Exogenous microglia enter the brain and migrate into ischaemic hippocampal lesions

被引:24
作者
Imai, F
Sawada, M
Suzuki, H
Zlokovic, BV
Kojima, J
Kuno, S
Nagatsu, T
Nitatori, T
Uchiyama, Y
Kanno, T
机构
[1] Fujita Hlth Univ, Dept Neurosurg, Aichi 4701192, Japan
[2] Japan Sci & Technol Corp, PRESTO, Kawaguchi, Saitama 3320012, Japan
[3] Fujita Hlth Univ, Inst Comprehens Med Sci, Aichi 4701192, Japan
[4] Kojima Hosp, Aichi 477003, Japan
[5] Univ So Calif, Dept Neurosurg Physiol & Biophys, Los Angelos, CA USA
[6] Iwate Med Univ, Dept Cell Biol & Neuroanat, Fac Med, Iwate, Japan
[7] Osaka Univ, Fac Med, Dept Cell Biol & Anat 1, Suita, Osaka 56500891, Japan
关键词
microglia; ischaemia; hippocampus; migration; gene therapy; drug delivery system;
D O I
10.1016/S0304-3940(99)00592-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We compared migration of systemically injected microglia into normal brain vs. ischaemic brain using a model of ischaemic hippocampal lesion. Microglia were labeled by a fluorescent dye using our standard phagocytosis procedure of microscopic particles and then injected intra-arterially into Mongolian gerbils subjected to ischaemia reperfusion neuronal injury. Delayed death of pyramidal neurons was confirmed by conventional histological analysis and dUTP nick end labeling (TUNEL) method. Clusters of dye-tagged cells migrating into the hippocampal ischaemic lesions were confirmed histochemically to be microglia. Since peripherally injected microglia exhibit specific affinity for ischaemic brain lesions and does not exacerbate ischaemic neuronal injury in the present model, we suggest that microglia may have a potential to be used as a piggy-back ride to deliver therapeutic genes and/or drugs for CNS repair following transitory global ischaemic insult. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:127 / 130
页数:4
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