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Abstract
Transcortical vessels (TCVs) provide effective communication between bone marrow vascular system and external circulation. Although osteocytes are in close contact with them, it is not clear whether osteocytes regulate the homeostasis of TCVs. Here, we show that osteocytes maintain the normal network of TCVs by transferring mitochondria to the endothelial cells of TCV. Partial ablation of osteocytes causes TCV regression. Inhibition of mitochondrial transfer by conditional knockout of Rhot1 in osteocytes also leads to regression of the TCV network. By contrast, acquisition of osteocyte mitochondria by endothelial cells efficiently restores endothelial dysfunction. Administration of osteocyte mitochondria resultes in acceleration of the angiogenesis and healing of the cortical bone defect. Our results provide new insights into osteocyte-TCV interactions and inspire the potential application of mitochondrial therapy for bone-related diseases.
Osteocytes are the key cellular components of cortical bone. Here they show that osteocytes transfer mitochondria to the endothelial cells of transcortical vessels (TCVs), which promotes angiogenesis and increases function of the TCV network.
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1 Shanghai Sixth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Department of Orthopaedics, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293); Shanghai Sixth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Institute of Microsurgery on Extremities, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293)
2 Shanghai Institute of Biochemistry and Cell Biology, CAS Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, University of Chinese Academy of Sciences, State Key Laboratory of Cell Biology, Shanghai, China (GRID:grid.507739.f) (ISNI:0000 0001 0061 254X)
3 The Second Affiliated Hospital of Zhejiang University School of Medicine, Department of Orthopedics, Hangzhou, China (GRID:grid.412465.0)
4 Shanghai Sixth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Department of Orthopaedics, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293)
5 Medical School, The University of Western Australia, Centre for Orthopaedic Research, Nedlands, Australia (GRID:grid.1012.2) (ISNI:0000 0004 1936 7910); Perron Institute for Neurological and Translational Science, Nedlands, Australia (GRID:grid.482226.8) (ISNI:0000 0004 0437 5686)
6 Shanxi Medical University School and Hospital of Stomatology, Shanxi Province Key Laboratory of Oral Diseases Prevention and New Materials, Taiyuan, China (GRID:grid.263452.4) (ISNI:0000 0004 1798 4018)
7 Shanghai Sixth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Department of General Surgery, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293)
8 The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Department of Orthopedics, Hangzhou, China (GRID:grid.268505.c) (ISNI:0000 0000 8744 8924)
9 Shanghai Sixth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Department of Orthopaedics, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293); Shanghai Sixth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Institute of Microsurgery on Extremities, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293); Shanghai Institute of Biochemistry and Cell Biology, CAS Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, University of Chinese Academy of Sciences, State Key Laboratory of Cell Biology, Shanghai, China (GRID:grid.507739.f) (ISNI:0000 0001 0061 254X)