Extracellular serine and glycine are required for mouse and human skeletal muscle stem and progenitor cell function

• Published in: Molecular metabolism (Germany) 2021-01, Vol.43, p.101106-101106, Article 101106
• Main Authors: Gheller, Brandon J., Blum, Jamie E., Lim, Esther W., Handzlik, Michal K., Hannah Fong, Ern Hwei, Ko, Anthony C., Khanna, Shray, Gheller, Molly E., Bender, Erica L., Alexander, Matthew S., Stover, Patrick J., Field, Martha S., Cosgrove, Benjamin D., Metallo, Christian M., Thalacker-Mercer, Anna E.
• Format: Article
• Language: English
• Subjects: Adult; Aged; Animals; Cell Differentiation; Cell Proliferation; Cells, Cultured; Female; Glycine - metabolism; Humans; Male; Mice; Mice, Inbred C57BL; Muscle; Muscle Development - physiology; Muscle metabolism; Muscle progenitor cell; Muscle regeneration; Muscle stem cell; Muscle, Skeletal - metabolism; Muscle, Skeletal - physiology; Myoblasts - cytology; Original; Primary Cell Culture; Proliferation; Protein synthesis; Regeneration - physiology; Serine - metabolism; Stem Cells - metabolism; Stem Cells - pathology
• ISSN: 2212-8778; 2212-8778
• DOI: 10.1016/j.molmet.2020.101106

Skeletal muscle regeneration relies on muscle-specific adult stem cells (MuSCs), MuSC progeny, muscle progenitor cells (MPCs), and a coordinated myogenic program that is influenced by the extracellular environment. Following injury, MPCs undergo a transient and rapid period of population expansion, which is necessary to repair damaged myofibers and restore muscle homeostasis. Certain pathologies (e.g., metabolic diseases and muscle dystrophies) and advanced age are associated with dysregulated muscle regeneration. The availability of serine and glycine, two nutritionally non-essential amino acids, is altered in humans with these pathologies, and these amino acids have been shown to influence the proliferative state of non-muscle cells. Our objective was to determine the role of serine/glycine in MuSC/MPC function. Primary human MPCs (hMPCs) were used for in vitro experiments, and young (4–6 mo) and old (>20 mo) mice were used for in vivo experiments. Serine/glycine availability was manipulated using specially formulated media in vitro or dietary restriction in vivo followed by downstream metabolic and cell proliferation analyses. We identified that serine/glycine are essential for hMPC proliferation. Dietary restriction of serine/glycine in a mouse model of skeletal muscle regeneration lowered the abundance of MuSCs 3 days post-injury. Stable isotope-tracing studies showed that hMPCs rely on extracellular serine/glycine for population expansion because they exhibit a limited capacity for de novo serine/glycine biosynthesis. Restriction of serine/glycine to hMPCs resulted in cell cycle arrest in G0/G1. Extracellular serine/glycine was necessary to support glutathione and global protein synthesis in hMPCs. Using an aged mouse model, we found that reduced serine/glycine availability augmented intermyocellular adipocytes 28 days post-injury. These studies demonstrated that despite an absolute serine/glycine requirement for MuSC/MPC proliferation, de novo synthesis was inadequate to support these demands, making extracellular serine and glycine conditionally essential for efficient skeletal muscle regeneration. •Extracellular serine and glycine are necessary for muscle stem/progenitor cell population expansion.•Human muscle progenitor cells possess limited capacity for de novo serine/glycine biosynthesis.•Extracellular serine/glycine restriction increases reactive oxygen species and reduces intracellular glutathione.•Extracellular serine/glycine inhibits protei