ID | 116581 |
Title Alternative | 老齢マウスにおいてMuRF1欠乏は筋ミトコンドリア内のPDK4蓄積を介して加齢による脂肪増加を抑制する
MuRF1 regulates lipid metabolism
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Author |
Sugiura, Kosuke
Tokushima University
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Maeda, Tasuku
Tokushima University
Uchida, Takayuki
Tokushima University
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Kishimoto, Koji
Tokushima University
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Oarada, Motoko
Sagami Women's University
Labeit, Siegfried
University of Heidelberg
Ulla, Anayt
Tokushima University
Nakao, Reiko
Tokushima University
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Sairyo, Koichi
Tokushima University
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Keywords | Muscle atrophy
Muscle RING finger 1 (MuRF1)
lipid metabolism
Pyruvate dehydrogenase kinase 4 (PDK4)
SUMO modification
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Content Type |
Thesis or Dissertation
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Description | Recent studies show that muscle mass and metabolic function are interlinked. Muscle RING finger 1 (MuRF1) is a critical muscle-specific ubiquitin ligase associated with muscle atrophy. Yet, the molecular target of MuRF1 in atrophy and aging remains unclear. We examined the role of MuRF1 in aging, using MuRF1-deficient (MuRF1–/–) mice in vivo, and MuRF1-overexpressing cell in vitro. MuRF1 deficiency partially prevents age-induced skeletal muscle loss in mice. Interestingly, body weight and fat mass of >7-month-old MuRF1–/– mice were lower than in MuRF1+/+ mice. Serum and muscle metabolic parameters and results of indirect calorimetry suggest significantly higher energy expenditure and enhanced lipid metabolism in 3-month-old MuRF1–/– mice than in MuRF1+/+ mice, resulting in suppressed adipose tissue gain during aging. Pyruvate dehydrogenase kinase 4 (PDK4) is crucial for a switch from glucose to lipid metabolism, and the interaction between MuRF1 and PDK4 was examined. PDK4 protein levels were elevated in mitochondria from the skeletal muscle in MuRF1–/– mice. In vitro, MuRF1 interacted with PDK4 but did not induce degradation through ubiquitination. Instead, SUMOylation of PDK4 was detected in MuRF1-overexpressing cells, in contrast to cells without the RING domain of MuRF1. MuRF1 deficiency enhances lipid metabolism possibly by upregulating PDK4 localization into mitochondrial through prevention of SUMOylation. Inhibition of MuRF1-mediated PDK4 SUMOylation is a potential therapeutic target for age-related dysfunction of lipid metabolism and muscle atrophy.
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Journal Title |
Journal of Orthopaedic Research
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ISSN | 1554527X
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NCID | AA10625350
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Publisher | Wiley|Orthopaedic Research Society
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Volume | 40
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Issue | 5
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Start Page | 1026
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End Page | 1038
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Published Date | 2021-06-29
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Remark | 内容要旨・審査要旨・論文本文の公開
本論文は,著者Kosuke Sugiuraの学位論文として提出され,学位審査・授与の対象となっている。 This is the peer reviewed version of the following article: Sugiura, K, Hirasaka, K, Maeda, T, et al. MuRF1 deficiency prevents age-related fat weight gain, possibly through accumulation of PDK4 in skeletal muscle mitochondria in older mice. J Orthop Res. 2022; 40: 1026-1038, which has been published in final form at https://doi.org/10.1002/jor.25131. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wileyʼs version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited. |
Rights | © 2021 Orthopaedic Research Society. Published by Wiley Periodicals LLC
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EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
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TextVersion |
ETD
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MEXT report number | 甲第3562号
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Diploma Number | 甲医第1514号
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Granted Date | 2021-11-25
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Degree Name |
Doctor of Medical Science
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Grantor |
Tokushima University
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departments |
University Hospital
Medical Sciences
Bioscience and Bioindustry
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