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Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells
Coumarins have attracted intense interest in recent years due to their apoptogenic effects. The aim of the present study was to determine whether 7-hydroxycoumarin (7-HC) induces changes in caspase-3 (C-3) activity in A549 human lung carcinoma cells. A range of analytical techniques, including color...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665690/ https://www.ncbi.nlm.nih.gov/pubmed/26640551 http://dx.doi.org/10.3892/etm.2015.2765 |
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author | SOTO-NUÑEZ, MARIBEL DÍAZ-MORALES, KAREN AZUCENA CUAUTLE-RODRÍGUEZ, PATRICIA TORRES-FLORES, VÍCTOR LÓPEZ-GONZÁLEZ, JOSÉ SULLIVAN MANDOKI-WEITZNER, JUAN JOSÉ MOLINA-GUARNEROS, JUAN ARCADIO |
author_facet | SOTO-NUÑEZ, MARIBEL DÍAZ-MORALES, KAREN AZUCENA CUAUTLE-RODRÍGUEZ, PATRICIA TORRES-FLORES, VÍCTOR LÓPEZ-GONZÁLEZ, JOSÉ SULLIVAN MANDOKI-WEITZNER, JUAN JOSÉ MOLINA-GUARNEROS, JUAN ARCADIO |
author_sort | SOTO-NUÑEZ, MARIBEL |
collection | PubMed |
description | Coumarins have attracted intense interest in recent years due to their apoptogenic effects. The aim of the present study was to determine whether 7-hydroxycoumarin (7-HC) induces changes in caspase-3 (C-3) activity in A549 human lung carcinoma cells. A range of analytical techniques, including colorimetric and fluorometric assays, western blotting, single-cell microinjection, fluorescence microscopy and image analysis were conducted to elucidate the effects of 7-HC. A 24-h exposure to 1.85 mM 7-HC induced a 65% increase in C-3 activity, and a notable conversion of procaspase-3 to C-3, in addition to poly(ADP-ribose)polymerase cleavage. Furthermore, morphological changes associated with apoptosis were observed. Exposure of the cells to 7-HC for 3 or 6 h increased calcium conductance by 27%. By performing the single-cell microinjection of a specific fluorescent substrate of C-3 into previously 7-HC-exposed cells, a typical enzymatic kinetic profile of C-3 activation was identified a number of hours prior to the morphological and biochemical changes associated with apoptosis being observed. These results suggest that the rapid in vivo activation of C-3 is induced by 7-HC, the most relevant biotransformation product of coumarin in humans. |
format | Online Article Text |
id | pubmed-4665690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-46656902015-12-04 Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells SOTO-NUÑEZ, MARIBEL DÍAZ-MORALES, KAREN AZUCENA CUAUTLE-RODRÍGUEZ, PATRICIA TORRES-FLORES, VÍCTOR LÓPEZ-GONZÁLEZ, JOSÉ SULLIVAN MANDOKI-WEITZNER, JUAN JOSÉ MOLINA-GUARNEROS, JUAN ARCADIO Exp Ther Med Articles Coumarins have attracted intense interest in recent years due to their apoptogenic effects. The aim of the present study was to determine whether 7-hydroxycoumarin (7-HC) induces changes in caspase-3 (C-3) activity in A549 human lung carcinoma cells. A range of analytical techniques, including colorimetric and fluorometric assays, western blotting, single-cell microinjection, fluorescence microscopy and image analysis were conducted to elucidate the effects of 7-HC. A 24-h exposure to 1.85 mM 7-HC induced a 65% increase in C-3 activity, and a notable conversion of procaspase-3 to C-3, in addition to poly(ADP-ribose)polymerase cleavage. Furthermore, morphological changes associated with apoptosis were observed. Exposure of the cells to 7-HC for 3 or 6 h increased calcium conductance by 27%. By performing the single-cell microinjection of a specific fluorescent substrate of C-3 into previously 7-HC-exposed cells, a typical enzymatic kinetic profile of C-3 activation was identified a number of hours prior to the morphological and biochemical changes associated with apoptosis being observed. These results suggest that the rapid in vivo activation of C-3 is induced by 7-HC, the most relevant biotransformation product of coumarin in humans. D.A. Spandidos 2015-11 2015-09-23 /pmc/articles/PMC4665690/ /pubmed/26640551 http://dx.doi.org/10.3892/etm.2015.2765 Text en Copyright: © Soto-Nuñez et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles SOTO-NUÑEZ, MARIBEL DÍAZ-MORALES, KAREN AZUCENA CUAUTLE-RODRÍGUEZ, PATRICIA TORRES-FLORES, VÍCTOR LÓPEZ-GONZÁLEZ, JOSÉ SULLIVAN MANDOKI-WEITZNER, JUAN JOSÉ MOLINA-GUARNEROS, JUAN ARCADIO Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells |
title | Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells |
title_full | Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells |
title_fullStr | Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells |
title_full_unstemmed | Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells |
title_short | Single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in A549 cancer cells |
title_sort | single-cell microinjection assay indicates that 7-hydroxycoumarin induces rapid activation of caspase-3 in a549 cancer cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4665690/ https://www.ncbi.nlm.nih.gov/pubmed/26640551 http://dx.doi.org/10.3892/etm.2015.2765 |
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