Biomimetic Prussian blue nanozymes with enhanced bone marrow-targeting for treatment of radiation-induced hematopoietic injury

被引:24
作者
Zhang, Bowen [1 ,3 ]
Chen, Gan [2 ]
Wu, Xumin [1 ,3 ]
Li, Yunxing [1 ]
Xiao, Yao [2 ]
Li, Jisheng [1 ]
He, Lijuan [2 ,3 ]
Li, Yunqiao [1 ]
Wang, Sihan [1 ,3 ]
Zhao, Jiahui [1 ]
Liu, Chuanli [1 ]
Zhou, Hong [2 ]
Li, Yanhua [1 ,3 ]
Pei, Xuetao [1 ,3 ]
机构
[1] Beijing Inst Radiat Med, Beijing 100850, Peoples R China
[2] Inst Hlth Serv & Transfus Med, Beijing 100850, Peoples R China
[3] South China Res Ctr Stem Cell & Regenerat Med, SCIB, Guangzhou 510005, Peoples R China
基金
中国国家自然科学基金;
关键词
Prussian blue nanozymes; Mesenchymal stem cell membrane; Reactive oxygen species; Radiation-induced hematopoietic injury; Targeting therapy; MESENCHYMAL STEM-CELLS; IONIZING-RADIATION; CATALASE; NANOPARTICLES; REGENERATION; GENERATION; INCREASES; MIGRATION; THERAPY; DAMAGE;
D O I
10.1016/j.biomaterials.2022.121980
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There is an urgent medical need to develop effective therapies that can ameliorate damage to the radiation -exposed hematopoietic system. Nanozymes with robust antioxidant properties have a therapeutic potential for mitigating radiation-induced hematopoietic injury. However, enhancing nanozyme recruitment to injured tissues in vivo while maintaining their catalytic activity remains a great challenge. Herein, we present the design and preparation of a biomimetic nanoparticle, a mesenchymal stem cell membrane camouflaged Prussian blue nanozyme (PB@MSCM), which exhibits biocompatible surface properties and demonstrates enhanced injury site -targeting towards the irradiated murine bone marrow niche. Notably, the constructed PB@MSCM possessed redox enzyme-mimic catalytic activity and could scavenge overproduced reactive oxygen species in the irradi-ated bone marrow cells, both in vitro and ex vivo. More importantly, the administration of PB@MSCM signifi-cantly mitigated hematopoietic cell apoptosis and accelerated the regeneration of hematopoietic stem and progenitor cells. Our findings provide a new targeted strategy to improve nanozyme therapy in vivo and mitigate radiation-induced hematopoietic injury.
引用
收藏
页数:17
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