Yam-derived exosome-like nanovesicles stimulate osteoblast formation and prevent osteoporosis in mice

成骨细胞 化学 运行x2 外体 骨质疏松症 细胞生物学 药理学 骨矿物 内科学 内分泌学 生物化学 生物 微泡 医学 体外 小RNA 基因
作者
Jin-Hyeon Hwang,Yu-Seong Park,Hyuk-Soon Kim,Dong-Ha Kim,Sanghoon Lee,Chan‐Hyeong Lee,Seung‐Hoon Lee,Jung‐Eun Kim,Sangkyu Lee,Ho Min Kim,Hyun‐Woo Kim,Jihoon Kim,Wonhyo Seo,Hyo‐Jung Kwon,Byoung‐Joon Song,Do‐Kyun Kim,Moon‐Chang Baek,Young‐Eun Cho
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:355: 184-198 被引量:174
标识
DOI:10.1016/j.jconrel.2023.01.071
摘要

Plants-releasing exosome-like nanovesicles (PENs) contain miRNA, bioactive lipids, mRNAs, and proteins to exert antioxidant, anti-inflammatory, and regenerative activity. Substances extracted from yams have been reported to promote osteoblast growth in bone regeneration, which prevent weak and brittle bones in osteoporosis. Herein, we describe the beneficial effects of yam-derived exosome-like nanovesicles (YNVs) on promoting differentiation and mineralization of osteoblasts for bone regeneration in ovariectomized (OVX)-induced osteoporotic mice. YNVs were successfully isolated and characterized. YNVs stimulate the proliferation, differentiation, and mineralization of osteoblasts with increased bone differentiation markers (OPN, ALP, and COLI). Interestingly, YNVs do not contain saponins including diosgenin and dioscin known to mainly exert osteogenic activity of yams. Instead, the osteogenic activity of YNVs was revealed to be resulted from activation of the BMP-2/p-p38-dependent Runx2 pathway. As a result, YNVs promote longitudinal bone growth and mineral density of the tibia in the OVX-induced osteoporotic mice in vivo, and these results positively correlate the significant increases in osteoblast-related parameters. In addition, the orally administered YNVs were transported through the GI tract and absorbed through the small intestine. These results showed an excellent systemic biosafety determined by histological analysis and liver/kidney toxicity tests. Taken together, YNVs can serve as a safe and orally effective agent in the treatment of osteoporosis.
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