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Dual-Activatable Cell Tracker for Controlled and Prolonged Single-Cell Labeling
[Image: see text] Cell trackers are fluorescent chemical tools that facilitate imaging and tracking cells within live organisms. Despite their versatility, these dyes lack specificity, tend to leak outside of the cell, and stain neighboring cells. Here, we report a dual-activatable cell tracker for...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7309267/ https://www.ncbi.nlm.nih.gov/pubmed/32298071 http://dx.doi.org/10.1021/acschembio.0c00208 |
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author | Halabi, Elias A. Arasa, Jorge Püntener, Salome Collado-Diaz, Victor Halin, Cornelia Rivera-Fuentes, Pablo |
author_facet | Halabi, Elias A. Arasa, Jorge Püntener, Salome Collado-Diaz, Victor Halin, Cornelia Rivera-Fuentes, Pablo |
author_sort | Halabi, Elias A. |
collection | PubMed |
description | [Image: see text] Cell trackers are fluorescent chemical tools that facilitate imaging and tracking cells within live organisms. Despite their versatility, these dyes lack specificity, tend to leak outside of the cell, and stain neighboring cells. Here, we report a dual-activatable cell tracker for increased spatial and temporal staining control, especially for single-cell tracking. This probe overcomes the typical problems of current cell trackers: off-target staining, high background signal, and leakage from the intracellular medium. Staining with this dye is not cytotoxic, and it can be used in sensitive primary cells. Moreover, this dye is resistant to harsh fixation and permeabilization conditions and allows for multiwavelength studies with confocal microscopy and fluorescence-activated cell sorting. Using this cell tracker, we performed in vivo homing experiments in mice with primary splenocytes and tracked a single cell in a heterogeneous, multicellular culture environment for over 20 h. These experiments, in addition to comparative proliferation studies with other cell trackers, demonstrated that the signal from this dye is retained in cells for over 72 h after photoactivation. We envision that this type of probes will facilitate the analysis of single-cell behavior and migration in cell culture and in vivo experiments. |
format | Online Article Text |
id | pubmed-7309267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73092672020-06-23 Dual-Activatable Cell Tracker for Controlled and Prolonged Single-Cell Labeling Halabi, Elias A. Arasa, Jorge Püntener, Salome Collado-Diaz, Victor Halin, Cornelia Rivera-Fuentes, Pablo ACS Chem Biol [Image: see text] Cell trackers are fluorescent chemical tools that facilitate imaging and tracking cells within live organisms. Despite their versatility, these dyes lack specificity, tend to leak outside of the cell, and stain neighboring cells. Here, we report a dual-activatable cell tracker for increased spatial and temporal staining control, especially for single-cell tracking. This probe overcomes the typical problems of current cell trackers: off-target staining, high background signal, and leakage from the intracellular medium. Staining with this dye is not cytotoxic, and it can be used in sensitive primary cells. Moreover, this dye is resistant to harsh fixation and permeabilization conditions and allows for multiwavelength studies with confocal microscopy and fluorescence-activated cell sorting. Using this cell tracker, we performed in vivo homing experiments in mice with primary splenocytes and tracked a single cell in a heterogeneous, multicellular culture environment for over 20 h. These experiments, in addition to comparative proliferation studies with other cell trackers, demonstrated that the signal from this dye is retained in cells for over 72 h after photoactivation. We envision that this type of probes will facilitate the analysis of single-cell behavior and migration in cell culture and in vivo experiments. American Chemical Society 2020-04-16 2020-06-19 /pmc/articles/PMC7309267/ /pubmed/32298071 http://dx.doi.org/10.1021/acschembio.0c00208 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Halabi, Elias A. Arasa, Jorge Püntener, Salome Collado-Diaz, Victor Halin, Cornelia Rivera-Fuentes, Pablo Dual-Activatable Cell Tracker for Controlled and Prolonged Single-Cell Labeling |
title | Dual-Activatable Cell Tracker for Controlled and Prolonged
Single-Cell Labeling |
title_full | Dual-Activatable Cell Tracker for Controlled and Prolonged
Single-Cell Labeling |
title_fullStr | Dual-Activatable Cell Tracker for Controlled and Prolonged
Single-Cell Labeling |
title_full_unstemmed | Dual-Activatable Cell Tracker for Controlled and Prolonged
Single-Cell Labeling |
title_short | Dual-Activatable Cell Tracker for Controlled and Prolonged
Single-Cell Labeling |
title_sort | dual-activatable cell tracker for controlled and prolonged
single-cell labeling |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7309267/ https://www.ncbi.nlm.nih.gov/pubmed/32298071 http://dx.doi.org/10.1021/acschembio.0c00208 |
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