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Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism

The yeast Saccharomyces cerevisiae undergoes a mitochondrial-dependent programmed cell death in response to different stimuli, such as acetic acid, with features similar to those of mammalian apoptosis. However, the upstream signaling events in this process, including those leading to mitochondrial...

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Autores principales: Rego, António, Costa, Margarida, Chaves, Susana Rodrigues, Matmati, Nabil, Pereira, Helena, Sousa, Maria João, Moradas-Ferreira, Pedro, Hannun, Yusuf A., Costa, Vítor, Côrte-Real, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511487/
https://www.ncbi.nlm.nih.gov/pubmed/23226203
http://dx.doi.org/10.1371/journal.pone.0048571
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author Rego, António
Costa, Margarida
Chaves, Susana Rodrigues
Matmati, Nabil
Pereira, Helena
Sousa, Maria João
Moradas-Ferreira, Pedro
Hannun, Yusuf A.
Costa, Vítor
Côrte-Real, Manuela
author_facet Rego, António
Costa, Margarida
Chaves, Susana Rodrigues
Matmati, Nabil
Pereira, Helena
Sousa, Maria João
Moradas-Ferreira, Pedro
Hannun, Yusuf A.
Costa, Vítor
Côrte-Real, Manuela
author_sort Rego, António
collection PubMed
description The yeast Saccharomyces cerevisiae undergoes a mitochondrial-dependent programmed cell death in response to different stimuli, such as acetic acid, with features similar to those of mammalian apoptosis. However, the upstream signaling events in this process, including those leading to mitochondrial membrane permeabilization, are still poorly characterized. Changes in sphingolipid metabolism have been linked to modulation of apoptosis in both yeast and mammalian cells, and ceramides have been detected in mitochondria upon apoptotic stimuli. In this study, we aimed to characterize the contribution of enzymes involved in ceramide metabolism to apoptotic cell death induced by acetic acid. We show that isc1Δ and lag1Δ mutants, lacking inositol phosphosphingolipid phospholipase C and ceramide synthase, respectively, exhibited a higher resistance to acetic acid that was associated with lower levels of some phytoceramide species. Consistently, these mutant cells displayed lower levels of ROS production and reduced mitochondrial alterations, such as mitochondrial fragmentation and degradation, and decreased translocation of cytochrome c into the cytosol in response to acetic acid. These results suggest that ceramide production contributes to cell death induced by acetic acid, especially through hydrolysis of complex sphingolipids catalyzed by Isc1p and de novo synthesis catalyzed by Lag1p, and provide the first in vivo indication of its involvement in mitochondrial outer membrane permeabilization in yeast.
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spelling pubmed-35114872012-12-05 Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism Rego, António Costa, Margarida Chaves, Susana Rodrigues Matmati, Nabil Pereira, Helena Sousa, Maria João Moradas-Ferreira, Pedro Hannun, Yusuf A. Costa, Vítor Côrte-Real, Manuela PLoS One Research Article The yeast Saccharomyces cerevisiae undergoes a mitochondrial-dependent programmed cell death in response to different stimuli, such as acetic acid, with features similar to those of mammalian apoptosis. However, the upstream signaling events in this process, including those leading to mitochondrial membrane permeabilization, are still poorly characterized. Changes in sphingolipid metabolism have been linked to modulation of apoptosis in both yeast and mammalian cells, and ceramides have been detected in mitochondria upon apoptotic stimuli. In this study, we aimed to characterize the contribution of enzymes involved in ceramide metabolism to apoptotic cell death induced by acetic acid. We show that isc1Δ and lag1Δ mutants, lacking inositol phosphosphingolipid phospholipase C and ceramide synthase, respectively, exhibited a higher resistance to acetic acid that was associated with lower levels of some phytoceramide species. Consistently, these mutant cells displayed lower levels of ROS production and reduced mitochondrial alterations, such as mitochondrial fragmentation and degradation, and decreased translocation of cytochrome c into the cytosol in response to acetic acid. These results suggest that ceramide production contributes to cell death induced by acetic acid, especially through hydrolysis of complex sphingolipids catalyzed by Isc1p and de novo synthesis catalyzed by Lag1p, and provide the first in vivo indication of its involvement in mitochondrial outer membrane permeabilization in yeast. Public Library of Science 2012-11-30 /pmc/articles/PMC3511487/ /pubmed/23226203 http://dx.doi.org/10.1371/journal.pone.0048571 Text en © 2012 Rego et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rego, António
Costa, Margarida
Chaves, Susana Rodrigues
Matmati, Nabil
Pereira, Helena
Sousa, Maria João
Moradas-Ferreira, Pedro
Hannun, Yusuf A.
Costa, Vítor
Côrte-Real, Manuela
Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism
title Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism
title_full Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism
title_fullStr Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism
title_full_unstemmed Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism
title_short Modulation of Mitochondrial Outer Membrane Permeabilization and Apoptosis by Ceramide Metabolism
title_sort modulation of mitochondrial outer membrane permeabilization and apoptosis by ceramide metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511487/
https://www.ncbi.nlm.nih.gov/pubmed/23226203
http://dx.doi.org/10.1371/journal.pone.0048571
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