Interleukin-15 responses to aging and unloading-induced skeletal muscle atrophy

Emidio E Pistilli1, Parco M Siu, Stephen E Alway

  • 1Laboratory of Muscle Biology and Sarcopenia, Division of Exercise Physiology, West Virginia University School of Medicine, Robert C. Byrd Health Sciences Center, Morgantown, WV 26506-9227, USA.

Insights

Skeletal muscle aging and unloading may increase Interleukin-15 (IL-15) mRNA expression, potentially to counteract muscle loss. This study investigated IL-15

Area of Science:

  • Muscle physiology
  • Molecular biology
  • Aging research

Background:

  • Interleukin-15 (IL-15) mRNA is present in skeletal muscle.
  • IL-15 shows potential anti-apoptotic and hypertrophic effects in vitro.
  • Its in vivo role in skeletal muscle cells remains unclear.

Purpose of the Study:

  • To investigate if skeletal muscle aging and unloading alter basal IL-15 expression.
  • To determine if skeletal muscle expresses a functional IL-15 receptor (IL-15R).

Main Methods:

  • Used hindlimb suspension in rats and wing unloading in quail as unloading models.
  • Assessed muscle wet weight and IL-15 mRNA expression.
  • Examined expression of IL-15 receptor components (IL-15Ralpha, IL-2/15R-beta, -gammac).

Main Results:

  • Aged rats had less muscle mass than young rats; unloading reduced muscle mass in young but not aged rats.
  • A significant interaction between aging and unloading affected IL-15 mRNA in rat muscles.
  • Aged quail muscles showed greater resistance to unloading-induced atrophy and altered IL-15 mRNA expression compared to young quail.
  • Skeletal muscle expressed mRNA for a functional IL-15 receptor.

Conclusions:

  • IL-15 mRNA expression may increase in response to muscle atrophy stimuli.
  • This increase might be an adaptive mechanism to mitigate muscle mass loss, particularly in older animals.
  • Further research is needed to understand the IL-15/IL-15R system's role in preventing muscle wasting.