MMPs in learning and memory and neuropsychiatric disorders

被引:161
作者
Beroun, Anna [1 ]
Mitra, Shiladitya [1 ]
Michaluk, Piotr [1 ]
Pijet, Barbara [1 ]
Stefaniuk, Marzena [1 ]
Kaczmarek, Leszek [1 ]
机构
[1] Nencki Inst, BRAINCITY, Pasteura 3, PL-02093 Warsaw, Poland
关键词
Behavioral training; Schizophrenia; Autism; Epilepsy; Addiction; LONG-TERM POTENTIATION; MATRIX-METALLOPROTEINASE ACTIVITY; TRAUMATIC BRAIN-INJURY; CENTRAL-NERVOUS-SYSTEM; FRAGILE-X-SYNDROME; INDUCED BEHAVIORAL SENSITIZATION; NEUROTROPHIC FACTOR BDNF; TUMOR-CELL MIGRATION; TISSUE INHIBITOR; MATRIX-METALLOPROTEINASE-9; MMP-9;
D O I
10.1007/s00018-019-03180-8
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
Matrix metalloproteinases (MMPs) are a group of over twenty proteases, operating chiefly extracellularly to cleave components of the extracellular matrix, cell adhesion molecules as well as cytokines and growth factors. By virtue of their expression and activity patterns in animal models and clinical investigations, as well as functional studies with gene knockouts and enzyme inhibitors, MMPs have been demonstrated to play a paramount role in many physiological and pathological processes in the brain. In particular, they have been shown to influence learning and memory processes, as well as major neuropsychiatric disorders such as schizophrenia, various kinds of addiction, epilepsy, fragile X syndrome, and depression. A possible link connecting all those conditions is either physiological or aberrant synaptic plasticity where some MMPs, e.g., MMP-9, have been demonstrated to contribute to the structural and functional reorganization of excitatory synapses that are located on dendritic spines. Another common theme linking the aforementioned pathological conditions is neuroinflammation and MMPs have also been shown to be important mediators of immune responses.
引用
收藏
页码:3207 / 3228
页数:22
相关论文
共 269 条
[11]  
[Anonymous], 2013, Investing in Mental Health
[12]   Differential matrix metalloproteinase expression in cases of multiple sclerosis and stroke [J].
Anthony, DC ;
Ferguson, B ;
Matyzak, MK ;
Miller, KM ;
Esiri, MM ;
Perry, VH .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1997, 23 (05) :406-415
[13]   Early postnatal expression and localization of matrix metalloproteinases-2 and -9 during establishment of rat hippocampal synaptic circuitry [J].
Aujla, Paven K. ;
Huntley, George W. .
JOURNAL OF COMPARATIVE NEUROLOGY, 2014, 522 (06) :1249-1263
[14]   Matrix metalloproteases and PAR1 activation [J].
Austin, Karyn M. ;
Covic, Lidija ;
Kuliopulos, Athan .
BLOOD, 2013, 121 (03) :431-439
[15]  
Bach DR, 2017, MOL PSYCHIAT
[16]   Synaptic cell adhesion molecule-2 and collapsin response mediator protein-2 are novel members of the matrix metalloproteinase-9 degradome [J].
Bajor, Malgorzata ;
Michaluk, Piotr ;
Gulyassy, Peter ;
Kekesi, Adrienna Katalin ;
Juhasz, Gabor ;
Kaczmarek, Leszek .
JOURNAL OF NEUROCHEMISTRY, 2012, 122 (04) :775-788
[17]   Ontogeny of MMPs and TIMPs in the Murine Neocortex [J].
Bednarek, Nathalie ;
Clement, Yan ;
Lelievre, Vincent ;
Olivier, Paul ;
Loron, Gauthier ;
Garnotel, Roselyne ;
Gressens, Pierre .
PEDIATRIC RESEARCH, 2009, 65 (03) :296-300
[18]   Caregiver Burden in Bipolar Hypomania and Mania: A Systematic Review [J].
Beentjes, Titus A. A. ;
Goossens, Peter J. J. ;
Poslawsky, Irina E. .
PERSPECTIVES IN PSYCHIATRIC CARE, 2012, 48 (04) :187-197
[19]   Towards a modern classification of the epilepsies? [J].
Berg, Anne T. ;
Cross, J. Helen .
LANCET NEUROLOGY, 2010, 9 (05) :459-461
[20]   Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model [J].
Bilousova, T. V. ;
Dansie, L. ;
Ngo, M. ;
Aye, J. ;
Charles, J. R. ;
Ethell, D. W. ;
Ethell, I. M. .
JOURNAL OF MEDICAL GENETICS, 2009, 46 (02) :94-102