骨髓炎
金黄色葡萄球菌
炎症
成骨细胞
细胞因子
医学
骨感染
免疫学
骨重建
癌症研究
微生物学
化学
生物
内科学
细菌
体外
生物化学
遗传学
作者
Chaolai Jiang,Yiwei Lin,Haojie Shan,Wenyang Xia,Chenhao Pan,Nan Wang,Lihui Zhou,Youshui Gao,Zubin Zhou,Xiaowei Yu
标识
DOI:10.1021/acsinfecdis.1c00459
摘要
Osteomyelitis is a Staphylococcus aureus-caused bone infection. In this study, the effects of miR-146a on osteomyelitis were evaluated. Using the osteoblast cell model and S. aureus-induced osteomyelitis mice model, we monitored the miR-146 expression and explored the effects of miR-146a on cell proliferation of osteoblasts, bone remodeling, osteoclastogenesis, inflammatory cytokine production, and bacterial burden. Upregulated miR-146a was found in mice with S. aureus-induced osteomyelitis. miR-146a attenuated S. aureus-induced cell loss of osteoblasts, rescued the expression of osteogenic markers, altered the bone remodeling, and inhibited inflammatory cytokine production and osteoclastogenesis. miR-146a knockout mice had higher S. aureus burden. In conclusion, miR-146a protects against S. aureus-induced osteomyelitis by regulating inflammation and osteogenesis.
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