Treatment of hypoxic-ischemic encephalopathy in mouse by transplantation of embryonic stem cell-derived cells

被引:30
作者
Ma, Jie [1 ]
Wang, Yu
Yang, Jianhua
Yang, Min
Chang, Keun-A
Zhang, Linhua
Jiang, Feng
Li, Yi
Zhang, Zhonggong
Heo, Chaejeong
Suh, Yoo-Hun
机构
[1] Shanghai Jiao Tong Univ, Dept Pediat Neurosurg, Xinhua Hosp, Shanghai 200092, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Neurol Surg, Xinhua Hosp, Shanghai 200092, Peoples R China
[3] Seoul Natl Univ, Dept Pharmacol, Coll Med, Natl Creat Res Initiat Ctr Alzheimers Dementia, Seoul 110799, South Korea
[4] Seoul Natl Univ, MRC, Neurosci Res Inst, Seoul 110799, South Korea
[5] Natl Res Council Canada, Biotechnol Res Inst, Montreal, PQ H4P 2R2, Canada
基金
中国国家自然科学基金;
关键词
hypoxic-ischemic encephalopathy; embryonic neural stem cell; neonatal mouse; cells transplantation;
D O I
10.1016/j.neuint.2007.04.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A 7-day-old hypoxic-ischemic encephalopathy (HIE) mouse model was used to study the effect of transplantation of embryonic stem (ES) cell-derived cells on the HIE. After the inducement in vitro, the ES cell-derived cells expressed Nestin and MAP-2, rather than GFAP mRNA. After transplantation, ES cell-derived cells can survive, migrate into the injury site, and specifically differentiate into neurons, showing improvement of the learning ability and memory of the HIE mouse at 8 months post-transplantation. The non-grafted HIE mouse brain showed typical patholo gical changes in the hippocampus and cerebral cortex, where the number of neurons was reduced, while in the cell graft group, number of the neurons increased in the same regions. Although further study is necessary to elucidate the precise mechanisms responsible for this functional recovery, we believe that ES cells have advantages for use as a donor source in HIE. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:57 / 65
页数:9
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