4.6 Article

MicroRNAs are critical regulators of senescence and aging in mesenchymal stem cells

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BONE
卷 142, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bone.2020.115679

关键词

MicroRNAs; Senescence; Aging; Mesenchymal stem cells

资金

  1. National Institutes of Health [AG036675]

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miRNAs and cellular senescence have been implicated in driving age-related diseases, particularly in mesenchymal stem cells. Differential expression of key miRNAs in MSCs and other musculoskeletal cells during senescence and aging, regulation of miRNAs via SASP cytokines, and targeting of components of cell cycle arrest pathways by miRNAs have been identified. Identifying potential miRNA targets may have implications for regenerative medicine applications in age-related musculoskeletal diseases.
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.

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