Cargando…
Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice
Learning is thought to involve changes in glutamate receptors at synapses, submicron structures that mediate communication between neurons in the central nervous system. Due to their small size and high density, synapses are difficult to resolve in vivo, limiting our ability to directly relate recep...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250193/ https://www.ncbi.nlm.nih.gov/pubmed/37169928 http://dx.doi.org/10.1038/s41592-023-01871-6 |
_version_ | 1785055702854664192 |
---|---|
author | Xu, Yu Kang T. Graves, Austin R. Coste, Gabrielle I. Huganir, Richard L. Bergles, Dwight E. Charles, Adam S. Sulam, Jeremias |
author_facet | Xu, Yu Kang T. Graves, Austin R. Coste, Gabrielle I. Huganir, Richard L. Bergles, Dwight E. Charles, Adam S. Sulam, Jeremias |
author_sort | Xu, Yu Kang T. |
collection | PubMed |
description | Learning is thought to involve changes in glutamate receptors at synapses, submicron structures that mediate communication between neurons in the central nervous system. Due to their small size and high density, synapses are difficult to resolve in vivo, limiting our ability to directly relate receptor dynamics to animal behavior. Here we developed a combination of computational and biological methods to overcome these challenges. First, we trained a deep-learning image-restoration algorithm that combines the advantages of ex vivo super-resolution and in vivo imaging modalities to overcome limitations specific to each optical system. When applied to in vivo images from transgenic mice expressing fluorescently labeled glutamate receptors, this restoration algorithm super-resolved synapses, enabling the tracking of behavior-associated synaptic plasticity with high spatial resolution. This method demonstrates the capabilities of image enhancement to learn from ex vivo data and imaging techniques to improve in vivo imaging resolution. |
format | Online Article Text |
id | pubmed-10250193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-102501932023-06-10 Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice Xu, Yu Kang T. Graves, Austin R. Coste, Gabrielle I. Huganir, Richard L. Bergles, Dwight E. Charles, Adam S. Sulam, Jeremias Nat Methods Article Learning is thought to involve changes in glutamate receptors at synapses, submicron structures that mediate communication between neurons in the central nervous system. Due to their small size and high density, synapses are difficult to resolve in vivo, limiting our ability to directly relate receptor dynamics to animal behavior. Here we developed a combination of computational and biological methods to overcome these challenges. First, we trained a deep-learning image-restoration algorithm that combines the advantages of ex vivo super-resolution and in vivo imaging modalities to overcome limitations specific to each optical system. When applied to in vivo images from transgenic mice expressing fluorescently labeled glutamate receptors, this restoration algorithm super-resolved synapses, enabling the tracking of behavior-associated synaptic plasticity with high spatial resolution. This method demonstrates the capabilities of image enhancement to learn from ex vivo data and imaging techniques to improve in vivo imaging resolution. Nature Publishing Group US 2023-05-11 2023 /pmc/articles/PMC10250193/ /pubmed/37169928 http://dx.doi.org/10.1038/s41592-023-01871-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Xu, Yu Kang T. Graves, Austin R. Coste, Gabrielle I. Huganir, Richard L. Bergles, Dwight E. Charles, Adam S. Sulam, Jeremias Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice |
title | Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice |
title_full | Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice |
title_fullStr | Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice |
title_full_unstemmed | Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice |
title_short | Cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice |
title_sort | cross-modality supervised image restoration enables nanoscale tracking of synaptic plasticity in living mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250193/ https://www.ncbi.nlm.nih.gov/pubmed/37169928 http://dx.doi.org/10.1038/s41592-023-01871-6 |
work_keys_str_mv | AT xuyukangt crossmodalitysupervisedimagerestorationenablesnanoscaletrackingofsynapticplasticityinlivingmice AT gravesaustinr crossmodalitysupervisedimagerestorationenablesnanoscaletrackingofsynapticplasticityinlivingmice AT costegabriellei crossmodalitysupervisedimagerestorationenablesnanoscaletrackingofsynapticplasticityinlivingmice AT huganirrichardl crossmodalitysupervisedimagerestorationenablesnanoscaletrackingofsynapticplasticityinlivingmice AT berglesdwighte crossmodalitysupervisedimagerestorationenablesnanoscaletrackingofsynapticplasticityinlivingmice AT charlesadams crossmodalitysupervisedimagerestorationenablesnanoscaletrackingofsynapticplasticityinlivingmice AT sulamjeremias crossmodalitysupervisedimagerestorationenablesnanoscaletrackingofsynapticplasticityinlivingmice |