Age-associated miRNA alterations in skeletal muscle from rhesus monkeys reversed by caloric restriction

Evi M Mercken1, Elisa Majounie, Jinhui Ding

  • 1Experimental Gerontology Section, Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.

Aging
|September 17, 2013
PubMed

Insights

Skeletal muscle aging alters microRNA (miRNA) levels in rhesus monkeys. Caloric restriction (CR) partially reversed these age-related changes, suggesting a younger muscle phenotype.

Area of Science:

  • Molecular Biology
  • Aging Research
  • Genomics

Background:

  • MicroRNA (miRNA) expression profiles change with age and in conditions like cancer and senescence.
  • Skeletal muscle aging is associated with altered gene expression, impacting muscle function and health.
  • Understanding miRNA dynamics during aging is crucial for developing interventions.

Purpose of the Study:

  • To identify differentially expressed miRNAs in skeletal muscle of young versus old rhesus monkeys.
  • To investigate the impact of caloric restriction (CR) on age-associated miRNA changes in skeletal muscle.
  • To explore the potential of CR in reversing age-related miRNA alterations.

Main Methods:

  • RNA sequencing was employed to profile miRNA expression in skeletal muscle from young and old rhesus monkeys.
  • Reverse transcription quantitative PCR (RT-qPCR) was used to validate and quantify specific miRNA levels.
  • Caloric restriction (CR) intervention was applied to assess its effects on miRNA abundance.

Main Results:

  • Several miRNAs, including miR-451, miR-144, miR-18a, and miR-15a, were upregulated in old muscle.
  • miR-181a and miR-181b were found to be downregulated in aged skeletal muscle.
  • CR intervention rescued miR-181b and chr1:205580546 levels and reduced the age-induced increase in miR-451 and miR-144.

Conclusions:

  • Skeletal muscle aging is characterized by significant alterations in both known and novel miRNA expression.
  • Caloric restriction demonstrates a capacity to ameliorate some age-related miRNA changes, promoting a younger muscle phenotype.
  • These findings highlight the role of miRNAs in the aging process and the potential therapeutic benefits of CR.