Key Components of Human Myofibre Denervation and Neuromuscular Junction Stability are Modulated by Age and Exercise.
acetylcholine receptor
cell culture
denervation
heavy resistance exercise
myogenesis
neonatal myosin
neural cell adhesion molecule
neuromuscular junction
sarcopenia
Journal
Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052
Informations de publication
Date de publication:
06 04 2020
06 04 2020
Historique:
received:
28
02
2020
revised:
25
03
2020
accepted:
03
04
2020
entrez:
10
4
2020
pubmed:
10
4
2020
medline:
17
3
2021
Statut:
epublish
Résumé
The decline in muscle mass and function with age is partly caused by a loss of muscle fibres through denervation. The purpose of this study was to investigate the potential of exercise to influence molecular targets involved in neuromuscular junction (NMJ) stability in healthy elderly individuals. Participants from two studies (one group of 12 young and 12 elderly females and another group of 25 elderly males) performed a unilateral bout of resistance exercise. Muscle biopsies were collected at 4.5 h and up to 7 days post exercise for tissue analysis and cell culture. Molecular targets related to denervation and NMJ stability were analysed by immunohistochemistry and real-time reverse transcription polymerase chain reaction. In addition to a greater presence of denervated fibres, the muscle samples and cultured myotubes from the elderly individuals displayed altered gene expression levels of acetylcholine receptor (AChR) subunits. A single bout of exercise induced general changes in AChR subunit gene expression within the biopsy sampling timeframe, suggesting a sustained plasticity of the NMJ in elderly individuals. These data support the role of exercise in maintaining NMJ stability, even in elderly inactive individuals. Furthermore, the cell culture findings suggest that the transcriptional capacity of satellite cells for AChR subunit genes is negatively affected by ageing.
Identifiants
pubmed: 32268508
pii: cells9040893
doi: 10.3390/cells9040893
pmc: PMC7226801
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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