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Published on: June 18, 2018
miR-350-3p Contributes to Age-Associated Impairment of IL-6 Production by Macrophages
Huiying Chang1, Xu Wang1, Shusen Yang1
1a Department of Cardiology , The First Affiliated Hospital, Cardiovascular Institute, Harbin Medical University , Harbin , P.R. China.
Abstract:
Aging-associated dysfunction of the immune system contributes to the increase in pathophysiological processes that occur with age. Numerous studies have shown that microRNAs regulate immune responses, although their role in age-related macrophage dysfunction remains elusive. Here, we found that miR-350-3p is expressed at lower levels in peritoneal macrophages from aged mice compared with young mice, and that lipopolysaccharide (LPS) stimulation downregulates miR-350-3p expression to a greater extent in young macrophages compared with aged macrophages. Consequently, LPS-stimulated aged macrophages express more miR-350-3p than do similarly treated young macrophages. Luciferase reporter assays showed that interleukin (IL)-6 mRNA is a miR-350-3p target in macrophages. Furthermore, although LPS induces less IL-6 production by aged macrophages than by young macrophages, the aged cell response is rescued by production miR-350-3p inhibition. These findings suggest that miR-350-3p may contribute to age-related impairment of macrophage function and could be a novel target for the treatment of age-related inflammatory diseases.
Insights
MicroRNA miR-350-3p levels increase in aged macrophages, impairing immune responses. Inhibiting miR-350-3p may treat age-related inflammatory diseases by restoring macrophage function.
Area of Science:
- Immunology
- Molecular Biology
- Aging Research
Background:
- Immune system aging leads to increased disease risk.
- MicroRNAs regulate immune responses, but their role in aged macrophages is unclear.
Purpose of the Study:
- Investigate the role of miR-350-3p in age-related macrophage dysfunction.
- Identify miR-350-3p as a potential therapeutic target for inflammatory diseases.
Main Methods:
- Compared miR-350-3p expression in young and aged mouse macrophages.
- Utilized lipopolysaccharide (LPS) stimulation.
- Performed luciferase reporter assays to identify mRNA targets.
- Assessed interleukin-6 (IL-6) production.
Main Results:
- miR-350-3p expression is lower in aged macrophages.
- LPS stimulation causes greater miR-350-3p downregulation in young macrophages.
- Aged macrophages express higher miR-350-3p post-LPS.
- IL-6 mRNA is a miR-350-3p target.
- miR-350-3p inhibition rescues IL-6 production in aged macrophages.
Conclusions:
- miR-350-3p contributes to age-related macrophage dysfunction.
- miR-350-3p is a potential therapeutic target for age-related inflammatory conditions.
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