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Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time
Bioresponsive NIR-fluorophores offer the possibility for continual visualization of dynamic cellular processes with added potential for direct translation to in vivo imaging. Here we show the design, synthesis and lysosome-responsive emission properties of a new NIR fluorophore. The NIR fluorescent...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773516/ https://www.ncbi.nlm.nih.gov/pubmed/26927507 http://dx.doi.org/10.1038/ncomms10855 |
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author | Grossi, Marco Morgunova, Marina Cheung, Shane Scholz, Dimitri Conroy, Emer Terrile, Marta Panarella, Angela Simpson, Jeremy C. Gallagher, William M. O'Shea, Donal F. |
author_facet | Grossi, Marco Morgunova, Marina Cheung, Shane Scholz, Dimitri Conroy, Emer Terrile, Marta Panarella, Angela Simpson, Jeremy C. Gallagher, William M. O'Shea, Donal F. |
author_sort | Grossi, Marco |
collection | PubMed |
description | Bioresponsive NIR-fluorophores offer the possibility for continual visualization of dynamic cellular processes with added potential for direct translation to in vivo imaging. Here we show the design, synthesis and lysosome-responsive emission properties of a new NIR fluorophore. The NIR fluorescent probe design differs from typical amine functionalized lysosomotropic stains with off/on fluorescence switching controlled by a reversible phenol/phenolate interconversion. Emission from the probe is shown to be highly selective for the lysosomes in co-imaging experiments using a HeLa cell line expressing the lysosomal-associated membrane protein 1 fused to green fluorescent protein. The responsive probe is capable of real-time continuous imaging of fundamental cellular processes such as endocytosis, lysosomal trafficking and efflux in 3D and 4D. The advantage of the NIR emission allows for direct translation to in vivo tumour imaging, which is successfully demonstrated using an MDA-MB-231 subcutaneous tumour model. This bioresponsive NIR fluorophore offers significant potential for use in live cellular and in vivo imaging, for which currently there is a deficit of suitable molecular fluorescent tools. |
format | Online Article Text |
id | pubmed-4773516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47735162016-03-04 Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time Grossi, Marco Morgunova, Marina Cheung, Shane Scholz, Dimitri Conroy, Emer Terrile, Marta Panarella, Angela Simpson, Jeremy C. Gallagher, William M. O'Shea, Donal F. Nat Commun Article Bioresponsive NIR-fluorophores offer the possibility for continual visualization of dynamic cellular processes with added potential for direct translation to in vivo imaging. Here we show the design, synthesis and lysosome-responsive emission properties of a new NIR fluorophore. The NIR fluorescent probe design differs from typical amine functionalized lysosomotropic stains with off/on fluorescence switching controlled by a reversible phenol/phenolate interconversion. Emission from the probe is shown to be highly selective for the lysosomes in co-imaging experiments using a HeLa cell line expressing the lysosomal-associated membrane protein 1 fused to green fluorescent protein. The responsive probe is capable of real-time continuous imaging of fundamental cellular processes such as endocytosis, lysosomal trafficking and efflux in 3D and 4D. The advantage of the NIR emission allows for direct translation to in vivo tumour imaging, which is successfully demonstrated using an MDA-MB-231 subcutaneous tumour model. This bioresponsive NIR fluorophore offers significant potential for use in live cellular and in vivo imaging, for which currently there is a deficit of suitable molecular fluorescent tools. Nature Publishing Group 2016-03-01 /pmc/articles/PMC4773516/ /pubmed/26927507 http://dx.doi.org/10.1038/ncomms10855 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Grossi, Marco Morgunova, Marina Cheung, Shane Scholz, Dimitri Conroy, Emer Terrile, Marta Panarella, Angela Simpson, Jeremy C. Gallagher, William M. O'Shea, Donal F. Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time |
title | Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time |
title_full | Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time |
title_fullStr | Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time |
title_full_unstemmed | Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time |
title_short | Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time |
title_sort | lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773516/ https://www.ncbi.nlm.nih.gov/pubmed/26927507 http://dx.doi.org/10.1038/ncomms10855 |
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