Wolfson Centre for Age-Related Diseases, King's College London, Guy's Campus, London Bridge, SE1 1UL, UK.
Exp Neurol. 2012 May;235(1):5-17. doi: 10.1016/j.expneurol.2011.08.008. Epub 2011 Aug 16.
Chondroitin sulphate proteoglycans (CSPGs) are a family of inhibitory extracellular matrix molecules that are highly expressed during development, where they are involved in processes of pathfinding and guidance. CSPGs are present at lower levels in the mature CNS, but are highly concentrated in perineuronal nets where they play an important role in maintaining stability and restricting plasticity. Whilst important for maintaining stable connections, this can have an adverse effect following insult to the CNS, restricting the capacity for repair, where enhanced synapse formation leading to new connections could be functionally beneficial. CSPGs are also highly expressed at CNS injury sites, where they can restrict anatomical plasticity by inhibiting sprouting and reorganisation, curbing the extent to which spared systems may compensate for the loss function of injured pathways. Modification of CSPGs, usually involving enzymatic degradation of glycosaminoglycan chains from the CSPG molecule, has received much attention as a potential strategy for promoting repair following spinal cord and brain injury. Pre-clinical studies in animal models have demonstrated a number of reparative effects of CSPG modification, which are often associated with functional recovery. Here we discuss the potential of CSPG modification to stimulate restorative plasticity after injury, reviewing evidence from studies in the brain, the spinal cord and the periphery.
硫酸软骨素蛋白聚糖(CSPGs)是一类抑制性细胞外基质分子家族,在发育过程中高度表达,参与了轨迹形成和导向的过程。CSPGs 在成熟的中枢神经系统中的表达水平较低,但在神经周细胞网络中高度集中,在那里它们对维持稳定性和限制可塑性起着重要作用。虽然对于维持稳定的连接很重要,但这在中枢神经系统受到损伤后会产生不利影响,限制了修复的能力,因为增强的突触形成导致新的连接可能在功能上是有益的。CSPGs 在外周神经系统损伤部位也高度表达,它们可以通过抑制发芽和重组来限制解剖可塑性,抑制受损通路丧失功能时,受保护系统代偿的程度。CSPGs 的修饰(通常涉及对 CSPG 分子中的糖胺聚糖链进行酶降解)作为促进脊髓和脑损伤后修复的潜在策略受到了广泛关注。动物模型的临床前研究已经证明了 CSPG 修饰的许多修复作用,这些作用通常与功能恢复有关。在这里,我们讨论了 CSPG 修饰刺激损伤后恢复性可塑性的潜力,回顾了来自大脑、脊髓和外周的研究证据。