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A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis

Programmed cell death or apoptosis is a central biological process that is dysregulated in many diseases, including inflammatory conditions and cancer. The detection and quantification of apoptotic cells in vivo is hampered by the need for fixatives or washing steps for non-fluorogenic reagents, and...

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Autores principales: Barth, Nicole D., Subiros-Funosas, Ramon, Mendive-Tapia, Lorena, Duffin, Rodger, Shields, Mario A., Cartwright, Jennifer A., Henriques, Sónia Troeira, Sot, Jesus, Goñi, Felix M., Lavilla, Rodolfo, Marwick, John A., Vermeren, Sonja, Rossi, Adriano G., Egeblad, Mikala, Dransfield, Ian, Vendrell, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423924/
https://www.ncbi.nlm.nih.gov/pubmed/32788676
http://dx.doi.org/10.1038/s41467-020-17772-7
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author Barth, Nicole D.
Subiros-Funosas, Ramon
Mendive-Tapia, Lorena
Duffin, Rodger
Shields, Mario A.
Cartwright, Jennifer A.
Henriques, Sónia Troeira
Sot, Jesus
Goñi, Felix M.
Lavilla, Rodolfo
Marwick, John A.
Vermeren, Sonja
Rossi, Adriano G.
Egeblad, Mikala
Dransfield, Ian
Vendrell, Marc
author_facet Barth, Nicole D.
Subiros-Funosas, Ramon
Mendive-Tapia, Lorena
Duffin, Rodger
Shields, Mario A.
Cartwright, Jennifer A.
Henriques, Sónia Troeira
Sot, Jesus
Goñi, Felix M.
Lavilla, Rodolfo
Marwick, John A.
Vermeren, Sonja
Rossi, Adriano G.
Egeblad, Mikala
Dransfield, Ian
Vendrell, Marc
author_sort Barth, Nicole D.
collection PubMed
description Programmed cell death or apoptosis is a central biological process that is dysregulated in many diseases, including inflammatory conditions and cancer. The detection and quantification of apoptotic cells in vivo is hampered by the need for fixatives or washing steps for non-fluorogenic reagents, and by the low levels of free calcium in diseased tissues that restrict the use of annexins. In this manuscript, we report the rational design of a highly stable fluorogenic peptide (termed Apo-15) that selectively stains apoptotic cells in vitro and in vivo in a calcium-independent manner and under wash-free conditions. Furthermore, using a combination of chemical and biophysical methods, we identify phosphatidylserine as a molecular target of Apo-15. We demonstrate that Apo-15 can be used for the quantification and imaging of drug-induced apoptosis in preclinical mouse models, thus creating opportunities for assessing the in vivo efficacy of anti-inflammatory and anti-cancer therapeutics.
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spelling pubmed-74239242020-08-18 A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis Barth, Nicole D. Subiros-Funosas, Ramon Mendive-Tapia, Lorena Duffin, Rodger Shields, Mario A. Cartwright, Jennifer A. Henriques, Sónia Troeira Sot, Jesus Goñi, Felix M. Lavilla, Rodolfo Marwick, John A. Vermeren, Sonja Rossi, Adriano G. Egeblad, Mikala Dransfield, Ian Vendrell, Marc Nat Commun Article Programmed cell death or apoptosis is a central biological process that is dysregulated in many diseases, including inflammatory conditions and cancer. The detection and quantification of apoptotic cells in vivo is hampered by the need for fixatives or washing steps for non-fluorogenic reagents, and by the low levels of free calcium in diseased tissues that restrict the use of annexins. In this manuscript, we report the rational design of a highly stable fluorogenic peptide (termed Apo-15) that selectively stains apoptotic cells in vitro and in vivo in a calcium-independent manner and under wash-free conditions. Furthermore, using a combination of chemical and biophysical methods, we identify phosphatidylserine as a molecular target of Apo-15. We demonstrate that Apo-15 can be used for the quantification and imaging of drug-induced apoptosis in preclinical mouse models, thus creating opportunities for assessing the in vivo efficacy of anti-inflammatory and anti-cancer therapeutics. Nature Publishing Group UK 2020-08-12 /pmc/articles/PMC7423924/ /pubmed/32788676 http://dx.doi.org/10.1038/s41467-020-17772-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Barth, Nicole D.
Subiros-Funosas, Ramon
Mendive-Tapia, Lorena
Duffin, Rodger
Shields, Mario A.
Cartwright, Jennifer A.
Henriques, Sónia Troeira
Sot, Jesus
Goñi, Felix M.
Lavilla, Rodolfo
Marwick, John A.
Vermeren, Sonja
Rossi, Adriano G.
Egeblad, Mikala
Dransfield, Ian
Vendrell, Marc
A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
title A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
title_full A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
title_fullStr A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
title_full_unstemmed A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
title_short A fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
title_sort fluorogenic cyclic peptide for imaging and quantification of drug-induced apoptosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423924/
https://www.ncbi.nlm.nih.gov/pubmed/32788676
http://dx.doi.org/10.1038/s41467-020-17772-7
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