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

Authors
Zhang, TianyuanLi, FangyuanXu, QianhaoWang, QiyueJiang, XinchiLiang, ZeyuLiao, HongweiKong, XiangleiLiu, JiananWu, HonghuiZhang, DanpingAn, ChanghuaDong, LiangLu, YangCao, HongcuiKim, DokyoonSun, JihongHyeon, TaeghwanGao, JianqingLing, Daishun
Issue Date
Jun-2019
Publisher
John Wiley & Sons Ltd.
Keywords
ferrimagnetic iron oxide nanochains; genetic engineering; ischemic cerebrum homing; mesenchymal stem cells; post-stroke recovery
Citation
Advanced Functional Materials, v.29, no.24, pp.1 - 13
Indexed
SCIE
SCOPUS
Journal Title
Advanced Functional Materials
Volume
29
Number
24
Start Page
1
End Page
13
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/2903
DOI
10.1002/adfm.201900603
ISSN
1616-301X
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.
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ERICA 첨단융합대학 (ERICA 바이오나노공학전공)
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