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Co-Culture of Bone Marrow Mesenchymal Stem Cell (BMSC) and Osteoclasts Regulates Cell Differentiation and Alleviates Osteoporosis by Up-Regulating miR-211
被引:1
|作者:
Yang, Shuo
[1
]
Sima, Jincheng
[1
]
Liao, Wenbo
[1
]
机构:
[1] Zunyi Med Univ, Dept Spine Surg, Affiliated Hosp, Zunyi 563003, Guizhou, Peoples R China
关键词:
Osteoclast Differentiation;
Osteoporosis;
Reactive Oxygen Species;
M-CSF;
RANKL;
RECONSTRUCTION;
D O I:
10.1166/jbt.2022.3042
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
Bone marrow mesenchymal stem cells (BMSCs) can release a large amount of exosomes (EXO) during bone remodeling by osteoclasts. EXO contains miRNA-211, which has a variety of biological effects. However, little is known about whether miR-211 from BMSC-EXO affects the surrounding cells. Therefore, we aim to study the role of miRNA-211 derived from BMSC-EXO in regulating osteoclasts differentiation. Macrophage colony stimulating factor (M-CSF) and nuclear factor kappa B receptor activator (RANKL) were used to stimulate bone marrow macrophages (BMM) to obtain osteoclasts, which were treated with BMSC-EXO or LPS followed by analysis of osteoclast-related genes expression by PCR, ROS release by flow cytometry, actin ring formation by immunofluorescence, and osteoclast differentiation by anti-tartrate acid phosphatase (TRAP) staining. Finally, an in vivo experiment was conducted to verify BMSC-EXO's effect on osteoporosis. BMSC-EXO significantly inhibited RNAKL-induced osteoclast differentiation of BMMs. During osteoclasts formation, BMSC-EXO inhibited ROS production induced by RANKL and the subsequent activation of NF-KB signaling pathway induced by ROS. In addition, BMSC-EXO significantly down-regulated the osteoclast genes including nuclear factor, cytoplasmic 1 (NFATc1), C-fos, tartrate-resistant acid IP: 182.75.148.10 On: Tue, 04 Jan 2022 11:53:03 phosphatase (TRAP) and osteoclast-associated immunoglobulin-like receptor (OSCAR) in activated Copyright: American Scientific Publishers T cells. BMSC-EXO inhibited ROS release by promoting miR-211 expression, thereby inhibiting the Delivered by Ingenta NF-KB signaling and ultimately participating in osteoclasts differentiation. In LPS-induced mouse osteoporosis models, BMSC-EXO inhibited LPS-induced bone loss and exerted a protective effect. In conclusion, microRNA-211 derived from BMSC-EXO can regulate osteoclasts differentiation, suggesting that it might be used as a potential approach for treating osteoporosis.
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页码:544 / 550
页数:7
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