间充质干细胞
干细胞疗法
纳米载体
干细胞
特发性肺纤维化
体内
细胞疗法
癌症研究
囊性纤维化
医学
肺
细胞
炎症
病理
免疫学
细胞生物学
生物
药理学
生物技术
药品
内科学
生物化学
作者
H. Bao,Manxiang Wu,Jie Xing,Zihou Li,Yuenan Zhang,Aiguo Wu,Juan Li
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-08-21
卷期号:10 (34)
标识
DOI:10.1126/sciadv.adq0703
摘要
Stem cell therapy is being explored as a potential treatment for idiopathic pulmonary fibrosis (IPF), but its effectiveness is hindered by factors like reactive oxygen species (ROS) and inflammation in fibrotic lungs. Moreover, the distribution, migration, and survival of transplanted stem cells are still unclear, impeding the clinical advancement of stem cell therapy. To tackle these challenges, we fabricate AuPtCoPS trimetallic-based nanocarriers (TBNCs), with enzyme-like activity and plasmid loading capabilities, aiming to efficiently eradicate ROS, facilitate delivery of therapeutic genes, and ultimately improve the therapeutic efficacy. TBNCs also function as a computed tomography contrast agent for tracking mesenchymal stem cells (MSCs) during therapy. Accordingly, we enhanced the antioxidant stress and anti-inflammatory capabilities of engineered MSCs and successfully visualized their biological behavior in IPF mice in vivo. Overall, this study provides an efficient and forward-looking treatment approach for IPF and establishes a framework for a stem cell–based therapeutic system aimed at addressing lung disease.
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