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Updated: Jul 15, 2025

Magnetic-Activated Cell Sorting Strategies to Isolate and Purify Synovial Fluid-Derived Mesenchymal Stem Cells from a Rabbit Model
Published on: August 10, 2018
Rejuvenation of Senescent Mesenchymal Stem Cells to Prevent Age-Related Changes in Synovial Joints
Tatiana Sekelova1,2, Lubos Danisovic1,2, Michaela Cehakova1,2
1National Institute of Rheumatic Diseases, Piestany, Slovakia.
Abstract:
Mesenchymal/medicinal stem/signaling cells (MSCs), well known for regenerative potential, have been involved in hundreds of clinical trials. Even if equipped with reparative properties, aging significantly decreases their biological activity, representing a major challenge for MSC-based therapies. Age-related joint diseases, such as osteoarthritis, are associated with the accumulation of senescent cells, including synovial MSCs. An impaired ability of MSCs to self-renew and differentiate is one of the main contributors to the human aging process. Moreover, senescent MSCs (sMSCs) are characterized by the senescence-messaging secretome (SMS), which is typically manifested by the release of molecules with an adverse effect. Many factors, from genetic and metabolic pathways to environmental stressors, participate in the regulation of the senescent phenotype of MSCs. To better understand cellular senescence in MSCs, this review discusses the characteristics of sMSCs, their role in cartilage and synovial joint aging, and current rejuvenation approaches to delay/reverse age-related pathological changes, providing evidence from in vivo experiments as well.
Insights
Aging diminishes the regenerative capacity of mesenchymal stem cells (MSCs), impacting therapies. This review explores senescent MSCs (sMSCs) and rejuvenation strategies for joint aging.
Area of Science:
- Cellular biology
- Regenerative medicine
- Gerontology
Background:
- Mesenchymal stem cells (MSCs) possess regenerative potential but decline with age.
- Cellular senescence, particularly in synovial MSCs, contributes to age-related joint diseases like osteoarthritis.
- Senescent MSCs (sMSCs) exhibit altered self-renewal, differentiation, and secrete detrimental factors (senescence-messaging secretome).
Purpose of the Study:
- To review the characteristics of senescent MSCs (sMSCs).
- To elucidate the role of sMSCs in cartilage and synovial joint aging.
- To discuss current rejuvenation strategies for age-related pathological changes in MSCs.
Main Methods:
- Literature review focusing on cellular senescence in MSCs.
- Analysis of factors regulating the senescent phenotype in MSCs.
- Inclusion of evidence from in vivo experiments.
Main Results:
- Aging impairs MSC biological activity, posing challenges for regenerative therapies.
- Senescent MSCs contribute to the aging of cartilage and synovial joints.
- The senescence-messaging secretome of sMSCs has adverse effects.
Conclusions:
- Understanding sMSC characteristics is crucial for addressing age-related joint degeneration.
- Rejuvenation approaches offer potential to delay or reverse MSC aging.
- Further research into MSC senescence and rejuvenation is warranted for therapeutic advancements.
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