Time-dependent contribution of non neuronal cells to BDNF production after ischemic stroke in rats

被引:120
作者
Bejot, Yannick [1 ,2 ,3 ,4 ]
Prigent-Tessier, Anne [1 ,2 ]
Cachia, Claire [2 ]
Giroud, Maurice [2 ,3 ,4 ]
Mossiat, Claude [1 ,2 ]
Bertrand, Nathalie [1 ,2 ]
Garnier, Philippe [1 ,2 ]
Marie, Christine [1 ,2 ]
机构
[1] INSERM, Motricite Plasticite U887, Fac Pharm, F-21078 Dijon, France
[2] Univ Bourgogne, F-21079 Dijon, France
[3] Univ Hosp, Dept Neurol, F-21000 Dijon, France
[4] Ctr Epidemiol Populat, EA4184, F-21000 Dijon, France
关键词
BDNF localization; BDNF production; Stroke; Brain ischemia; Rats; CEREBRAL-ARTERY OCCLUSION; RETROGRADE AXONAL-TRANSPORT; MESSENGER-RNA EXPRESSION; NEUROTROPHIC FACTOR BDNF; ENDOTHELIAL-CELLS; CHOROID-PLEXUS; NEUROPROTECTIVE ROLE; FOCAL ISCHEMIA; BRAIN-INJURY; PLASTICITY;
D O I
10.1016/j.neuint.2010.10.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Although brain-derived neurotrophic factor (BDNF) plays a central role in recovery after cerebral ischemia, little is known about cells involved in BDNF production after stroke. The present study testes the hypothesis that neurons are not the unique source of neosynthesized BDNF after stroke and that non neuronal-BDNF producing cells differ according to the delay after stroke induction. For this purpose, cellular localization of BDNF and BDNF content of each hemisphere were analysed in parallel before and after (4 h, 24 h and 8 d) ischemic stroke in rats. Stroke of different seventies was induced by embolization of the brain with variable number of calibrated microspheres allowing us to explore the association between BDNF production and neuronal death severity. The main results are that (a) unilateral stroke increased BDNF production in both hemispheres with a more intense and long-lasting effect in the lesioned hemisphere, (b) BDNF levels either of the lesioned or unlesioned hemispheres were not inversely correlated to neuronal death severity whatever the delay after stroke onset, (c) in the unlesioned hemisphere, stroke resulted in increased BDNF staining in neurons and ependymal cells (at 4 h and 24 h), (d) in the lesioned hemisphere, beside neurons and ependymal cells, microglial cells (at 24 h), endothelial cells of cerebral arterioles (at 4 h and 24 h) and astrocytes (at 8 d) exhibited a robust BDNF staining as well. Taken together, overall data suggest that non neuronal cells are able to produce substantial amount of BDNF after ischemic stroke and that more attention should be given to these cells in the design of strategies aimed at improving stroke recovery through BDNF-related mechanisms. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:102 / 111
页数:10
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