RRC ID 86005
Author Oyabu M, Sato T, Kawaguchi R, Yoshioka K, Ito N, Eguchi T, Gotoh H, Yoshizawa T, Ogawa Y, Ono Y, Miura S, Kamei Y.
Title Multi-dimensional metabolomic remodeling under diverse muscle atrophic stimuli in vivo.
Journal Cell Rep
Abstract Muscle wasting leads to reduced activities of daily living, an increased number of care-dependent individuals, and increased mortality. However, the metabolomic adaptations underlying muscle wasting remain poorly understood. Here, by comparing physiological, genetically induced, pathological, and age-related muscle atrophy, we identify the metabolites modulated by muscle atrophic stimuli, which we term "atrometabolites." Integrated metabolomics reveal that dysfunctional polyamine synthesis is a common feature of muscle atrophy. Mechanistically, we identify that adenosylmethionine decarboxylase 1 (Amd1) and Amd2 are important for maintaining polyamine metabolism and that downregulation of Amd1 and Amd2 is a trigger of myotube atrophy. Using skeletal muscle-specific FoxO triple-knockout mice, we find that FoxOs are required for immobilization-induced metabolomic remodeling and identify FoxO-dependent atrometabolites. This study comprehensively elucidates the molecular basis of muscle metabolomic adaptation and provides the datasets that will lead to the discovery of mechanisms underlying tissue adaptation to maintain homeostasis.
Volume 44(8)
Pages 116097
Published 2025-8-26
DOI 10.1016/j.celrep.2025.116097
PII S2211-1247(25)00868-X
PMID 40768332
MeSH Animals Male Metabolome* Metabolomics* / methods Mice Mice, Inbred C57BL Mice, Knockout Muscle Fibers, Skeletal / metabolism Muscle Fibers, Skeletal / pathology Muscle, Skeletal* / metabolism Muscle, Skeletal* / pathology Muscular Atrophy* / metabolism Muscular Atrophy* / pathology Polyamines / metabolism
IF 8.109
Resource
Human and Animal Cells C2C12(RCB0987)