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Mitochondrial Fusion Is Essential for Steroid Biosynthesis

Although the contribution of mitochondrial dynamics (a balance in fusion/fission events and changes in mitochondria subcellular distribution) to key biological process has been reported, the contribution of changes in mitochondrial fusion to achieve efficient steroid production has never been explor...

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Autores principales: Duarte, Alejandra, Poderoso, Cecilia, Cooke, Mariana, Soria, Gastón, Cornejo Maciel, Fabiana, Gottifredi, Vanesa, Podestá, Ernesto J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448708/
https://www.ncbi.nlm.nih.gov/pubmed/23029265
http://dx.doi.org/10.1371/journal.pone.0045829
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author Duarte, Alejandra
Poderoso, Cecilia
Cooke, Mariana
Soria, Gastón
Cornejo Maciel, Fabiana
Gottifredi, Vanesa
Podestá, Ernesto J.
author_facet Duarte, Alejandra
Poderoso, Cecilia
Cooke, Mariana
Soria, Gastón
Cornejo Maciel, Fabiana
Gottifredi, Vanesa
Podestá, Ernesto J.
author_sort Duarte, Alejandra
collection PubMed
description Although the contribution of mitochondrial dynamics (a balance in fusion/fission events and changes in mitochondria subcellular distribution) to key biological process has been reported, the contribution of changes in mitochondrial fusion to achieve efficient steroid production has never been explored. The mitochondria are central during steroid synthesis and different enzymes are localized between the mitochondria and the endoplasmic reticulum to produce the final steroid hormone, thus suggesting that mitochondrial fusion might be relevant for this process. In the present study, we showed that the hormonal stimulation triggers mitochondrial fusion into tubular-shaped structures and we demonstrated that mitochondrial fusion does not only correlate-with but also is an essential step of steroid production, being both events depend on PKA activity. We also demonstrated that the hormone-stimulated relocalization of ERK1/2 in the mitochondrion, a critical step during steroidogenesis, depends on mitochondrial fusion. Additionally, we showed that the SHP2 phosphatase, which is required for full steroidogenesis, simultaneously modulates mitochondrial fusion and ERK1/2 localization in the mitochondrion. Strikingly, we found that mitofusin 2 (Mfn2) expression, a central protein for mitochondrial fusion, is upregulated immediately after hormone stimulation. Moreover, Mfn2 knockdown is sufficient to impair steroid biosynthesis. Together, our findings unveil an essential role for mitochondrial fusion during steroidogenesis. These discoveries highlight the importance of organelles’ reorganization in specialized cells, prompting the exploration of the impact that organelle dynamics has on biological processes that include, but are not limited to, steroid synthesis.
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spelling pubmed-34487082012-10-01 Mitochondrial Fusion Is Essential for Steroid Biosynthesis Duarte, Alejandra Poderoso, Cecilia Cooke, Mariana Soria, Gastón Cornejo Maciel, Fabiana Gottifredi, Vanesa Podestá, Ernesto J. PLoS One Research Article Although the contribution of mitochondrial dynamics (a balance in fusion/fission events and changes in mitochondria subcellular distribution) to key biological process has been reported, the contribution of changes in mitochondrial fusion to achieve efficient steroid production has never been explored. The mitochondria are central during steroid synthesis and different enzymes are localized between the mitochondria and the endoplasmic reticulum to produce the final steroid hormone, thus suggesting that mitochondrial fusion might be relevant for this process. In the present study, we showed that the hormonal stimulation triggers mitochondrial fusion into tubular-shaped structures and we demonstrated that mitochondrial fusion does not only correlate-with but also is an essential step of steroid production, being both events depend on PKA activity. We also demonstrated that the hormone-stimulated relocalization of ERK1/2 in the mitochondrion, a critical step during steroidogenesis, depends on mitochondrial fusion. Additionally, we showed that the SHP2 phosphatase, which is required for full steroidogenesis, simultaneously modulates mitochondrial fusion and ERK1/2 localization in the mitochondrion. Strikingly, we found that mitofusin 2 (Mfn2) expression, a central protein for mitochondrial fusion, is upregulated immediately after hormone stimulation. Moreover, Mfn2 knockdown is sufficient to impair steroid biosynthesis. Together, our findings unveil an essential role for mitochondrial fusion during steroidogenesis. These discoveries highlight the importance of organelles’ reorganization in specialized cells, prompting the exploration of the impact that organelle dynamics has on biological processes that include, but are not limited to, steroid synthesis. Public Library of Science 2012-09-21 /pmc/articles/PMC3448708/ /pubmed/23029265 http://dx.doi.org/10.1371/journal.pone.0045829 Text en © 2012 Duarte 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
Duarte, Alejandra
Poderoso, Cecilia
Cooke, Mariana
Soria, Gastón
Cornejo Maciel, Fabiana
Gottifredi, Vanesa
Podestá, Ernesto J.
Mitochondrial Fusion Is Essential for Steroid Biosynthesis
title Mitochondrial Fusion Is Essential for Steroid Biosynthesis
title_full Mitochondrial Fusion Is Essential for Steroid Biosynthesis
title_fullStr Mitochondrial Fusion Is Essential for Steroid Biosynthesis
title_full_unstemmed Mitochondrial Fusion Is Essential for Steroid Biosynthesis
title_short Mitochondrial Fusion Is Essential for Steroid Biosynthesis
title_sort mitochondrial fusion is essential for steroid biosynthesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448708/
https://www.ncbi.nlm.nih.gov/pubmed/23029265
http://dx.doi.org/10.1371/journal.pone.0045829
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