Matrix metalloproteinases and their endogenous inhibitors in neuronal physiology of the adult brain

被引:245
作者
Dzwonek, J
Rylski, M
Kaczmarek, L
机构
[1] M Nencki Inst Expt Biol, Dept Mol & Cellular Neurobiol, PL-02093 Warsaw, Poland
[2] Univ Warmia & Mazury, Fac Biol, Dept Genet, PL-10719 Olsztyn, Poland
关键词
brain; neuron; neuronal plasticity; long term potentiation; memory matrix metalloproteinase-9;
D O I
10.1016/j.febslet.2004.03.070
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
More than 20 matrix metalloproteinases (MMPs) and four of their endogenous tissue inhibitors (TIMPs) act together to control tightly temporally restricted, focal proteolysis of extracellular matrix. In the neurons of the adult brain several components of the TIMP/MMP system are expressed and are responsive to changes in neuronal activity. Futhermore, functional studies, especially involving blocking of MMP activites, along with the identification of MMP substrates in the brain strongly suggest that this enzymatic system plays an important physiological role in adult brain neurons, possibly being pivotal for neuronal plasticity. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 135
页数:7
相关论文
共 80 条
[1]   Nitric oxide increases the decay of matrix metalloproteinase 9 mRNA by inhibiting the expression of mRNA-stabilizing factor HuR [J].
Akool, ES ;
Kleinert, H ;
Hamada, FMA ;
Abdelwahab, MH ;
Förstermann, U ;
Pfeilschifter, J ;
Eberhardt, W .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (14) :4901-4916
[2]   Matrix metalloproteinase expression in an experimentally-induced DTH model of multiple sclerosis in the rat CNS [J].
Anthony, DC ;
Miller, KM ;
Fearn, S ;
Townsend, MJ ;
Opdenakker, G ;
Wells, GMA ;
Clements, JM ;
Chandler, S ;
Gearing, AJH ;
Perry, VH .
JOURNAL OF NEUROIMMUNOLOGY, 1998, 87 (1-2) :62-72
[3]   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
[4]   Matrix metalloproteinase 2 gene knockout has no effect on acute brain injury after focal ischemia [J].
Asahi, M ;
Sumii, T ;
Fini, ME ;
Itohara, S ;
Lo, EH .
NEUROREPORT, 2001, 12 (13) :3003-3007
[5]  
Asahina M, 2001, CLIN NEUROPATHOL, V20, P60
[6]   CHARACTERIZATION OF NEUTRAL PROTEINASES FROM ALZHEIMER-AFFECTED AND CONTROL BRAIN SPECIMENS - IDENTIFICATION OF CALCIUM-DEPENDENT METALLOPROTEINASES FROM THE HIPPOCAMPUS [J].
BACKSTROM, JR ;
MILLER, CA ;
TOKES, ZA .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (03) :983-992
[7]  
Backstrom JR, 1996, J NEUROSCI, V16, P7910
[8]   Plasminogen activators and matrix metalloproteases, mediators of extracellular proteolysis in inflammatory demyelination of the central nervous system [J].
Cuzner, ML ;
Opdenakker, G .
JOURNAL OF NEUROIMMUNOLOGY, 1999, 94 (1-2) :1-14
[9]   Inflammatory genes are upregulated in expanded ataxin-3-expressing cell lines and spinocerebellar ataxia type 3 brains [J].
Evert, BO ;
Vogt, IR ;
Kindermann, C ;
Ozimek, L ;
de Vos, RAI ;
Brunt, ERP ;
Schmitt, I ;
Klockgether, T ;
Wüllner, U .
JOURNAL OF NEUROSCIENCE, 2001, 21 (15) :5389-5396
[10]   Differential spatial distribution and temporal regulation of tissue inhibitor of metalloproteinase mRNA expression during rat central nervous system development [J].
Fager, N ;
Jaworski, DM .
MECHANISMS OF DEVELOPMENT, 2000, 98 (1-2) :105-109