牙髓干细胞
破骨细胞
炎症
肿瘤坏死因子α
脂多糖
化学
细胞生物学
小RNA
癌症研究
刺激
再生(生物学)
骨愈合
干细胞
医学
免疫学
受体
内科学
解剖
生物
生物化学
基因
作者
Jiakang Yang,Jing Shuai,Lixuen Siow,Jingyi Lu,Miao Sun,Wenyue An,Mengfei Yu,Baixiang Wang,Qianming Chen
出处
期刊:Bone research
[Springer Nature]
日期:2024-01-14
卷期号:12 (1): 2-2
被引量:30
标识
DOI:10.1038/s41413-023-00299-0
摘要
Abstract Reconstruction of irregular oral-maxillofacial bone defects with an inflammatory microenvironment remains a challenge, as chronic local inflammation can largely impair bone healing. Here, we used magnesium silicate nanospheres (MSNs) to load microRNA-146a-5p (miR-146a) to fabricate a nanobiomaterial, MSN+miR-146a, which showed synergistic promoting effects on the osteogenic differentiation of human dental pulp stem cells (hDPSCs). In addition, miR-146a exhibited an anti-inflammatory effect on mouse bone marrow-derived macrophages (BMMs) under lipopolysaccharide (LPS) stimulation by inhibiting the NF-κB pathway via targeting tumor necrosis factor receptor-associated factor 6 (TRAF6), and MSNs could simultaneously promote M2 polarization of BMMs. MiR-146a was also found to inhibit osteoclast formation. Finally, the dual osteogenic-promoting and immunoregulatory effects of MSN+miR-146a were further validated in a stimulated infected mouse mandibular bone defect model via delivery by a photocuring hydrogel. Collectively, the MSN+miR-146a complex revealed good potential in treating inflammatory irregular oral-maxillofacial bone defects.
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