Celastrol regulates bone marrow mesenchymal stem cell fate and bone-fat balance in osteoporosis and skeletal aging by inducing PGC-1α signaling

被引:16
|
作者
Li, Li [1 ]
Wang, Bing [1 ]
Li, Yawei [1 ]
Li, Lei [1 ]
Dai, Yuliang [1 ]
Lv, Guohua [1 ]
Wu, Pengfei [2 ]
Li, Pengzhi [1 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Spine Surg, Changsha 410011, Hunan, Peoples R China
[2] Cent South Univ, Ctr Med Genet, Sch Life Sci, Changsha 410011, Hunan, Peoples R China
来源
AGING-US | 2020年 / 12卷 / 17期
基金
中国国家自然科学基金;
关键词
osteoporosis; Celastrol; BM-MSCs; PGC-1; alpha; OXIDATIVE STRESS; OBESITY; SUPPRESSION; ACTIVATION;
D O I
10.18632/aging.103590
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Celastrol has recently been identified as a prospective new treatment for obesity and several metabolic complications. However, the effect of Celastrol in osteoporosis (OP) remains unknown. In this study, we demonstrated that Celastrol promotes osteoblast differentiation and prevents adipocyte differentiation in bone marrow mesenchymal stem cells (BM-MSCs) in vitro. Mechanistically, Celastrol was able to control the differentiation of BM-MSCs by stimulating PGC-1 alpha signaling. Moreover, administration of Celastrol could alleviate bone loss and bone marrow adipose tissue (MAT) accumulation in ovariectomized (OVX) mice and aged mice. Together, these results recommended that Celastrol could regulate BM-MSCs fate and bone-fat balance in OP and skeletal aging by stimulating PGC-1 alpha, which might act as a possible therapeutic target for OP and for the prevention of skeletal aging.
引用
收藏
页码:16887 / 16898
页数:12
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