SOD-Functionalized gold nanoparticles as ROS scavenger and CT contrast agent for protection and imaging tracking of mesenchymal stem cells in Idiopathic pulmonary fibrosis treatment

间充质干细胞 干细胞 移植 干细胞疗法 化学 活性氧 细胞生物学 医学 病理 癌症研究 生物医学工程 生物物理学 生物 外科
作者
Chenggong Yu,Yinjuan Lv,Xiaodi Li,Hongli Bao,Xinyue Cao,Jie Huang,Zhijun Zhang
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:459: 141603-141603 被引量:10
标识
DOI:10.1016/j.cej.2023.141603
摘要

Development of functionalized nanoplatforms to simultaneously facilitate imaging tracking of transplanted stem cells and enhance their therapeutic efficacy through weakening oxidative stress damage has been a challenge in stem cell-based therapy. Herein, superoxide dismutase (SOD)-engineered gold nanoparticles (AuNPs), [email protected] NS, was developed for collectively acting as a reactive oxygen species (ROS) scavenger and a computed tomography (CT) contrast agent for simultaneous protection and imaging tracking of mesenchymal stem cells (MSCs) in idiopathic pulmonary fibrosis (IPF) therapy. In this strategy, SOD, a key antioxidant enzyme that detoxifies intracellular ROS, was modified on the surface of AuNPs and then encapsulated into polyphosphazene nanospheres to overcome the poor cell membrane penetration and chemical stability of SOD, thereby promoting the survival of MSCs in a harsh inflammatory microenvironment by ROS elimination. What’s more, [email protected] NS where the assembly of an AuNP payload in a polyphosphazene core provides strong contrast enhancement in CT imaging owing to the dense packing of AuNP. After cellular uptake of [email protected] NS, the labeled MSCs could be detected by CT technology, achieving continuous monitoring of the distribution and migration of MSCs for 18 days after transplantation in the IPF model mouse. Furthermore, we evaluated the long-term metabolism and safety of [email protected] NS following transplantation of the stem cells into the alveolar interstitium. Consequently, this work may provide a novel insight into the development of safe and effective strategies to trace and protect transplanted stem cells, thus facilitating the subsequent preclinical research and clinical translation of stem cell-based IPF treatment.
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