表观遗传学
平衡
间充质干细胞
DNA甲基化
骨质疏松症
干细胞
生物
骨髓
骨愈合
骨重建
组蛋白
细胞生物学
医学
生物信息学
生理学
内分泌学
免疫学
遗传学
基因表达
基因
作者
Yunyu Zhong,Xueer Zhou,Zijian Pan,Jiankang Zhang,Jian Pan
标识
DOI:10.1096/fj.202302665r
摘要
Abstract 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.
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