共 15 条
Non-invasive imaging of GFAP expression after neuronal damage in mice
被引:85
作者:

Zhu, LY
论文数: 0 引用数: 0
h-index: 0
机构:
Xenogen Corp, Alameda, CA 94501 USA Xenogen Corp, Alameda, CA 94501 USA

Ramboz, S
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h-index: 0
机构:
Xenogen Corp, Alameda, CA 94501 USA Xenogen Corp, Alameda, CA 94501 USA

Hewitt, D
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h-index: 0
机构:
Xenogen Corp, Alameda, CA 94501 USA Xenogen Corp, Alameda, CA 94501 USA

Boring, L
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h-index: 0
机构:
Xenogen Corp, Alameda, CA 94501 USA Xenogen Corp, Alameda, CA 94501 USA

Grass, DS
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h-index: 0
机构:
Xenogen Corp, Alameda, CA 94501 USA Xenogen Corp, Alameda, CA 94501 USA

Purchio, AF
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h-index: 0
机构:
Xenogen Corp, Alameda, CA 94501 USA Xenogen Corp, Alameda, CA 94501 USA
机构:
[1] Xenogen Corp, Alameda, CA 94501 USA
关键词:
GFAP;
non-invasive biophotonic imaging;
neuronal damage;
D O I:
10.1016/j.neulet.2004.06.020
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Up-regulation of glial fibrillary acidic protein (GEAP) expression is often used as a surrogate marker of neuronal damage. We have created a transgenic mouse line that carries the luciferase gene under the transcriptional control of the mouse GFAP promoter. Biophotonic imaging was used to non-invasively detect the increase in GFAP expression after kainic acid induced neuronal cell death. We demonstrate that after kainic acid treatment, strong biophotonic signals were detected from the brain area. This correlated with both endogenous GFAP and luciferase RNA levels as well as with hippocampal cell death observed histologically. The transgenic mouse line will provide a powerful tool to dynamically monitor neuronal cell death in the living animal and will aid in the discovery and development of drugs to treat damage due to stroke and other neurodegenerative diseases. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
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页码:210 / 212
页数:3
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