# mTORC1 signalling and protein synthesis are elevated in response to amino acids in human myotubes obtained from young, old, and old trained men

**Authors:** Stephanie D. Gagnon, Jiani Qian, Vladimir Belhac, Neil R. W. Martin

PMC · DOI: 10.1007/s11626-025-01041-2 · 2025-05-20

## TL;DR

This study found that muscle cells from older men respond to amino acids similarly to younger men in terms of growth signaling and protein synthesis.

## Contribution

The study is the first to show that aging and training status do not affect amino acid-induced mTORC1 signaling and protein synthesis in cultured human myotubes.

## Key findings

- Myotube diameter was lower in cultures from older individuals, but cell fusion was similar across groups.
- mTORC1 signaling and protein synthesis increased similarly in response to amino acids in young, old, and old trained men's myotubes.
- These findings suggest skeletal muscle desensitization to amino acids with aging may not occur in vitro.

## Abstract

Ageing and reduced levels of physical activity are associated with desensitisation of skeletal muscle to the anabolic effects of amino acids. In vitro studies have indicated that many properties of skeletal muscle tissue are retained in human myotubes, including metabolic alterations associated with exercise and disease. However, the interaction between ageing and physical activity on amino acid sensing and growth has not been explored in human myotubes in vitro. Muscle-derived cells were isolated from biopsies taken from eight young (Y: 23.4 ± 1.9 yr), six older (O: 72.5 ± 5.0 yr), and nine older exercise trained (OT: 71.0 ± 4.1 yr, n = 9) men, and myotube cultures were generated and investigated for growth parameters and amino acid induced changes in mTORC1 signalling and protein synthesis. Our results indicated that muscle cell fusion was similar between groups, but myotube diameter was lower in cultures derived from O individuals. Despite this, mTORC1 signalling, as indicated by immunoblots for phosphorylation of mTORSer2448, rpS6Ser235/236, and 4E-BP1Thr37/46 increased to a similar extent in response to amino acid availability in Y, O, and OT myotubes. Furthermore, measures of protein synthesis using the SUnSET assay were increased similarly between groups after the addition of amino acids. These data suggest that skeletal muscle desensitisation to amino acids with ageing is not observed in myotubes cultured in vitro, which could be reflective of the healthy individuals tested in our study or point towards the importance of the muscle niche in the impairments in muscle metabolism in ageing.

The online version contains supplementary material available at 10.1007/s11626-025-01041-2.

## Linked entities

- **Proteins:** Crtc (CREB-regulated transcription coactivator), MTOR (mechanistic target of rapamycin kinase), RPS6 (ribosomal protein S6), EIF4EBP1 (eukaryotic translation initiation factor 4E binding protein 1)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, EIF4EBP1 (eukaryotic translation initiation factor 4E binding protein 1) [NCBI Gene 1978] {aka 4E-BP1, 4EBP1, BP-1, PHAS-I}, RPS6 (ribosomal protein S6) [NCBI Gene 6194] {aka S6, eS6}
- **Diseases:** impairments in muscle metabolism (MESH:D009135)
- **Chemicals:** amino acid (MESH:D000596), SUnSET (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12975814/full.md

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Source: https://tomesphere.com/paper/PMC12975814