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Updated: Dec 6, 2025

Techniques to Induce and Quantify Cellular Senescence
Published on: May 1, 2017
MicroRNAs are critical regulators of senescence and aging in mesenchymal stem cells
Matthew L Potter1, William D Hill2, Carlos M Isales3
1Department of Orthopedics, Augusta University, Augusta, GA, United States of America.
Abstract:
MicroRNAs (miRNAs) have recently come under scrutiny for their role in various age-related diseases. Similarly, cellular senescence has been linked to disease and aging. MicroRNAs and senescence likely play an intertwined role in driving these pathologic states. In this review, we present the connection between these two drivers of age-related disease concerning mesenchymal stem cells (MSCs). First, we summarize key miRNAs that are differentially expressed in MSCs and other musculoskeletal lineage cells during senescence and aging. Additionally, we also reviewed miRNAs that are regulated via traditional senescence-associated secretory phenotype (SASP) cytokines in MSC. Lastly, we summarize miRNAs that have been found to target components of the cell cycle arrest pathways inherently activated in senescence. This review attempts to highlight potential miRNA targets for regenerative medicine applications in age-related musculoskeletal disease.
Insights
MicroRNAs (miRNAs) and cellular senescence are key drivers of age-related diseases. This review explores their intertwined roles in mesenchymal stem cells (MSCs) for potential regenerative medicine applications.
Area of Science:
- Gerontology
- Molecular Biology
- Regenerative Medicine
Background:
- Cellular senescence and microRNAs (miRNAs) are implicated in aging and age-related diseases.
- Mesenchymal stem cells (MSCs) play crucial roles in tissue repair and are affected by aging and senescence.
Purpose of the Study:
- To review the connection between miRNAs and cellular senescence in MSCs.
- To highlight potential miRNA targets for treating age-related musculoskeletal diseases.
Main Methods:
- Literature review of studies on miRNAs, senescence, and MSCs.
- Analysis of differentially expressed miRNAs in senescent and aging MSCs.
- Examination of miRNA regulation by senescence-associated secretory phenotype (SASP) factors.
- Identification of miRNAs targeting cell cycle arrest pathways in senescence.
Main Results:
- Specific miRNAs are differentially expressed during MSC senescence and aging.
- MiRNAs are regulated by SASP cytokines in MSCs.
- Several miRNAs target key components of senescence-induced cell cycle arrest pathways.
Conclusions:
- The interplay between miRNAs and senescence in MSCs is critical for age-related musculoskeletal conditions.
- Targeting specific miRNAs in MSCs offers potential for regenerative therapies in aging populations.
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