Mapping transplanted stem cell migration after a stroke: a serial, in vivo magnetic resonance imaging study

被引:204
作者
Modo, M
Mellodew, K
Cash, D
Fraser, SE
Meade, TJ
Price, J
Williams, SCR
机构
[1] Kings Coll London, Inst Psychiat, Neuroimaging Res Grp Neurol P042, London SE5 8AF, England
[2] Kings Coll London, Inst Psychiat, Dept Neurosci, London SE5 8AF, England
[3] CALTECH, Beckman Inst, Pasadena, CA 91195 USA
[4] Northwestern Univ, Dept Chem, Chicago, IL 60208 USA
[5] Northwestern Univ, Dept Biochem, Chicago, IL 60208 USA
[6] Northwestern Univ, Dept Mol & Cell Biol, Chicago, IL 60208 USA
[7] Northwestern Univ, Dept Neurobiol, Chicago, IL 60208 USA
[8] Northwestern Univ, Dept Physiol, Chicago, IL 60208 USA
基金
英国医学研究理事会;
关键词
MCAo; neural stem cells; migration; contrast agent; cell tracking; neural transplants; MRI;
D O I
10.1016/j.neuroimage.2003.08.030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Preferential migration of stem cells toward the site of a lesion is a highly desirable property of stem cells that allows flexibility in the site of graft implantation in the damaged brain. In rats with unilateral stroke damage, neural stem cells transplanted into the contralateral hemisphere migrate across to the lesioned hemisphere and populate the area around the ischaemic infarct. To date, the migration of neural stem cells in the damaged brain has been mainly inferred from snapshot histological images. In this study, we demonstrate that by pre-labelling neural stem cells with the bimodal contrast agent Gadolinium-Rhodamine Dextran [GRID, detectable by both magnetic resonance imaging (MRI) and fluorescent microscopy], the transhemispheric migration of transplanted neural stem cells contralateral to a stroke lesion can be followed in vivo by serial MM and corroborated by subsequent histological analyses. Our results indicate that neural stem cells migrated from the injection tract mainly along the corpus callosum within 7 days of transplantation and extensively re-populated the peri-lesion area by 14 days following implantation. In contrast, neural stem cells transplanted into sham controls did not show any substantial migration outside of the injection tract, suggesting that the transcellosal migration observed in the stroke-lesioned animals is due to neural stem cells being attracted by the lesion site. In vivo tracking of the migration of neural stem cells responding to damage will greatly enhance our understanding of optimal transplantation strategies as well as how neural stem cells promote functional and anatomical recovery in neurological disorders. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:311 / 317
页数:7
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