ADAMTS expression and function in central nervous system injury and disorders

被引:60
|
作者
Gottschall, Paul E. [1 ]
Howell, Matthew D. [2 ]
机构
[1] Univ Arkansas Med Sci, Dept Pharmacol & Toxicol, Little Rock, AR 72205 USA
[2] Iowa State Univ, Dept Biomed Sci, Ames, IA 50011 USA
关键词
Brevican; Chondroitin sulfate; Spinal cord injury; Seizure; Neuroplasticity; Glial scar; Proteolytic fragment; CHONDROITIN SULFATE PROTEOGLYCANS; EXTRACELLULAR-MATRIX; THROMBOSPONDIN MOTIFS; SPINAL-CORD; PROTEOLYTIC CLEAVAGE; DENTATE-GYRUS; METALLOPROTEINASE; DISINTEGRIN; BREVICAN; BRAIN;
D O I
10.1016/j.matbio.2015.01.014
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
The components of the adult extracellular matrix in the central nervous system form a lattice-like structure that is deposited as perineuronal nets, around axon initial segments and as synapse-associated matrix. An abundant component of this matrix is the lecticans, chondroitin sulfate-bearing proteoglycans that are the major substrate for several members of the ADAMTSs (a disintegrin and metalloproteinase with thrombospondin motifs) family. Since lecticans are key regulators of neural plasticity, ADAMTS cleavage of lecticans would likely also contribute to neuroplasticity. Indeed, many studies have examined the neuroplastic contribution of the ADAMTSs to damage and recovery after injury and in central nervous system disease. Much of this data supports a role for the ADAMTSs in recovery and repair following spinal cord injury by stimulating axonal outgrowth after degradation of a glial scar and improving synaptic plasticity following seizure-induced neural damage in the brain. The action of the ADAMTSs in chronic diseases of the central nervous system appears to be more complex and less well-defined. Increasing evidence indicates that lecticans participate in synaptic plasticity in neurodegenerative disease states. It will be interesting to examine how ADAMTS expression and action would affect the progression of these diseases. (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:70 / 76
页数:7
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