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Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex

Mitochondrial functions are essential for life, critical for development, maintenance of stem cells, adaptation to physiological changes, responses to stress, and aging. The complexity of mitochondrial biogenesis requires coordinated nuclear and mitochondrial gene expression, owing to the need of st...

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Detalles Bibliográficos
Autores principales: Hernando-Rodríguez, Blanca, Artal-Sanz, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315423/
https://www.ncbi.nlm.nih.gov/pubmed/30501123
http://dx.doi.org/10.3390/cells7120238
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author Hernando-Rodríguez, Blanca
Artal-Sanz, Marta
author_facet Hernando-Rodríguez, Blanca
Artal-Sanz, Marta
author_sort Hernando-Rodríguez, Blanca
collection PubMed
description Mitochondrial functions are essential for life, critical for development, maintenance of stem cells, adaptation to physiological changes, responses to stress, and aging. The complexity of mitochondrial biogenesis requires coordinated nuclear and mitochondrial gene expression, owing to the need of stoichiometrically assemble the oxidative phosphorylation (OXPHOS) system for ATP production. It requires, in addition, the import of a large number of proteins from the cytosol to keep optimal mitochondrial function and metabolism. Moreover, mitochondria require lipid supply for membrane biogenesis, while it is itself essential for the synthesis of membrane lipids. To achieve mitochondrial homeostasis, multiple mechanisms of quality control have evolved to ensure that mitochondrial function meets cell, tissue, and organismal demands. Herein, we give an overview of mitochondrial mechanisms that are activated in response to stress, including mitochondrial dynamics, mitophagy and the mitochondrial unfolded protein response (UPR(mt)). We then discuss the role of these stress responses in aging, with particular focus on Caenorhabditis elegans. Finally, we review observations that point to the mitochondrial prohibitin (PHB) complex as a key player in mitochondrial homeostasis, being essential for mitochondrial biogenesis and degradation, and responding to mitochondrial stress. Understanding how mitochondria responds to stress and how such responses are regulated is pivotal to combat aging and disease.
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spelling pubmed-63154232019-01-09 Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex Hernando-Rodríguez, Blanca Artal-Sanz, Marta Cells Review Mitochondrial functions are essential for life, critical for development, maintenance of stem cells, adaptation to physiological changes, responses to stress, and aging. The complexity of mitochondrial biogenesis requires coordinated nuclear and mitochondrial gene expression, owing to the need of stoichiometrically assemble the oxidative phosphorylation (OXPHOS) system for ATP production. It requires, in addition, the import of a large number of proteins from the cytosol to keep optimal mitochondrial function and metabolism. Moreover, mitochondria require lipid supply for membrane biogenesis, while it is itself essential for the synthesis of membrane lipids. To achieve mitochondrial homeostasis, multiple mechanisms of quality control have evolved to ensure that mitochondrial function meets cell, tissue, and organismal demands. Herein, we give an overview of mitochondrial mechanisms that are activated in response to stress, including mitochondrial dynamics, mitophagy and the mitochondrial unfolded protein response (UPR(mt)). We then discuss the role of these stress responses in aging, with particular focus on Caenorhabditis elegans. Finally, we review observations that point to the mitochondrial prohibitin (PHB) complex as a key player in mitochondrial homeostasis, being essential for mitochondrial biogenesis and degradation, and responding to mitochondrial stress. Understanding how mitochondria responds to stress and how such responses are regulated is pivotal to combat aging and disease. MDPI 2018-11-29 /pmc/articles/PMC6315423/ /pubmed/30501123 http://dx.doi.org/10.3390/cells7120238 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hernando-Rodríguez, Blanca
Artal-Sanz, Marta
Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex
title Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex
title_full Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex
title_fullStr Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex
title_full_unstemmed Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex
title_short Mitochondrial Quality Control Mechanisms and the PHB (Prohibitin) Complex
title_sort mitochondrial quality control mechanisms and the phb (prohibitin) complex
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315423/
https://www.ncbi.nlm.nih.gov/pubmed/30501123
http://dx.doi.org/10.3390/cells7120238
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