Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging
Abstract Advances in fluorescence imaging coupled with the generation of near infrared probes have significantly improved the capabilities of non-invasive, real-time imaging in whole animals. In this study we were able to overcome a limitation of in vivo fluorescence imaging and have established a d...
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2021-01-01
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Online Access: | https://doi.org/10.1038/s41598-021-81097-8 |
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doaj-ca12ce3447e14a7b979b7355d75fee0a2021-01-17T12:38:56ZengNature Publishing GroupScientific Reports2045-23222021-01-0111111110.1038/s41598-021-81097-8Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imagingJack Leslie0Stuart M. Robinson1Fiona Oakley2Saimir Luli3Newcastle Fibrosis Research Group, Faculty of Medical Sciences, Biosciences Institute, Newcastle UniversityNewcastle Fibrosis Research Group, Faculty of Medical Sciences, Biosciences Institute, Newcastle UniversityNewcastle Fibrosis Research Group, Faculty of Medical Sciences, Biosciences Institute, Newcastle UniversityNewcastle Fibrosis Research Group, Faculty of Medical Sciences, Biosciences Institute, Newcastle UniversityAbstract Advances in fluorescence imaging coupled with the generation of near infrared probes have significantly improved the capabilities of non-invasive, real-time imaging in whole animals. In this study we were able to overcome a limitation of in vivo fluorescence imaging and have established a dual cell tracking method where two different cell types can be monitored according to the spectral signature of the cell labelling fluorophore. Using a mouse model of acute liver injury, we have characterised the in vivo migration patterns of wild type and transgenic neutrophils with impaired chemotaxis. Here, we were able to demonstrate that IVIS provides a sensitive multiplexing technology to differentiate two different cell populations based on the spectral signature of the cell labelling fluorophores. This spectral unmixing methodology has the potential to uncover multidimensional cellular interactions involved in many diseases such as fibrosis and cancer. In vivo spectral un-mixing provides a useful tool for monitoring multiple biological process in real-time in the same animal.https://doi.org/10.1038/s41598-021-81097-8 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jack Leslie Stuart M. Robinson Fiona Oakley Saimir Luli |
spellingShingle |
Jack Leslie Stuart M. Robinson Fiona Oakley Saimir Luli Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging Scientific Reports |
author_facet |
Jack Leslie Stuart M. Robinson Fiona Oakley Saimir Luli |
author_sort |
Jack Leslie |
title |
Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging |
title_short |
Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging |
title_full |
Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging |
title_fullStr |
Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging |
title_full_unstemmed |
Non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging |
title_sort |
non-invasive synchronous monitoring of neutrophil migration using whole body near-infrared fluorescence-based imaging |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-01-01 |
description |
Abstract Advances in fluorescence imaging coupled with the generation of near infrared probes have significantly improved the capabilities of non-invasive, real-time imaging in whole animals. In this study we were able to overcome a limitation of in vivo fluorescence imaging and have established a dual cell tracking method where two different cell types can be monitored according to the spectral signature of the cell labelling fluorophore. Using a mouse model of acute liver injury, we have characterised the in vivo migration patterns of wild type and transgenic neutrophils with impaired chemotaxis. Here, we were able to demonstrate that IVIS provides a sensitive multiplexing technology to differentiate two different cell populations based on the spectral signature of the cell labelling fluorophores. This spectral unmixing methodology has the potential to uncover multidimensional cellular interactions involved in many diseases such as fibrosis and cancer. In vivo spectral un-mixing provides a useful tool for monitoring multiple biological process in real-time in the same animal. |
url |
https://doi.org/10.1038/s41598-021-81097-8 |
work_keys_str_mv |
AT jackleslie noninvasivesynchronousmonitoringofneutrophilmigrationusingwholebodynearinfraredfluorescencebasedimaging AT stuartmrobinson noninvasivesynchronousmonitoringofneutrophilmigrationusingwholebodynearinfraredfluorescencebasedimaging AT fionaoakley noninvasivesynchronousmonitoringofneutrophilmigrationusingwholebodynearinfraredfluorescencebasedimaging AT saimirluli noninvasivesynchronousmonitoringofneutrophilmigrationusingwholebodynearinfraredfluorescencebasedimaging |
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1714941876619968512 |