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An authentic imaging probe to track cell fate from beginning to end

Accurate tracing of cell viability is critical for optimizing delivery methods, and evaluating the efficacy and safety of cell therapeutics. A nanoparticle-based cell tracker is developed to image cell fate from live to dead. The particle is fabricated from two types of optically quenched polyelectr...

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Detalles Bibliográficos
Autores principales: Lee, Seung Koo, Mortensen, Luke J., Lin, Charles P., Tung, Ching-Hsuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852472/
https://www.ncbi.nlm.nih.gov/pubmed/25323442
http://dx.doi.org/10.1038/ncomms6216
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author Lee, Seung Koo
Mortensen, Luke J.
Lin, Charles P.
Tung, Ching-Hsuan
author_facet Lee, Seung Koo
Mortensen, Luke J.
Lin, Charles P.
Tung, Ching-Hsuan
author_sort Lee, Seung Koo
collection PubMed
description Accurate tracing of cell viability is critical for optimizing delivery methods, and evaluating the efficacy and safety of cell therapeutics. A nanoparticle-based cell tracker is developed to image cell fate from live to dead. The particle is fabricated from two types of optically quenched polyelectrolytes, a life indicator and a death indicator, through electrostatic interactions. Upon incubation with cells, the fabricated bifunctional nanoprobes are taken up efficiently, and the first color is produced by normal intracellular proteolysis, reflecting the healthy status of the cells. Depending on the number of coated layers, the signal can persist for several replication cycles. However, as the cells begin dying, the second color appears quickly to reflect the new cell status. Using this chameleon-like cell tracker, live cells can be distinguished from apoptotic and necrotic cells instantly and definitively.
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spelling pubmed-48524722016-05-02 An authentic imaging probe to track cell fate from beginning to end Lee, Seung Koo Mortensen, Luke J. Lin, Charles P. Tung, Ching-Hsuan Nat Commun Article Accurate tracing of cell viability is critical for optimizing delivery methods, and evaluating the efficacy and safety of cell therapeutics. A nanoparticle-based cell tracker is developed to image cell fate from live to dead. The particle is fabricated from two types of optically quenched polyelectrolytes, a life indicator and a death indicator, through electrostatic interactions. Upon incubation with cells, the fabricated bifunctional nanoprobes are taken up efficiently, and the first color is produced by normal intracellular proteolysis, reflecting the healthy status of the cells. Depending on the number of coated layers, the signal can persist for several replication cycles. However, as the cells begin dying, the second color appears quickly to reflect the new cell status. Using this chameleon-like cell tracker, live cells can be distinguished from apoptotic and necrotic cells instantly and definitively. 2014-10-17 /pmc/articles/PMC4852472/ /pubmed/25323442 http://dx.doi.org/10.1038/ncomms6216 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Lee, Seung Koo
Mortensen, Luke J.
Lin, Charles P.
Tung, Ching-Hsuan
An authentic imaging probe to track cell fate from beginning to end
title An authentic imaging probe to track cell fate from beginning to end
title_full An authentic imaging probe to track cell fate from beginning to end
title_fullStr An authentic imaging probe to track cell fate from beginning to end
title_full_unstemmed An authentic imaging probe to track cell fate from beginning to end
title_short An authentic imaging probe to track cell fate from beginning to end
title_sort authentic imaging probe to track cell fate from beginning to end
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852472/
https://www.ncbi.nlm.nih.gov/pubmed/25323442
http://dx.doi.org/10.1038/ncomms6216
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