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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Main Authors: Jack Leslie, Stuart M. Robinson, Fiona Oakley, Saimir Luli
Format: Article
Language:English
Published: Nature Publishing Group 2021-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-81097-8
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spelling 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
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