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In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex

The post-synaptic density (PSD) is an electron dense region consisting of ~1000 proteins, found at the postsynaptic membrane of excitatory synapses, which varies in size depending upon synaptic strength. PSD95 is an abundant scaffolding protein in the PSD and assembles a family of supercomplexes com...

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Autores principales: Wegner, Waja, Mott, Alexander C., Grant, Seth G. N., Steffens, Heinz, Willig, Katrin I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760696/
https://www.ncbi.nlm.nih.gov/pubmed/29317733
http://dx.doi.org/10.1038/s41598-017-18640-z
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author Wegner, Waja
Mott, Alexander C.
Grant, Seth G. N.
Steffens, Heinz
Willig, Katrin I.
author_facet Wegner, Waja
Mott, Alexander C.
Grant, Seth G. N.
Steffens, Heinz
Willig, Katrin I.
author_sort Wegner, Waja
collection PubMed
description The post-synaptic density (PSD) is an electron dense region consisting of ~1000 proteins, found at the postsynaptic membrane of excitatory synapses, which varies in size depending upon synaptic strength. PSD95 is an abundant scaffolding protein in the PSD and assembles a family of supercomplexes comprised of neurotransmitter receptors, ion channels, as well as signalling and structural proteins. We use superresolution STED (STimulated Emission Depletion) nanoscopy to determine the size and shape of PSD95 in the anaesthetised mouse visual cortex. Adult knock-in mice expressing eGFP fused to the endogenous PSD95 protein were imaged at time points from 1 min to 6 h. Superresolved large assemblies of PSD95 show different sub-structures; most large assemblies were ring-like, some horse-shoe or figure-8 shaped, and shapes were continuous or made up of nanoclusters. The sub-structure appeared stable during the shorter (minute) time points, but after 1 h, more than 50% of the large assemblies showed a change in sub-structure. Overall, these data showed a sub-morphology of large PSD95 assemblies which undergo changes within the 6 hours of observation in the anaesthetised mouse.
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spelling pubmed-57606962018-01-17 In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex Wegner, Waja Mott, Alexander C. Grant, Seth G. N. Steffens, Heinz Willig, Katrin I. Sci Rep Article The post-synaptic density (PSD) is an electron dense region consisting of ~1000 proteins, found at the postsynaptic membrane of excitatory synapses, which varies in size depending upon synaptic strength. PSD95 is an abundant scaffolding protein in the PSD and assembles a family of supercomplexes comprised of neurotransmitter receptors, ion channels, as well as signalling and structural proteins. We use superresolution STED (STimulated Emission Depletion) nanoscopy to determine the size and shape of PSD95 in the anaesthetised mouse visual cortex. Adult knock-in mice expressing eGFP fused to the endogenous PSD95 protein were imaged at time points from 1 min to 6 h. Superresolved large assemblies of PSD95 show different sub-structures; most large assemblies were ring-like, some horse-shoe or figure-8 shaped, and shapes were continuous or made up of nanoclusters. The sub-structure appeared stable during the shorter (minute) time points, but after 1 h, more than 50% of the large assemblies showed a change in sub-structure. Overall, these data showed a sub-morphology of large PSD95 assemblies which undergo changes within the 6 hours of observation in the anaesthetised mouse. Nature Publishing Group UK 2018-01-09 /pmc/articles/PMC5760696/ /pubmed/29317733 http://dx.doi.org/10.1038/s41598-017-18640-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wegner, Waja
Mott, Alexander C.
Grant, Seth G. N.
Steffens, Heinz
Willig, Katrin I.
In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex
title In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex
title_full In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex
title_fullStr In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex
title_full_unstemmed In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex
title_short In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex
title_sort in vivo sted microscopy visualizes psd95 sub-structures and morphological changes over several hours in the mouse visual cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760696/
https://www.ncbi.nlm.nih.gov/pubmed/29317733
http://dx.doi.org/10.1038/s41598-017-18640-z
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