Exosomal circFAM63Bsuppresses bone regeneration of postmenopausal osteoporosis via regulating miR-578/HMGA2 axis.
Feng LiXiaodong ZhaoYang ZhangQingshan ZhuangSong WangXichi FangTao XuXiaopeng LiGaoyang ChenPublished in: Journal of orthopaedic research : official publication of the Orthopaedic Research Society (2024)
Postmenopausal osteoporosis (PMOP) affects hundreds of millions of elderly women worldwide. The imbalance between osteoblast-mediated bone formation and osteoclast-mediated bone resorption is the key factor in the progression of PMOP. Recently, exosomal circular RNAs have been considered as critical regulators in physiological and pathological progress. However, their roles in PMOP still require further exploration. Herein, we identified that the expression of exosomal circFAM63B significantly increased in PMOP patients and is closely related to bone density. We further demonstrated that circFAM63B inhibits osteogenic differentiation of bone marrow stromal cells and bone formation in ovariectomy mice by using a combination of in vitro and in vivo experiment strategies. Mechanistically, circFAM63B promotes HMGA2 expression by inhibiting miR-578, thereby suppressing bone repair. Our study proved that exosomal circFAM63B suppresses the bone regeneration of PMOP by regulating the miR-578/HMGA2 axis, which may provide new insights into the pathogenesis and development of PMOP. Knocking down exosomal circFAM63B could be regarded as a new strategy for the treatment of PMOP.
Keyphrases
- bone regeneration
- bone mineral density
- long non coding rna
- poor prognosis
- cell proliferation
- postmenopausal women
- bone marrow
- long noncoding rna
- bone loss
- end stage renal disease
- signaling pathway
- body composition
- chronic kidney disease
- ejection fraction
- newly diagnosed
- polycystic ovary syndrome
- peritoneal dialysis
- prognostic factors
- breast cancer risk
- transcription factor
- middle aged
- pregnancy outcomes
- replacement therapy
- patient reported
- wild type