Huang Qing, Jiang Yang, Cao Yang, Ding Yunchuan, Cai Jinghui, Yang Tingqian, Zhou Xin, Wu Qiang, Li Danyang, Liu Qingyu, Li Fangping
Department of Endocrinology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen 518107, China.
Research Center, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen 518107, China.
Regen Biomater. 2024 Sep 13;11:rbae112. doi: 10.1093/rb/rbae112. eCollection 2024.
The imbalance between osteoblasts and osteoclasts is the cause of osteoporosis. Milk-derived extracellular vesicles (mEVs), excellent drug delivery nanocarriers, can promote bone formation and inhibit bone resorption. In this study, we conjugated bone-targeting peptide (AspSerSer, DSS) to mEVs by click chemistry and then loaded with SRT2104, a SIRT1 (silent mating-type information regulation 2 homolog 1) agonist that was proofed to help reduce bone loss. The engineered (DSS)-mEV-SRT2104 had the intrinsic anti-osteoporosis function of mEVs and SRT2104 to reverse the imbalance in bone homeostasis by simultaneously regulating osteogenesis and osteoclastogenesis. Furthermore, we labelled mEVs with MnB nanoparticles that can be used for the magnetic resonance imaging (MRI) visualization. The obtained nanocomposites significantly prevented bone loss in osteoporosis mice and increased bone mineral density, exhibiting superior bone accumulation under MRI. We believe the proposed (DSS)-mEV-SRT2104/MnB provides a novel paradigm for osteoporosis treatment and monitoring.
成骨细胞与破骨细胞之间的失衡是骨质疏松症的病因。源自牛奶的细胞外囊泡(mEVs)是出色的药物递送纳米载体,可促进骨形成并抑制骨吸收。在本研究中,我们通过点击化学将骨靶向肽(天冬氨酸丝氨酸丝氨酸,DSS)与mEVs偶联,然后装载SRT2104,这是一种SIRT1(沉默交配型信息调节2同源物1)激动剂,已被证明有助于减少骨质流失。工程化的(DSS)-mEV-SRT2104具有mEVs和SRT2104的内在抗骨质疏松功能,通过同时调节成骨作用和破骨细胞生成来逆转骨稳态的失衡。此外,我们用可用于磁共振成像(MRI)可视化的MnB纳米颗粒标记mEVs。所获得的纳米复合材料显著预防了骨质疏松症小鼠的骨质流失并增加了骨矿物质密度,在MRI下表现出优异的骨蓄积。我们相信所提出的(DSS)-mEV-SRT2104/MnB为骨质疏松症的治疗和监测提供了一种新的范例。