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Preparation and Culture of Myogenic Precursor Cells/Primary Myoblasts from Skeletal Muscle of Adult and Aged Humans
Published on: February 16, 2017
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.
Abstract:
Interleukin-15 (IL-15) mRNA is constitutively expressed in skeletal muscle. Although IL-15 has proposed hypertrophic and anti-apoptotic roles in vitro, its role in skeletal muscle cells in vivo is less clear. The purpose of this study was to determine if skeletal muscle aging and unloading, two conditions known to promote muscle atrophy, would alter basal IL-15 expression in skeletal muscle. We hypothesized that IL-15 mRNA expression would increase as a result of both aging and muscle unloading and that muscle would express the mRNA for a functional trimeric IL-15 receptor (IL-15R). Two models of unloading were used in this study: hindlimb suspension (HS) in rats and wing unloading in quail. The absolute muscle wet weight of plantaris and soleus muscles from aged rats was significantly less when compared with muscles from young adult rats. Although 14 days of HS resulted in reduced muscle mass of plantaris and soleus muscles from young adult animals, this effect was not observed in muscles from aged animals. A significant aging times unloading interaction was observed for IL-15 mRNA in both rat soleus and plantaris muscles. Patagialis (PAT) muscles from aged quail retained a significant 12 and 6% of stretch-induced hypertrophy after 7 and 14 days of unloading, respectively. PAT muscles from young quail retained 15% hypertrophy at 7 days of unloading but regressed to control levels following 14 days of unloading. A main effect of age was observed on IL-15 mRNA expression in PAT muscles at 14 days of overload, 7 days of unloading, and 14 days of unloading. Skeletal muscle also expressed the mRNAs for a functional IL-15R composed of IL-15Ralpha, IL-2/15R-beta, and -gammac. Based on these data, we speculate that increases in IL-15 mRNA in response to atrophic stimuli may be an attempt to counteract muscle mass loss in skeletal muscles of old animals. Additional research is warranted to determine the importance of the IL-15/IL-15R system to counter muscle wasting.
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.
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