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mTOR Signaling in Metabolic Stress Adaptation

The mechanistic target of rapamycin (mTOR) is a central regulator of cellular homeostasis that integrates environmental and nutrient signals to control cell growth and survival. Over the past two decades, extensive studies of mTOR have implicated the importance of this protein complex in regulating...

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Detalles Bibliográficos
Autores principales: Wu, Cheng-Wei, Storey, Kenneth B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147357/
https://www.ncbi.nlm.nih.gov/pubmed/34062764
http://dx.doi.org/10.3390/biom11050681
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author Wu, Cheng-Wei
Storey, Kenneth B.
author_facet Wu, Cheng-Wei
Storey, Kenneth B.
author_sort Wu, Cheng-Wei
collection PubMed
description The mechanistic target of rapamycin (mTOR) is a central regulator of cellular homeostasis that integrates environmental and nutrient signals to control cell growth and survival. Over the past two decades, extensive studies of mTOR have implicated the importance of this protein complex in regulating a broad range of metabolic functions, as well as its role in the progression of various human diseases. Recently, mTOR has emerged as a key signaling molecule in regulating animal entry into a hypometabolic state as a survival strategy in response to environmental stress. Here, we review current knowledge of the role that mTOR plays in contributing to natural hypometabolic states such as hibernation, estivation, hypoxia/anoxia tolerance, and dauer diapause. Studies across a diverse range of animal species reveal that mTOR exhibits unique regulatory patterns in an environmental stressor-dependent manner. We discuss how key signaling proteins within the mTOR signaling pathways are regulated in different animal models of stress, and describe how each of these regulations uniquely contribute to promoting animal survival in a hypometabolic state.
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spelling pubmed-81473572021-05-26 mTOR Signaling in Metabolic Stress Adaptation Wu, Cheng-Wei Storey, Kenneth B. Biomolecules Review The mechanistic target of rapamycin (mTOR) is a central regulator of cellular homeostasis that integrates environmental and nutrient signals to control cell growth and survival. Over the past two decades, extensive studies of mTOR have implicated the importance of this protein complex in regulating a broad range of metabolic functions, as well as its role in the progression of various human diseases. Recently, mTOR has emerged as a key signaling molecule in regulating animal entry into a hypometabolic state as a survival strategy in response to environmental stress. Here, we review current knowledge of the role that mTOR plays in contributing to natural hypometabolic states such as hibernation, estivation, hypoxia/anoxia tolerance, and dauer diapause. Studies across a diverse range of animal species reveal that mTOR exhibits unique regulatory patterns in an environmental stressor-dependent manner. We discuss how key signaling proteins within the mTOR signaling pathways are regulated in different animal models of stress, and describe how each of these regulations uniquely contribute to promoting animal survival in a hypometabolic state. MDPI 2021-05-01 /pmc/articles/PMC8147357/ /pubmed/34062764 http://dx.doi.org/10.3390/biom11050681 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wu, Cheng-Wei
Storey, Kenneth B.
mTOR Signaling in Metabolic Stress Adaptation
title mTOR Signaling in Metabolic Stress Adaptation
title_full mTOR Signaling in Metabolic Stress Adaptation
title_fullStr mTOR Signaling in Metabolic Stress Adaptation
title_full_unstemmed mTOR Signaling in Metabolic Stress Adaptation
title_short mTOR Signaling in Metabolic Stress Adaptation
title_sort mtor signaling in metabolic stress adaptation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147357/
https://www.ncbi.nlm.nih.gov/pubmed/34062764
http://dx.doi.org/10.3390/biom11050681
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