Early increase of apoptosis-linked gene-2 interacting protein X in areas of kainate-induced neurodegeneration

被引:25
作者
Hemming, FJ [1 ]
Fraboulet, S [1 ]
Blot, B [1 ]
Sadoul, R [1 ]
机构
[1] Univ Grenoble 1, INSERM, Hop A Michallon, EMI 0108,CHU, F-38043 Grenoble 9, France
关键词
cell death; epilepsy; ALG-2; synapse; hippocampus; piriform cortex;
D O I
10.1016/j.neuroscience.2003.10.036
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Apoptosis-linked gene-2 interacting protein X (Alix) is thought to be involved in both cell death and vesicular trafficking. We examined Alix expression 2 h, 6 h and 24 h after triggering seizure-dependent neuronal death by i.p. kainic acid injection. In the hippocampus, intense, transient immunolabelling was observed in the strata lucidum, oriens and radiatum, areas of high synaptic activity. The similarity of this distribution to those of synaptophysin and endophilin suggests a presynaptic localisation. Alix labelling was increased in neuronal cell bodies in kainate-sensitive regions before or concomitant with the first signs of oedema and/or neuronal eosinophilia. The increase persisted 24 h after kainate-injection in CA3 and the piriform cortex which are areas with massive swelling and numerous pyknotic neurons. This suggests that Alix may play an early role in the mechanisms leading to cell death. Taken together, our results suggest that Alix may be a molecular link between synaptic functioning and neuronal death. (C) 2004 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:887 / 895
页数:9
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