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Cranial window for longitudinal and multimodal imaging of the whole mouse cortex
SIGNIFICANCE: All functional brain imaging methods have technical drawbacks and specific spatial and temporal resolution limitations. Unraveling brain function requires bridging the data acquired with cellular and mesoscopic functional imaging. This imposes the access to animal preparations, allowin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500537/ https://www.ncbi.nlm.nih.gov/pubmed/36159711 http://dx.doi.org/10.1117/1.NPh.9.3.031921 |
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author | Tournissac, Marine Boido, Davide Omnès, Manon Houssen, Yannick Goulam Ciobanu, Luisa Charpak, Serge |
author_facet | Tournissac, Marine Boido, Davide Omnès, Manon Houssen, Yannick Goulam Ciobanu, Luisa Charpak, Serge |
author_sort | Tournissac, Marine |
collection | PubMed |
description | SIGNIFICANCE: All functional brain imaging methods have technical drawbacks and specific spatial and temporal resolution limitations. Unraveling brain function requires bridging the data acquired with cellular and mesoscopic functional imaging. This imposes the access to animal preparations, allowing longitudinal and multiscale investigations of brain function in anesthetized and awake animals. Such preparations are optimal to study normal and pathological brain functions while reducing the number of animals used. AIM: To fulfill these needs, we developed a chronic and stable preparation for a broad set of imaging modalities and experimental design. APPROACH: We describe the detailed protocol for a chronic cranial window, transparent to light and ultrasound, devoid of BOLD functional magnetic resonance imaging (fMRI) artifact and allowing stable and longitudinal multimodal imaging of the entire mouse cortex. RESULTS: The inexpensive, transparent, and curved polymethylpentene cranial window preparation gives access to the entire mouse cortex. It is compatible with standard microscopic and mesoscopic neuroimaging methods. We present examples of data on the neurovascular unit and its activation using two-photon, functional ultrasound imaging, and BOLD fMRI. CONCLUSION: This preparation is ideal for multimodal imaging in the same animal. |
format | Online Article Text |
id | pubmed-9500537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-95005372022-09-24 Cranial window for longitudinal and multimodal imaging of the whole mouse cortex Tournissac, Marine Boido, Davide Omnès, Manon Houssen, Yannick Goulam Ciobanu, Luisa Charpak, Serge Neurophotonics Special Section on Imaging Neuroimmune, Neuroglial and Neurovascular Interfaces (Part II) SIGNIFICANCE: All functional brain imaging methods have technical drawbacks and specific spatial and temporal resolution limitations. Unraveling brain function requires bridging the data acquired with cellular and mesoscopic functional imaging. This imposes the access to animal preparations, allowing longitudinal and multiscale investigations of brain function in anesthetized and awake animals. Such preparations are optimal to study normal and pathological brain functions while reducing the number of animals used. AIM: To fulfill these needs, we developed a chronic and stable preparation for a broad set of imaging modalities and experimental design. APPROACH: We describe the detailed protocol for a chronic cranial window, transparent to light and ultrasound, devoid of BOLD functional magnetic resonance imaging (fMRI) artifact and allowing stable and longitudinal multimodal imaging of the entire mouse cortex. RESULTS: The inexpensive, transparent, and curved polymethylpentene cranial window preparation gives access to the entire mouse cortex. It is compatible with standard microscopic and mesoscopic neuroimaging methods. We present examples of data on the neurovascular unit and its activation using two-photon, functional ultrasound imaging, and BOLD fMRI. CONCLUSION: This preparation is ideal for multimodal imaging in the same animal. Society of Photo-Optical Instrumentation Engineers 2022-09-23 2022-07 /pmc/articles/PMC9500537/ /pubmed/36159711 http://dx.doi.org/10.1117/1.NPh.9.3.031921 Text en © 2022 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 | Special Section on Imaging Neuroimmune, Neuroglial and Neurovascular Interfaces (Part II) Tournissac, Marine Boido, Davide Omnès, Manon Houssen, Yannick Goulam Ciobanu, Luisa Charpak, Serge Cranial window for longitudinal and multimodal imaging of the whole mouse cortex |
title | Cranial window for longitudinal and multimodal imaging of the whole mouse cortex |
title_full | Cranial window for longitudinal and multimodal imaging of the whole mouse cortex |
title_fullStr | Cranial window for longitudinal and multimodal imaging of the whole mouse cortex |
title_full_unstemmed | Cranial window for longitudinal and multimodal imaging of the whole mouse cortex |
title_short | Cranial window for longitudinal and multimodal imaging of the whole mouse cortex |
title_sort | cranial window for longitudinal and multimodal imaging of the whole mouse cortex |
topic | Special Section on Imaging Neuroimmune, Neuroglial and Neurovascular Interfaces (Part II) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500537/ https://www.ncbi.nlm.nih.gov/pubmed/36159711 http://dx.doi.org/10.1117/1.NPh.9.3.031921 |
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