Laboratory of Endocrinology and Metabolism, Department of Endocrinology, West China Hospital, Sichuan University, Chengdu 610041, Sichuan, People's Republic of China.
Department of Integrated Traditional Chinese and Western Medicine. West China Hospital, Sichuan University, Chengdu 610041, Sichuan, People's Republic of China.
Curr Mol Med. 2023;23(10):1046-1057. doi: 10.2174/1566524023666221025104629.
Osteoporosis is a systemic bone disease that seriously threatens the health and quality of life in middle-aged and older adults. In this review, we describe the relationship between bone marrow adipose tissue and aging osteoporosis and mainly focus on bone marrow mesenchymal stem cell osteogenic-adipose differentiation fate with aging along with the relevant mechanisms responsible for these changes.
We summarized recent advances in regulating the bone marrow mesenchymal stem cell differentiation due to aging in this review.
Aging-related bone mass loss is accompanied by expanding bone marrow adipose because of an imbalance of bone marrow mesenchymal stem cell differentiation, resulting in adipogenesis. Ectopic adipocytes in the bone marrow increase with age and are a key factor responsible for the aging-related bone mass decrease. Transcription factors and classical regulating pathways are involved in this process during aging.
As the global aging population increases, not only older women but also older men face a great fracture risk. Therefore, finding molecular mechanisms controlling the stimulating adipogenesis in BMSC during aging is important for providing the new cue for prevention and therapeutics for aging-related bone loss. Furthermore, upon physical examination of older people, except for the bone mineral density and bone turnover biochemical marker, the bone marrow adipose measurement should be taken into account when assessing the fracture risk and treatment plan that will be beneficial in clinical practice.
骨质疏松症是一种全身性骨骼疾病,严重威胁中老年人的健康和生活质量。本综述描述了骨髓脂肪组织与衰老性骨质疏松症的关系,并主要关注随衰老发生的骨髓间充质干细胞成骨-脂肪分化命运及其相关机制。
我们总结了近年来与衰老相关的骨髓间充质干细胞分化调控的新进展。
与衰老相关的骨量丢失伴随着骨髓间充质干细胞分化失衡导致的骨髓脂肪扩张,从而导致脂肪生成。骨髓中的异位脂肪细胞随年龄增长而增加,是导致与衰老相关的骨量减少的关键因素。转录因子和经典调节途径参与了这一过程。
随着全球老龄化人口的增加,不仅老年女性,而且老年男性都面临着巨大的骨折风险。因此,寻找控制衰老过程中 BMSC 中脂肪生成的分子机制对于提供预防和治疗与衰老相关的骨丢失的新线索非常重要。此外,在对老年人进行体检时,除了骨密度和骨转换生化标志物外,在评估骨折风险和治疗计划时还应考虑骨髓脂肪测量,这将有益于临床实践。