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Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence
Prohibitin 1 (PHB1) is a highly conserved protein that is mainly localized to the inner mitochondrial membrane and has been implicated in regulating mitochondrial function in yeast. Because mitochondria are emerging as an important regulator of vascular homeostasis, we examined PHB1 function in endo...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213620/ https://www.ncbi.nlm.nih.gov/pubmed/18195103 http://dx.doi.org/10.1083/jcb.200706072 |
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author | Schleicher, Michael Shepherd, Benjamin R. Suarez, Yajaira Fernandez-Hernando, Carlos Yu, Jun Pan, Yong Acevedo, Lisette M. Shadel, Gerald S. Sessa, William C. |
author_facet | Schleicher, Michael Shepherd, Benjamin R. Suarez, Yajaira Fernandez-Hernando, Carlos Yu, Jun Pan, Yong Acevedo, Lisette M. Shadel, Gerald S. Sessa, William C. |
author_sort | Schleicher, Michael |
collection | PubMed |
description | Prohibitin 1 (PHB1) is a highly conserved protein that is mainly localized to the inner mitochondrial membrane and has been implicated in regulating mitochondrial function in yeast. Because mitochondria are emerging as an important regulator of vascular homeostasis, we examined PHB1 function in endothelial cells. PHB1 is highly expressed in the vascular system and knockdown of PHB1 in endothelial cells increases mitochondrial production of reactive oxygen species via inhibition of complex I, which results in cellular senescence. As a direct consequence, both Akt and Rac1 are hyperactivated, leading to cytoskeletal rearrangements and decreased endothelial cell motility, e.g., migration and tube formation. This is also reflected in an in vivo angiogenesis assay, where silencing of PHB1 blocks the formation of functional blood vessels. Collectively, our results provide evidence that PHB1 is important for mitochondrial function and prevents reactive oxygen species–induced senescence and thereby maintains the angiogenic capacity of endothelial cells. |
format | Text |
id | pubmed-2213620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22136202008-07-14 Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence Schleicher, Michael Shepherd, Benjamin R. Suarez, Yajaira Fernandez-Hernando, Carlos Yu, Jun Pan, Yong Acevedo, Lisette M. Shadel, Gerald S. Sessa, William C. J Cell Biol Research Articles Prohibitin 1 (PHB1) is a highly conserved protein that is mainly localized to the inner mitochondrial membrane and has been implicated in regulating mitochondrial function in yeast. Because mitochondria are emerging as an important regulator of vascular homeostasis, we examined PHB1 function in endothelial cells. PHB1 is highly expressed in the vascular system and knockdown of PHB1 in endothelial cells increases mitochondrial production of reactive oxygen species via inhibition of complex I, which results in cellular senescence. As a direct consequence, both Akt and Rac1 are hyperactivated, leading to cytoskeletal rearrangements and decreased endothelial cell motility, e.g., migration and tube formation. This is also reflected in an in vivo angiogenesis assay, where silencing of PHB1 blocks the formation of functional blood vessels. Collectively, our results provide evidence that PHB1 is important for mitochondrial function and prevents reactive oxygen species–induced senescence and thereby maintains the angiogenic capacity of endothelial cells. The Rockefeller University Press 2008-01-14 /pmc/articles/PMC2213620/ /pubmed/18195103 http://dx.doi.org/10.1083/jcb.200706072 Text en Copyright © 2008, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Schleicher, Michael Shepherd, Benjamin R. Suarez, Yajaira Fernandez-Hernando, Carlos Yu, Jun Pan, Yong Acevedo, Lisette M. Shadel, Gerald S. Sessa, William C. Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence |
title | Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence |
title_full | Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence |
title_fullStr | Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence |
title_full_unstemmed | Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence |
title_short | Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence |
title_sort | prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213620/ https://www.ncbi.nlm.nih.gov/pubmed/18195103 http://dx.doi.org/10.1083/jcb.200706072 |
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