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Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan

The mitochondrial unfolded protein response (UPR(mt)) is a stress response mediated by the expression of genes such as chaperones, proteases, and mitokines to maintain mitochondrial proteostasis. Certain genetically modified mice, which defect mitochondrial proteins specifically in adipocytes, devel...

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Detalles Bibliográficos
Autores principales: Kobayashi, Masaki, Nezu, Yuichiro, Tagawa, Ryoma, Higami, Yoshikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998111/
https://www.ncbi.nlm.nih.gov/pubmed/33799894
http://dx.doi.org/10.3390/ijms22062854
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author Kobayashi, Masaki
Nezu, Yuichiro
Tagawa, Ryoma
Higami, Yoshikazu
author_facet Kobayashi, Masaki
Nezu, Yuichiro
Tagawa, Ryoma
Higami, Yoshikazu
author_sort Kobayashi, Masaki
collection PubMed
description The mitochondrial unfolded protein response (UPR(mt)) is a stress response mediated by the expression of genes such as chaperones, proteases, and mitokines to maintain mitochondrial proteostasis. Certain genetically modified mice, which defect mitochondrial proteins specifically in adipocytes, developed atrophy of the white adipose tissue, resisted diet-induced obesity, and had altered whole-body metabolism. UPR(mt), which has beneficial functions for living organisms, is termed “mitohormesis”, but its specific characteristics and detailed regulatory mechanism have not been elucidated to date. In this review, we discuss the function of UPR(mt) in adipose atrophy (lipoatrophy), whole-body metabolism, and lifespan based on the concept of mitohormesis.
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spelling pubmed-79981112021-03-28 Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan Kobayashi, Masaki Nezu, Yuichiro Tagawa, Ryoma Higami, Yoshikazu Int J Mol Sci Review The mitochondrial unfolded protein response (UPR(mt)) is a stress response mediated by the expression of genes such as chaperones, proteases, and mitokines to maintain mitochondrial proteostasis. Certain genetically modified mice, which defect mitochondrial proteins specifically in adipocytes, developed atrophy of the white adipose tissue, resisted diet-induced obesity, and had altered whole-body metabolism. UPR(mt), which has beneficial functions for living organisms, is termed “mitohormesis”, but its specific characteristics and detailed regulatory mechanism have not been elucidated to date. In this review, we discuss the function of UPR(mt) in adipose atrophy (lipoatrophy), whole-body metabolism, and lifespan based on the concept of mitohormesis. MDPI 2021-03-11 /pmc/articles/PMC7998111/ /pubmed/33799894 http://dx.doi.org/10.3390/ijms22062854 Text en © 2021 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
Kobayashi, Masaki
Nezu, Yuichiro
Tagawa, Ryoma
Higami, Yoshikazu
Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan
title Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan
title_full Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan
title_fullStr Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan
title_full_unstemmed Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan
title_short Mitochondrial Unfolded Protein Responses in White Adipose Tissue: Lipoatrophy, Whole-Body Metabolism and Lifespan
title_sort mitochondrial unfolded protein responses in white adipose tissue: lipoatrophy, whole-body metabolism and lifespan
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998111/
https://www.ncbi.nlm.nih.gov/pubmed/33799894
http://dx.doi.org/10.3390/ijms22062854
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