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

  • Biomaterials. 2023 Feb:293:121980. doi: 10.1016/j.biomaterials.2022.121980.
Bowen Zhang  1 Gan Chen  2 Xumin Wu  1 Yunxing Li  3 Yao Xiao  2 Jisheng Li  3 Lijuan He  4 Yunqiao Li  3 Sihan Wang  1 Jiahui Zhao  3 Chuanli Liu  3 Hong Zhou  5 Yanhua Li  6 Xuetao Pei  7
Affiliations
  • 1. Beijing Institute of Radiation Medicine, Beijing 100850, China; South China Research Center for Stem Cell & Regenerative Medicine, SCIB, Guangzhou 510005, China.
  • 2. Institute of Health Service and Transfusion Medicine, Beijing 100850, China.
  • 3. Beijing Institute of Radiation Medicine, Beijing 100850, China.
  • 4. Institute of Health Service and Transfusion Medicine, Beijing 100850, China; South China Research Center for Stem Cell & Regenerative Medicine, SCIB, Guangzhou 510005, China.
  • 5. Institute of Health Service and Transfusion Medicine, Beijing 100850, China. Electronic address: [email protected].
  • 6. Beijing Institute of Radiation Medicine, Beijing 100850, China; South China Research Center for Stem Cell & Regenerative Medicine, SCIB, Guangzhou 510005, China. Electronic address: [email protected].
  • 7. Beijing Institute of Radiation Medicine, Beijing 100850, China; South China Research Center for Stem Cell & Regenerative Medicine, SCIB, Guangzhou 510005, China. Electronic address: [email protected].
Abstract

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 irradiated bone marrow cells, both in vitro and ex vivo. More importantly, the administration of PB@MSCM significantly 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.

Keywords
Mesenchymal stem cell membrane; Prussian blue nanozymes; Radiation-induced hematopoietic injury; Reactive oxygen species; Targeting therapy.