Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis

Abstract Background Sarcopenia, the age‐related decline in skeletal muscle mass and function, diminishes life quality in elderly people. Improving the capacity of skeletal muscle differentiation is expected to counteract sarcopenia. However, the mechanisms underlying skeletal muscle differentiation...

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Main Authors: Xuan Jiang, Siyu Ji, Fenglai Yuan, Tushuai Li, Siyuan Cui, Wei Wang, Xianlong Ye, Rong Wang, Yongquan Chen, Shenglong Zhu
Format: Article
Language:English
Published: Wiley 2023-02-01
Series:Journal of Cachexia, Sarcopenia and Muscle
Subjects:
Online Access:https://doi.org/10.1002/jcsm.13166
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author Xuan Jiang
Siyu Ji
Fenglai Yuan
Tushuai Li
Siyuan Cui
Wei Wang
Xianlong Ye
Rong Wang
Yongquan Chen
Shenglong Zhu
author_facet Xuan Jiang
Siyu Ji
Fenglai Yuan
Tushuai Li
Siyuan Cui
Wei Wang
Xianlong Ye
Rong Wang
Yongquan Chen
Shenglong Zhu
author_sort Xuan Jiang
collection DOAJ
description Abstract Background Sarcopenia, the age‐related decline in skeletal muscle mass and function, diminishes life quality in elderly people. Improving the capacity of skeletal muscle differentiation is expected to counteract sarcopenia. However, the mechanisms underlying skeletal muscle differentiation are complex, and effective therapeutic targets are largely unknown. Methods The human Gene Expression Omnibus database, aged mice and primary skeletal muscle cells were used to assess the expression level of pyruvate dehydrogenase B (PDHB) in human and mouse aged state. d‐Galactose (d‐gal)‐induced sarcopenia mouse model and two classic cell models (C2C12 and HSkMC) were used to assess the myogenic effect of PDHB and the underlying mechanisms via immunocytochemistry, western blotting, quantitative real‐time polymerase chain reaction, RNA interference or overexpression, dual‐luciferase reporter assay, RNA sequencing and untargeted metabolomics. Results We identified that a novel target PDHB promoted myogenic differentiation. PDHB expression decreased in aged mouse muscle relative to the young state (−50% of mRNA level, P < 0.01) and increased during mouse and primary human muscle cell differentiation (+3.97‐fold, P < 0.001 and +3.79‐fold, P < 0.001). Knockdown or overexpression of PDHB modulated the expression of genes related to muscle differentiation, namely, myogenic factor 5 (Myf5) (−46%, P < 0.01 and −27%, P < 0.05; +1.8‐fold, P < 0.01), myogenic differentiation (MyoD) (−55%, P < 0.001 and −34%, P < 0.01; +2.27‐fold, P < 0.001), myogenin (MyoG) (−60%, P < 0.001 and −70%, P < 0.001; +5.46‐fold, P < 0.001) and myosin heavy chain (MyHC) (−70%, P < 0.001 and −69%, P < 0.001; +3.44‐fold, P < 0.001) in both C2C12 cells and HSkMC. Metabolomic and transcriptomic analyses revealed that PDHB knockdown suppressed pyruvate metabolism (P < 0.001) and up‐regulated ariadne RBR E3 ubiquitin protein ligase 2 (Arih2) (+7.23‐fold, P < 0.001) in cellular catabolic pathways. The role of forkhead box P1 (FoxP1) (+4.18‐fold, P < 0.001)‐mediated Arih2 transcription was the key downstream regulator of PDHB in muscle differentiation. PDHB overexpression improved d‐gal‐induced muscle atrophy in mice, which was characterized by significant increases in grip strength, muscle mass and mean muscle cross‐sectional area (1.19‐fold to 1.5‐fold, P < 0.01, P < 0.05 and P < 0.001). Conclusions The comprehensive results show that PDHB plays a sarcoprotective role by suppressing the FoxP1–Arih2 axis and may serve as a therapeutic target in sarcopenia.
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spelling doaj.art-b0becbc21879477b99f9ecc02852e6a22023-06-13T07:50:50ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092023-02-0114160662110.1002/jcsm.13166Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axisXuan Jiang0Siyu Ji1Fenglai Yuan2Tushuai Li3Siyuan Cui4Wei Wang5Xianlong Ye6Rong Wang7Yongquan Chen8Shenglong Zhu9Wuxi School of Medicine Jiangnan University Wuxi ChinaWuxi School of Medicine Jiangnan University Wuxi ChinaWuxi School of Medicine Jiangnan University Wuxi ChinaWuxi School of Medicine Jiangnan University Wuxi ChinaWuxi No. 2 People's Hospital Wuxi ChinaWuxi School of Medicine Jiangnan University Wuxi ChinaGanjiang Chinese Medicine Innovation Center Nanchang ChinaWuxi School of Medicine Jiangnan University Wuxi ChinaWuxi School of Medicine Jiangnan University Wuxi ChinaWuxi School of Medicine Jiangnan University Wuxi ChinaAbstract Background Sarcopenia, the age‐related decline in skeletal muscle mass and function, diminishes life quality in elderly people. Improving the capacity of skeletal muscle differentiation is expected to counteract sarcopenia. However, the mechanisms underlying skeletal muscle differentiation are complex, and effective therapeutic targets are largely unknown. Methods The human Gene Expression Omnibus database, aged mice and primary skeletal muscle cells were used to assess the expression level of pyruvate dehydrogenase B (PDHB) in human and mouse aged state. d‐Galactose (d‐gal)‐induced sarcopenia mouse model and two classic cell models (C2C12 and HSkMC) were used to assess the myogenic effect of PDHB and the underlying mechanisms via immunocytochemistry, western blotting, quantitative real‐time polymerase chain reaction, RNA interference or overexpression, dual‐luciferase reporter assay, RNA sequencing and untargeted metabolomics. Results We identified that a novel target PDHB promoted myogenic differentiation. PDHB expression decreased in aged mouse muscle relative to the young state (−50% of mRNA level, P < 0.01) and increased during mouse and primary human muscle cell differentiation (+3.97‐fold, P < 0.001 and +3.79‐fold, P < 0.001). Knockdown or overexpression of PDHB modulated the expression of genes related to muscle differentiation, namely, myogenic factor 5 (Myf5) (−46%, P < 0.01 and −27%, P < 0.05; +1.8‐fold, P < 0.01), myogenic differentiation (MyoD) (−55%, P < 0.001 and −34%, P < 0.01; +2.27‐fold, P < 0.001), myogenin (MyoG) (−60%, P < 0.001 and −70%, P < 0.001; +5.46‐fold, P < 0.001) and myosin heavy chain (MyHC) (−70%, P < 0.001 and −69%, P < 0.001; +3.44‐fold, P < 0.001) in both C2C12 cells and HSkMC. Metabolomic and transcriptomic analyses revealed that PDHB knockdown suppressed pyruvate metabolism (P < 0.001) and up‐regulated ariadne RBR E3 ubiquitin protein ligase 2 (Arih2) (+7.23‐fold, P < 0.001) in cellular catabolic pathways. The role of forkhead box P1 (FoxP1) (+4.18‐fold, P < 0.001)‐mediated Arih2 transcription was the key downstream regulator of PDHB in muscle differentiation. PDHB overexpression improved d‐gal‐induced muscle atrophy in mice, which was characterized by significant increases in grip strength, muscle mass and mean muscle cross‐sectional area (1.19‐fold to 1.5‐fold, P < 0.01, P < 0.05 and P < 0.001). Conclusions The comprehensive results show that PDHB plays a sarcoprotective role by suppressing the FoxP1–Arih2 axis and may serve as a therapeutic target in sarcopenia.https://doi.org/10.1002/jcsm.13166ageingmyogenesisPDHBsarcopenia
spellingShingle Xuan Jiang
Siyu Ji
Fenglai Yuan
Tushuai Li
Siyuan Cui
Wei Wang
Xianlong Ye
Rong Wang
Yongquan Chen
Shenglong Zhu
Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis
Journal of Cachexia, Sarcopenia and Muscle
ageing
myogenesis
PDHB
sarcopenia
title Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis
title_full Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis
title_fullStr Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis
title_full_unstemmed Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis
title_short Pyruvate dehydrogenase B regulates myogenic differentiation via the FoxP1–Arih2 axis
title_sort pyruvate dehydrogenase b regulates myogenic differentiation via the foxp1 arih2 axis
topic ageing
myogenesis
PDHB
sarcopenia
url https://doi.org/10.1002/jcsm.13166
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