan
author_facet Kwon, Junhwan
Lee, Sungho
Jo, Yongjae
Choi, Myunghwan
author_sort Kwon, Junhwan
collection PubMed
description SIGNIFICANCE: In the mammalian brain, rapid conduction of neural information is supported by the myelin, the functional efficacy of which shows steep dependence on its nanoscale cytoarchitecture. Although previous in vitro studies have suggested that neural activity accompanies nanometer-scale cellular deformations, whether neural activity can dynamically remodel the myelinated axon has remained unexplored due to the technical challenge in observing its nanostructural dynamics in living tissues. AIM: We aim to observe activity-dependent nanostructural dynamics of myelinated axons in a living brain tissue. APPROACH: We introduced a novel all-optical approach combining a nanoscale dynamic readout based on spectral interferometry and optogenetic control of neural excitation in an acute brain slice preparation. RESULTS: In response to optogenetically evoked neuronal burst firing, the myelinated axons exhibited progressive and reversible spectral redshifts, corresponding to the transient swelling at a subnanometer scale. We further revealed that the activity-dependent nanostructural dynamics was localized to the paranode. CONCLUSIONS: Our all-optical studies substantiate that myelinated axon exhibits activity-dependent nanoscale swelling, which potentially serves to dynamically tune the transmission speed of neural information.
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spelling pubmed-98682872023-01-24 All-optical observation on activity-dependent nanoscale dynamics of myelinated axons Kwon, Junhwan Lee, Sungho Jo, Yongjae Choi, Myunghwan Neurophotonics Research Papers SIGNIFICANCE: In the mammalian brain, rapid conduction of neural information is supported by the myelin, the functional efficacy of which shows steep dependence on its nanoscale cytoarchitecture. Although previous in vitro studies have suggested that neural activity accompanies nanometer-scale cellular deformations, whether neural activity can dynamically remodel the myelinated axon has remained unexplored due to the technical challenge in observing its nanostructural dynamics in living tissues. AIM: We aim to observe activity-dependent nanostructural dynamics of myelinated axons in a living brain tissue. APPROACH: We introduced a novel all-optical approach combining a nanoscale dynamic readout based on spectral interferometry and optogenetic control of neural excitation in an acute brain slice preparation. RESULTS: In response to optogenetically evoked neuronal burst firing, the myelinated axons exhibited progressive and reversible spectral redshifts, corresponding to the transient swelling at a subnanometer scale. We further revealed that the activity-dependent nanostructural dynamics was localized to the paranode. CONCLUSIONS: Our all-optical studies substantiate that myelinated axon exhibits activity-dependent nanoscale swelling, which potentially serves to dynamically tune the transmission speed of neural information. Society of Photo-Optical Instrumentation Engineers 2023-01-23 2023-01 /pmc/articles/PMC9868287/ /pubmed/36699624 http://dx.doi.org/10.1117/1.NPh.10.1.015003 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 International License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle Research Papers
Kwon, Junhwan
Lee, Sungho
Jo, Yongjae
Choi, Myunghwan
All-optical observation on activity-dependent nanoscale dynamics of myelinated axons
title All-optical observation on activity-dependent nanoscale dynamics of myelinated axons
title_full All-optical observation on activity-dependent nanoscale dynamics of myelinated axons
title_fullStr All-optical observation on activity-dependent nanoscale dynamics of myelinated axons
title_full_unstemmed All-optical observation on activity-dependent nanoscale dynamics of myelinated axons
title_short All-optical observation on activity-dependent nanoscale dynamics of myelinated axons
title_sort all-optical observation on activity-dependent nanoscale dynamics of myelinated axons
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868287/
https://www.ncbi.nlm.nih.gov/pubmed/36699624
http://dx.doi.org/10.1117/1.NPh.10.1.015003
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