Role of matrix metalloproteinase-9 in a mouse model for amyotrophic lateral sclerosis

被引:25
|
作者
Dewil, M
Schurmans, C
Starckx, S
Opdenakker, G
Van Den Bosch, L
Robberecht, W
机构
[1] Univ Leuven, Neurobiol Lab, B-3000 Louvain, Belgium
[2] Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
关键词
amyotrophic lateral sclerosis; glia; inflammation; matrix metalloproteinase-9; microglia; motor neuron;
D O I
10.1097/00001756-200503150-00003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The pathogenesis of amyotrophic lateral sclerosis remains poorly understood, but microglial and astroglial activation are thought to contribute to motor neuron death. Evidence suggests that matrix metalloproteinase-9 (MMP-9) is a mediator of this deleterious effect. In this study, we evaluated the effect of MMP-9 on the pathogenesis of amyotrophic lateral sclerosis. Although marked microglial and astroglial proliferation was seen in the spinal cord and in-vitro studies proved MMP-9 to be produced by these cells, deletion of the MMP-9 gene in SODIG93A mice accelerated rather than delayed the motor neuron disease and significantly reduced survival. Our results suggest that the effect of MMP-9 on mutant superoxide dismutase-I (SODI)-induced motor neuron disease is protective rather than hazardous. Therefore, the effect of pharmacological inhibition of MMP-9 activity is unlikely to be of therapeutical benefit in amyotrophic lateral sclerosis. NeuroReport 16:321-324 (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:321 / 324
页数:4
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