微泡
小RNA
外体
再生(生物学)
细胞生物学
破骨细胞
自愈水凝胶
再生医学
骨髓
癌症研究
翻译(生物学)
骨组织
间充质干细胞
生物
干细胞
组织工程
细胞
材料科学
生物医学工程
RNA干扰
遗传增强
骨愈合
成骨细胞
骨吸收
基因表达
细胞外小泡
胞外囊泡
生长因子
骨髓干细胞
细胞生长
细胞分化
基因
作者
Haizhu Kuang,Jing Ma,Xinyu Chi,Qichen Fu,Qianzhe Zhu,Weiling Cao,Peng Zhang,Xin Xie
标识
DOI:10.1021/acsami.2c21933
摘要
MicroRNAs (miRNAs) are a new therapeutic tool that can target multiple genes by inducing translation repression and target mRNA degradation. Although miRNAs have gained significant attention in oncology and in work on genetic disorders and autoimmune diseases, their application in tissue regeneration remains hindered by several challenges, such as miRNA degradation. Here, we reported Exosome@MicroRNA-26a (Exo@miR-26a), an osteoinductive factor that can be substituted for routinely used growth factors, which was constructed using bone marrow stem cell (BMSC)-derived exosomes and microRNA-26a (miR-26a). Exo@miR-26a-integrated hydrogels significantly promoted bone regeneration when implanted into defect sites; as the exosome stimulated angiogenesis, miR-26a promoted osteogenesis while the hydrogel enabled a site-directed release. Moreover, BMSC-derived exosomes further facilitated healthy bone regeneration by repressing osteoclast differentiation-related genes rather than damaging osteoclasts. Taken together, our findings demonstrate the promising potential of Exo@miR-26a for bone regeneration and provide a new strategy for the application of miRNA therapy in tissue engineering.
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