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Near-infrared bioluminescence imaging of two cell populations in living mice

Multicolor bioluminescence imaging using near-infrared emitting luciferases is an attractive application to detect two cell populations within one animal model. Herein, we describe how to distinguish dual-color bioluminescent signals co-localized in the same compartment. We tested CBG2 click beetle...

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Detalles Bibliográficos
Autores principales: Zambito, Giorgia, Mezzanotte, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273408/
https://www.ncbi.nlm.nih.gov/pubmed/34286293
http://dx.doi.org/10.1016/j.xpro.2021.100662
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author Zambito, Giorgia
Mezzanotte, Laura
author_facet Zambito, Giorgia
Mezzanotte, Laura
author_sort Zambito, Giorgia
collection PubMed
description Multicolor bioluminescence imaging using near-infrared emitting luciferases is an attractive application to detect two cell populations within one animal model. Herein, we describe how to distinguish dual-color bioluminescent signals co-localized in the same compartment. We tested CBG2 click beetle (λ = 660 nm) and CBR2 click beetle (λ = 730 nm) luciferases paired with NH(2)-NpLH2 luciferin. Following a spectral unmixing algorithm, single spectral contributions can be resolved and quantified, enabling the visualization of multiple cell types in deep tissue by injection of a single substrate. For complete details on the use and execution of this protocol, please refer to Zambito et al. (2020).
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spelling pubmed-82734082021-07-19 Near-infrared bioluminescence imaging of two cell populations in living mice Zambito, Giorgia Mezzanotte, Laura STAR Protoc Protocol Multicolor bioluminescence imaging using near-infrared emitting luciferases is an attractive application to detect two cell populations within one animal model. Herein, we describe how to distinguish dual-color bioluminescent signals co-localized in the same compartment. We tested CBG2 click beetle (λ = 660 nm) and CBR2 click beetle (λ = 730 nm) luciferases paired with NH(2)-NpLH2 luciferin. Following a spectral unmixing algorithm, single spectral contributions can be resolved and quantified, enabling the visualization of multiple cell types in deep tissue by injection of a single substrate. For complete details on the use and execution of this protocol, please refer to Zambito et al. (2020). Elsevier 2021-07-07 /pmc/articles/PMC8273408/ /pubmed/34286293 http://dx.doi.org/10.1016/j.xpro.2021.100662 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Zambito, Giorgia
Mezzanotte, Laura
Near-infrared bioluminescence imaging of two cell populations in living mice
title Near-infrared bioluminescence imaging of two cell populations in living mice
title_full Near-infrared bioluminescence imaging of two cell populations in living mice
title_fullStr Near-infrared bioluminescence imaging of two cell populations in living mice
title_full_unstemmed Near-infrared bioluminescence imaging of two cell populations in living mice
title_short Near-infrared bioluminescence imaging of two cell populations in living mice
title_sort near-infrared bioluminescence imaging of two cell populations in living mice
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273408/
https://www.ncbi.nlm.nih.gov/pubmed/34286293
http://dx.doi.org/10.1016/j.xpro.2021.100662
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