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The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules

Tubular cell apoptosis is a major phenotype of cell death in various forms of acute kidney injury. Quantifying apoptosis in fixed tissues is problematic because apoptosis evolves over time and dead cells are rapidly cleared by the phagocytic system. Phiphilux is a fluorescent probe that is activated...

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Detalles Bibliográficos
Autores principales: Hato, Takashi, Sandoval, Ruben, Dagher, Pierre C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082132/
https://www.ncbi.nlm.nih.gov/pubmed/27795874
http://dx.doi.org/10.1080/21659087.2015.1067352
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author Hato, Takashi
Sandoval, Ruben
Dagher, Pierre C
author_facet Hato, Takashi
Sandoval, Ruben
Dagher, Pierre C
author_sort Hato, Takashi
collection PubMed
description Tubular cell apoptosis is a major phenotype of cell death in various forms of acute kidney injury. Quantifying apoptosis in fixed tissues is problematic because apoptosis evolves over time and dead cells are rapidly cleared by the phagocytic system. Phiphilux is a fluorescent probe that is activated specifically by caspase 3 and does not inhibit the subsequent activity of this effector caspase. It has been used successfully to quantify apoptosis in cell culture. Here we examined the feasibility of using Phiphilux to measure renal tubular apoptosis progression over time in live animals using intravital 2-photon microscopy. Our results show that Phiphilux can detect apoptosis in S2 tubules but is activated non-specifically in S1 tubules.
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spelling pubmed-50821322016-10-27 The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules Hato, Takashi Sandoval, Ruben Dagher, Pierre C Intravital Short Paper Tubular cell apoptosis is a major phenotype of cell death in various forms of acute kidney injury. Quantifying apoptosis in fixed tissues is problematic because apoptosis evolves over time and dead cells are rapidly cleared by the phagocytic system. Phiphilux is a fluorescent probe that is activated specifically by caspase 3 and does not inhibit the subsequent activity of this effector caspase. It has been used successfully to quantify apoptosis in cell culture. Here we examined the feasibility of using Phiphilux to measure renal tubular apoptosis progression over time in live animals using intravital 2-photon microscopy. Our results show that Phiphilux can detect apoptosis in S2 tubules but is activated non-specifically in S1 tubules. Taylor & Francis 2015-08-28 /pmc/articles/PMC5082132/ /pubmed/27795874 http://dx.doi.org/10.1080/21659087.2015.1067352 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Short Paper
Hato, Takashi
Sandoval, Ruben
Dagher, Pierre C
The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules
title The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules
title_full The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules
title_fullStr The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules
title_full_unstemmed The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules
title_short The caspase 3 sensor Phiphilux G2D2 is activated non-specifically in S1 renal proximal tubules
title_sort caspase 3 sensor phiphilux g2d2 is activated non-specifically in s1 renal proximal tubules
topic Short Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082132/
https://www.ncbi.nlm.nih.gov/pubmed/27795874
http://dx.doi.org/10.1080/21659087.2015.1067352
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