微泡
间充质干细胞
骨质疏松症
骨髓
医学
干细胞
癌症研究
细胞生物学
小RNA
生物
免疫学
病理
遗传学
基因
作者
Fanying Meng,Guangchao Wang,Fengjin Zhou,Guangfeng Li,Mingkai Wang,Ziyang Zhou,Yafei Han,Xiao Chen,Yan Hu,Yuanwei Zhang,Xiuhui Wang,Yuan Chen,Zhen Geng,Jiacan Su
标识
DOI:10.1016/j.compositesb.2024.111358
摘要
Osteoporosis, increasingly prevalent among the aging population, poses a global health challenge. Current treatments, often limited by prolonged treatment durations, serious side effects, and suboptimal efficacy, necessitate innovative approaches. Building on previous research that highlighted the rejuvenating potential of young blood in organ vitality. This study focused on the role of exosomes and exosomal miRNA. Specifically, we investigated the efficacy of exosomes derived from young plasma (Y-Exos) in mitigating osteoporosis, contrasting them with exosomes from aged plasma (A-Exos). Our in vitro analysis involved co-culturing bone marrow mesenchymal stem cells (BMSCs) with Y-Exos or A-Exos, assessing their impact on BMSCs migration, proliferation, and osteogenic differentiation. Y-Exos exhibited a marked enhancement in BMSCs proliferation, migration, and osteogenic differentiation compared to A-Exos. Corresponding in vivo studies corroborated these findings, demonstrating that Y-Exos significantly alleviated osteoporosis, whereas A-Exos impeded bone regeneration. Furthermore, our research identified exosomal miR-217–5p as a pivotal contributor to the osteoprotective effects of Y-Exos. Our work provided a potential strategy for advancing the clinical treatment of osteoporosis.
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