Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Gynecology, Maternal and Child Health Hospital of Hubei Province, Wuhan, China.
Aging Cell. 2024 Nov;23(11):e14293. doi: 10.1111/acel.14293. Epub 2024 Aug 9.
The senescence of bone marrow mesenchymal stem cells (BMSCs) contributes to the development of degenerative skeletal conditions. To date, the molecular mechanism resulting in BMSC senescence has not been fully understood. In this study, we identified a small non-coding RNA, miR-203-3p, the expression of which was elevated in BMSCs from aged mice. On the other hand, overexpression of miR-203-3p in BMSCs from young mice reduced cell growth and enhanced their senescence. Mechanistically, PDZ-linked kinase (PBK) is predicted to be the target of miR-203-3p. The binding of miR-203-3p to Pbk mRNA could decrease its expression, which in turn inhibited the ubiquitination-mediated degradation of p53. Furthermore, the intravitreal injection of miR-203-3p-inhibitor into the bone marrow cavity of aged mice attenuated BMSC senescence and osteoporosis in aged mice. Collectively, these findings suggest that targeting miR-203-3p to delay BMSC senescence could be a potential therapeutic strategy to alleviate age-related osteoporosis.
骨髓间充质干细胞(BMSCs)的衰老导致退行性骨骼疾病的发生。迄今为止,导致 BMSC 衰老的分子机制尚未完全阐明。在这项研究中,我们鉴定出一种小的非编码 RNA,miR-203-3p,其在老年小鼠的 BMSCs 中表达上调。另一方面,在年轻小鼠的 BMSCs 中过表达 miR-203-3p 会降低细胞生长并促进其衰老。从机制上讲,PDZ 连接激酶(PBK)被预测为 miR-203-3p 的靶标。miR-203-3p 与 Pbk mRNA 的结合可以降低其表达,进而抑制 p53 的泛素化介导的降解。此外,将 miR-203-3p 抑制剂注入老年小鼠的骨髓腔可减轻老年小鼠的 BMSC 衰老和骨质疏松症。总之,这些发现表明,针对 miR-203-3p 以延缓 BMSC 衰老可能是缓解与年龄相关的骨质疏松症的一种潜在治疗策略。