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NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates
Vasculature architecture of the brain can provide revealing information about mental and neurological function and disease. Fluorescence imaging in the second near-infrared (NIR-II) regime with less light scattering is a more promising method for detecting cortical vessels than traditional visible a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086344/ https://www.ncbi.nlm.nih.gov/pubmed/32226552 http://dx.doi.org/10.7150/thno.43533 |
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author | Cai, Zhaochong Zhu, Liang Wang, Mengqi Roe, Anna Wang Xi, Wang Qian, Jun |
author_facet | Cai, Zhaochong Zhu, Liang Wang, Mengqi Roe, Anna Wang Xi, Wang Qian, Jun |
author_sort | Cai, Zhaochong |
collection | PubMed |
description | Vasculature architecture of the brain can provide revealing information about mental and neurological function and disease. Fluorescence imaging in the second near-infrared (NIR-II) regime with less light scattering is a more promising method for detecting cortical vessels than traditional visible and NIR-I modes. Methods: Clinically approved dye indocyanine green (ICG) was used for NIR-II fluorescence imaging. Here, for the first time, we developed two NIR-II fluorescence microscopy systems for brain vasculature imaging in macaque monkeys. The first is a wide-field microscope with high temporal resolution for measuring blood flow velocity and cardiac impulse period, while the second is a high spatial resolution confocal microscope producing three-dimensional maps of the cortical microvascular network. Both were designed with flexibility to image various cortical locations on the head. Results: Here, ICG was proved to have high brightness in NIR-II region and an 8-fold QY increase in serum than in water. We achieved cerebrovascular functional imaging of monkey with high temporal resolution (25 frames/second) with wide-field microscope. The blood flow velocity of capillaries can be precisely calculated and the cardiac impulse period can be monitored as well. In vivo structural imaging of cerebrovasculature was accomplished with both high spatial lateral resolution (~8 µm) and high signal to background ratio (SBR). Vivid 3D reconstructed NIR-II fluorescence confocal microscopic images up to depth of 470 μm were also realized. Conclusion: This work comprises an important advance towards studies of neurovascular coupling, stroke, and other diseases relevant to neurovascular health in humans. |
format | Online Article Text |
id | pubmed-7086344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-70863442020-03-27 NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates Cai, Zhaochong Zhu, Liang Wang, Mengqi Roe, Anna Wang Xi, Wang Qian, Jun Theranostics Research Paper Vasculature architecture of the brain can provide revealing information about mental and neurological function and disease. Fluorescence imaging in the second near-infrared (NIR-II) regime with less light scattering is a more promising method for detecting cortical vessels than traditional visible and NIR-I modes. Methods: Clinically approved dye indocyanine green (ICG) was used for NIR-II fluorescence imaging. Here, for the first time, we developed two NIR-II fluorescence microscopy systems for brain vasculature imaging in macaque monkeys. The first is a wide-field microscope with high temporal resolution for measuring blood flow velocity and cardiac impulse period, while the second is a high spatial resolution confocal microscope producing three-dimensional maps of the cortical microvascular network. Both were designed with flexibility to image various cortical locations on the head. Results: Here, ICG was proved to have high brightness in NIR-II region and an 8-fold QY increase in serum than in water. We achieved cerebrovascular functional imaging of monkey with high temporal resolution (25 frames/second) with wide-field microscope. The blood flow velocity of capillaries can be precisely calculated and the cardiac impulse period can be monitored as well. In vivo structural imaging of cerebrovasculature was accomplished with both high spatial lateral resolution (~8 µm) and high signal to background ratio (SBR). Vivid 3D reconstructed NIR-II fluorescence confocal microscopic images up to depth of 470 μm were also realized. Conclusion: This work comprises an important advance towards studies of neurovascular coupling, stroke, and other diseases relevant to neurovascular health in humans. Ivyspring International Publisher 2020-03-04 /pmc/articles/PMC7086344/ /pubmed/32226552 http://dx.doi.org/10.7150/thno.43533 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Cai, Zhaochong Zhu, Liang Wang, Mengqi Roe, Anna Wang Xi, Wang Qian, Jun NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates |
title | NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates |
title_full | NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates |
title_fullStr | NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates |
title_full_unstemmed | NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates |
title_short | NIR-II fluorescence microscopic imaging of cortical vasculature in non-human primates |
title_sort | nir-ii fluorescence microscopic imaging of cortical vasculature in non-human primates |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086344/ https://www.ncbi.nlm.nih.gov/pubmed/32226552 http://dx.doi.org/10.7150/thno.43533 |
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