State Key Laboratory of Oral Diseases, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Department of Oral and Maxillofacial Surgery, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China.
FASEB J. 2024 May 15;38(9):e23642. doi: 10.1096/fj.202302665R.
Alterations to the human organism that are brought about by aging are comprehensive and detrimental. Of these, an imbalance in bone homeostasis is a major outward manifestation of aging. In older adults, the decreased osteogenic activity of bone marrow mesenchymal stem cells and the inhibition of bone marrow mesenchymal stem cell differentiation lead to decreased bone mass, increased risk of fracture, and impaired bone injury healing. In the past decades, numerous studies have reported the epigenetic alterations that occur during aging, such as decreased core histones, altered DNA methylation patterns, and abnormalities in noncoding RNAs, which ultimately lead to genomic abnormalities and affect the expression of downstream signaling osteoporosis treatment and promoter of fracture healing in older adults. The current review summarizes the impact of epigenetic regulation mechanisms on age-related bone homeostasis imbalance.
衰老引起的人体变化是全面而有害的。其中,骨内稳态失衡是衰老的一个主要外在表现。在老年人中,骨髓间充质干细胞的成骨活性降低和骨髓间充质干细胞分化受到抑制,导致骨量减少、骨折风险增加和骨损伤愈合受损。在过去几十年中,大量研究报道了衰老过程中发生的表观遗传改变,如核心组蛋白减少、DNA 甲基化模式改变和非编码 RNA 异常,最终导致基因组异常,并影响下游信号转导骨质疏松症治疗和促进老年人骨折愈合的表达。本综述总结了表观遗传调控机制对与年龄相关的骨内稳态失衡的影响。