Matrix metalloproteinase-9 involvement in the structural plasticity of dendritic spines

被引:64
|
作者
Stawarski, Michal [1 ]
Stefaniuk, Marzena [2 ]
Wlodarczyk, Jakub [1 ]
机构
[1] M Nencki Inst Expt Biol, Dept Mol & Cellular Neurobiol, Lab Cell Biophys, PL-02093 Warsaw, Poland
[2] M Nencki Inst Expt Biol, Dept Mol & Cellular Neurobiol, Neurobiol Lab, PL-02093 Warsaw, Poland
来源
FRONTIERS IN NEUROANATOMY | 2014年 / 8卷
关键词
matrix metalloproteinase-9; dendritic spines; structural synaptic plasticity; extracellular matrix; epilepsy; LONG-TERM POTENTIATION; MATRIX-METALLOPROTEINASE ACTIVITY; FRAGILE-X-SYNDROME; RESPONSE MEDIATOR PROTEIN-2; EXTRACELLULAR-MATRIX; TISSUE INHIBITOR; GENE-EXPRESSION; NMDA RECEPTORS; GELATINASE-B; SYNAPTIC STRUCTURES;
D O I
10.3389/fnana.2014.00068
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Dendritic spines are the locus for excitatory synaptic transmission in the brain and thus play a major role in neuronal plasticity. The ability to alter synaptic connections includes volumetric changes in dendritic spines that are driven by scaffolds created by the extracellular matrix (ECM). Here, we review the effects of the proteolytic activity of ECM proteases in physiological and pathological structural plasticity. We use matrix metalloproteinase-9 (MMP-9) as an example of an ECM modifier that has recently emerged as a key molecule in regulating the morphology and dysmorphology of dendritic spines that underlie synaptic plasticity and neurological disorders, respectively. We summarize the influence of MMP-9 on the dynamic remodeling of the ECM via the cleavage of extracellular substrates. We discuss its role in the formation, modification, and maintenance of dendritic spines in learning and memory. Finally, we review research that implicates MMP-9 in aberrant synaptic plasticity and spine dysmorphology in neurological disorders, with a focus on morphological abnormalities of dendritic protrusions that are associated with epilepsy.
引用
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页数:15
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