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
相关论文
共 27 条
[1]   Immune reactivity in a mouse model of familial ALS correlates with disease progression [J].
Alexianu, ME ;
Kozovska, M ;
Appel, SH .
NEUROLOGY, 2001, 57 (07) :1282-1289
[2]   Role for matrix metalloproteinase 9 after focal cerebral ischemia, effects of gene knockout and enzyme inhibition with BB-94 [J].
Asahi, M ;
Asahi, K ;
Jung, JC ;
del Zoppo, GJ ;
Fini, ME ;
Lo, EH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (12) :1681-1689
[3]   Matrix metalloproteinase-9 is elevated in serum of patients with amyotrophic lateral sclerosis [J].
Beuche, W ;
Yushchenko, M ;
Mäder, M ;
Maliszewska, M ;
Felgenhauer, K ;
Weber, F .
NEUROREPORT, 2000, 11 (16) :3419-3422
[4]   Unraveling the mechanisms involved in motor neuron degeneration in ALS [J].
Bruijn, LI ;
Miller, TM ;
Cleveland, DW .
ANNUAL REVIEW OF NEUROSCIENCE, 2004, 27 :723-749
[5]   Induction of matrix metalloproteinase MMP-9 (92-kDa gelatinase) by retinoic acid in human neuroblastoma SKNBE cells:: Relevance to neuronal differentiation [J].
Chambaut-Guérin, AM ;
Hérigault, S ;
Rouet-Benzineb, P ;
Rouher, C ;
Lafuma, C .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (02) :508-517
[6]   The expression of tissue-type plasminogen activator, matrix metalloproteases and endogenous inhibitors in the central nervous system in multiple sclerosis: Comparison of stages in lesion evolution [J].
Cuzner, ML ;
Gveric, D ;
Strand, C ;
Loughlin, AJ ;
Paemen, L ;
Opdenakker, G ;
Newcombe, J .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1996, 55 (12) :1194-1204
[7]  
Dubois B, 2002, EUR J IMMUNOL, V32, P2163, DOI 10.1002/1521-4141(200208)32:8<2163::AID-IMMU2163>3.0.CO
[8]  
2-Q
[9]   Resistance of young gelatinase B-deficient mice to experimental autoimmune encephalomyelitis and necrotizing tail lesions [J].
Dubois, B ;
Masure, S ;
Hurtenbach, U ;
Paemen, L ;
Heremans, H ;
van den Oord, J ;
Sciot, R ;
Meinhardt, T ;
Hämmerling, G ;
Opdenakker, G ;
Arnold, B .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (11) :1507-1515
[10]   Gelatinase-A (MMP-2), gelatinase-B (MMP-9) and membrane type matrix metalloproteinase-1 (MT1-MMP) are involved in different aspects of the pathophysiology of malignant gliomas [J].
Forsyth, PA ;
Wong, H ;
Laing, TD ;
Rewcastle, NB ;
Morris, DG ;
Muzik, H ;
Leco, KJ ;
Johnston, RN ;
Brasher, PMA ;
Sutherland, G ;
Edwards, DR .
BRITISH JOURNAL OF CANCER, 1999, 79 (11-12) :1828-1835