材料科学
归巢(生物学)
间充质干细胞
大脑
冲程(发动机)
癌症研究
医学
生物医学工程
内科学
细胞生物学
中枢神经系统
生物
生态学
机械工程
工程类
作者
Tianyuan Zhang,Fangyuan Li,Qianhao Xu,Qiyue Wang,Xinchi Jiang,Zeyu Liang,Hongwei Liao,Xianglei Kong,Jianan Liu,Honghui Wu,Danping Zhang,Changhua An,Liang Dong,Yang Lü,Hongcui Cao,Dokyoon Kim,Jihong Sun,Taeghwan Hyeon,Jianqing Gao,Daishun Ling
标识
DOI:10.1002/adfm.201900603
摘要
Abstract Unsatisfactory post‐stroke recovery has long been a negative factor in the prognosis of ischemic stroke due to the lack of pharmacological treatments. Mesenchymal stem cells (MSCs)‐based therapy has recently emerged as a promising strategy redefining stroke treatment; however, its effectiveness has been largely restricted by insufficient therapeutic gene expression and inadequate cell numbers in the ischemic cerebrum. Herein, a non‐viral and magnetic field‐independent gene transfection approach is reported, using magnetosome‐like ferrimagnetic iron oxide nanochains (MFIONs), to genetically engineer MSCs for highly efficient post‐stroke recovery. The 1D MFIONs show efficient cellular uptake by MSCs, which results in highly efficient genetic engineering of MSCs to overexpress brain‐derived neurotrophic factor for treating ischemic cerebrum. Moreover, the internalized MFIONs promote the homing of MSCs to the ischemic cerebrum by upregulating CXCR4. Consequently, a pronounced recovery from ischemic stroke is achieved using MFION‐engineered MSCs in a mouse model.
科研通智能强力驱动
Strongly Powered by AbleSci AI