线粒体
破骨细胞
细胞生物学
骨吸收
髓样
平衡
糖皮质激素
化学
生物
免疫学
癌症研究
内分泌学
生物化学
体外
作者
Peng Ding,Chuan Gao,Jian Zhou,Jialun Mei,Li Gan,Delin Liu,Hao Li,Peng Liao,Yao Meng,Bingqi Wang,Yafei Lu,Xiaoyuan Peng,Chenyi Jiang,Jimin Yin,Yigang Huang,Minghao Zheng,Youshui Gao,Changqing Zhang,Junjie Gao
标识
DOI:10.1038/s41467-024-49159-3
摘要
Abstract Interactions between osteolineage cells and myeloid cells play important roles in maintaining skeletal homeostasis. Herein, we find that osteolineage cells transfer mitochondria to myeloid cells. Impairment of the transfer of mitochondria by deleting MIRO1 in osteolineage cells leads to increased myeloid cell commitment toward osteoclastic lineage cells and promotes bone resorption. In detail, impaired mitochondrial transfer from osteolineage cells alters glutathione metabolism and protects osteoclastic lineage cells from ferroptosis, thus promoting osteoclast activities. Furthermore, mitochondrial transfer from osteolineage cells to myeloid cells is involved in the regulation of glucocorticoid-induced osteoporosis, and glutathione depletion alleviates the progression of glucocorticoid-induced osteoporosis. These findings reveal an unappreciated mechanism underlying the interaction between osteolineage cells and myeloid cells to regulate skeletal metabolic homeostasis and provide insights into glucocorticoid-induced osteoporosis progression.
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