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Ferrimagnetic Nanochains-Based Mesenchymal Stem Cell Engineering for Highly Efficient Post-Stroke Recovery

Cited 64 time in Web of Science Cited 68 time in Scopus
Authors

Zhang, Tianyuan; Li, Fangyuan; Xu, Qianhao; Wang, Qiyue; Jiang, Xinchi; Liang, Zeyu; Liao, Hongwei; Kong, Xianglei; Liu, Jianan; Wu, Honghui; Zhang, Danping; An, Changhua; Dong, Liang; Lu, Yang; Cao, Hongcui; Kim, Dokyoon; Sun, Jihong; Hyeon, Taeghwan; Gao, Jianqing; Ling, Daishun

Issue Date
2019-06
Publisher
John Wiley & Sons Ltd.
Citation
Advanced Functional Materials, Vol.29 No.24, p. 1900603
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.
ISSN
1616-301X
URI
https://hdl.handle.net/10371/165774
DOI
https://doi.org/10.1002/adfm.201900603
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Chemistry, Materials Science

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