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Updated: May 13, 2026

Quantitative Real-Time Polymerase Chain Reaction Evaluation of MicroRNA Expression in Kidney and Serum of Mice with Age-Dependent Renal Impairment
Published on: April 29, 2022
Deep sequencing identifies circulating mouse miRNAs that are functionally implicated in manifestations of aging and
Joseph M Dhahbi1, Stephen R Spindler, Hani Atamna
1Department of Biochemistry, University of California at Riverside, Riverside, CA 92521, USA. jdhahbi@ucr.edu
Abstract:
MicroRNAs (miRNAs) function to modulate gene expression, and through this property they regulate a broad spectrum of cellular processes. They can circulate in blood and thereby mediate cell-to-cell communication. Aging involves changes in many cellular processes that are potentially regulated by miRNAs, and some evidence has implicated circulating miRNAs in the aging process. In order to initiate a comprehensive assessment of the role of circulating miRNAs in aging, we have used deep sequencing to characterize circulating miRNAs in the serum of young mice, old mice, and old mice maintained on calorie restriction (CR). Deep sequencing identifies a set of novel miRNAs, and also accurately measures all known miRNAs present in serum. This analysis demonstrates that the levels of many miRNAs circulating in the mouse are increased with age, and that the increases can be antagonized by CR. The genes targeted by this set of age-modulated miRNAs are predicted to regulate biological processes directly relevant to the manifestations of aging including metabolic changes, and the miRNAs themselves have been linked to diseases associated with old age. This finding implicates circulating miRNAs in the aging process, raising questions about their tissues of origin, their cellular targets, and their functional role in metabolic changes that occur with aging.
Insights
Circulating microRNAs (miRNAs) increase with age in mice, but calorie restriction (CR) can reverse this trend. These age-related miRNA changes are linked to aging processes and diseases.
Area of Science:
- Biochemistry
- Molecular Biology
- Gerontology
Background:
- MicroRNAs (miRNAs) regulate gene expression and cellular processes.
- Circulating miRNAs mediate cell-to-cell communication.
- Aging involves cellular changes potentially influenced by miRNAs.
Purpose of the Study:
- To comprehensively assess the role of circulating miRNAs in the aging process.
- To characterize circulating miRNAs in young, old, and calorie-restricted (CR) old mice using deep sequencing.
Main Methods:
- Deep sequencing of serum miRNAs from young mice, old mice, and old mice on CR.
- Identification of novel and quantification of known circulating miRNAs.
Main Results:
- Many circulating miRNAs increase with age in mice.
- Calorie restriction (CR) antagonizes age-related increases in circulating miRNAs.
- Genes targeted by age-modulated miRNAs are involved in aging-related biological processes, including metabolic changes.
Conclusions:
- Circulating miRNAs are implicated in the aging process.
- Age-modulated miRNAs may play a functional role in aging-related metabolic changes.
- Further research is needed on miRNA tissue of origin, cellular targets, and functional roles in aging.
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