Autologous transplantation of expanded neural precursor cells into the demyelinated monkey spinal cord

被引:37
|
作者
Oka, S
Honmou, O
Akiyama, Y
Sasaki, M
Houkin, K
Hashi, K
Kocsis, JD
机构
[1] Sapporo Med Univ, Sch Med, Dept Neurosurg, Chuo Ku, Sapporo, Hokkaido 0608543, Japan
[2] Yale Univ, Sch Med, Dept Neurol, West Haven, CT 06516 USA
[3] VA Connecticut Healthcare Syst, Neurosci Res Ctr, West Haven, CT 06516 USA
关键词
axon; demyelination; glia; myelin; multiple sclerosis; neural stem cell;
D O I
10.1016/j.brainres.2004.09.062
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The objective of this study was to establish if neural precursor cells could safely be developed from biopsy of the subventricular zone (SVZ) in the non-human primate (marmoset), and to determine their myelinating potential after autologous transplantation into a demyelinated lesion. Small amounts of tissue were safely collected from the subventricular-subependymal zone of the adult primate brain under ultrasonography without any neurological deficit. Neural precursor cells were isolated and expanded in the presence of mitogen in vitro. The dorsal columns of the adult marmoset spinal cord were demyelinated by X-irradiation and intraspinal injections of ethidium bromide in the center of the radiation field. Cell suspensions of the neural precursors were microinjected through a micropipette into the demyelinated lesion site in the spinal cord. Lesions were histologically examined 3 weeks after transplantation. Light and electron microscopic examination of plastic embedded sections revealed a significant number of myelinating profiles in the transplantation zone; no myelination was observed in control lesions. The myelinated axons had predominantly peripheral patterns of myelination. These results demonstrate that autologous transplantation of neural precursor cells in the adult nonhuman primate can remyelinate demyelinated central nervous system (CNS) axons, thus suggesting the potential utility of such an approach in demyelinating lesions in humans. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 102
页数:9
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