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Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism

In all eukaryotes, the mechanistic target of rapamycin (mTOR) signaling emerges as a master regulator of homeostasis, which integrates environmental inputs, including nutrients, energy, and growth factors, to regulate many fundamental cellular processes such as cell growth and metabolism. mTOR signa...

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Detalles Bibliográficos
Autores principales: Luo, Yongting, Xu, Wenyi, Li, Guannan, Cui, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232796/
https://www.ncbi.nlm.nih.gov/pubmed/30510625
http://dx.doi.org/10.1155/2018/7838647
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author Luo, Yongting
Xu, Wenyi
Li, Guannan
Cui, Wei
author_facet Luo, Yongting
Xu, Wenyi
Li, Guannan
Cui, Wei
author_sort Luo, Yongting
collection PubMed
description In all eukaryotes, the mechanistic target of rapamycin (mTOR) signaling emerges as a master regulator of homeostasis, which integrates environmental inputs, including nutrients, energy, and growth factors, to regulate many fundamental cellular processes such as cell growth and metabolism. mTOR signaling functions through two structurally and functionally distinct complexes, mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2), which correspond to two major branches of signal output. While mTORC1 is well characterized for its structure, regulation, and function in the last decade, information of mTORC2 signaling is only rapidly expanding in recent years, from structural biology, signaling network, to functional impact. Here we review the recent advances in many aspects of the mTORC2 signaling, with particular focus on its involvement in the control of cell metabolism and its physiological implications in metabolic diseases and aging.
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spelling pubmed-62327962018-12-03 Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism Luo, Yongting Xu, Wenyi Li, Guannan Cui, Wei Oxid Med Cell Longev Review Article In all eukaryotes, the mechanistic target of rapamycin (mTOR) signaling emerges as a master regulator of homeostasis, which integrates environmental inputs, including nutrients, energy, and growth factors, to regulate many fundamental cellular processes such as cell growth and metabolism. mTOR signaling functions through two structurally and functionally distinct complexes, mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2), which correspond to two major branches of signal output. While mTORC1 is well characterized for its structure, regulation, and function in the last decade, information of mTORC2 signaling is only rapidly expanding in recent years, from structural biology, signaling network, to functional impact. Here we review the recent advances in many aspects of the mTORC2 signaling, with particular focus on its involvement in the control of cell metabolism and its physiological implications in metabolic diseases and aging. Hindawi 2018-10-30 /pmc/articles/PMC6232796/ /pubmed/30510625 http://dx.doi.org/10.1155/2018/7838647 Text en Copyright © 2018 Yongting Luo et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Luo, Yongting
Xu, Wenyi
Li, Guannan
Cui, Wei
Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism
title Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism
title_full Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism
title_fullStr Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism
title_full_unstemmed Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism
title_short Weighing In on mTOR Complex 2 Signaling: The Expanding Role in Cell Metabolism
title_sort weighing in on mtor complex 2 signaling: the expanding role in cell metabolism
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232796/
https://www.ncbi.nlm.nih.gov/pubmed/30510625
http://dx.doi.org/10.1155/2018/7838647
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