Department of Biochemistry, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Department of Biochemistry, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Biochim Biophys Acta Gen Subj. 2017 Oct;1861(10):2435-2441. doi: 10.1016/j.bbagen.2017.06.005. Epub 2017 Jun 6.
Therapeutics specific to neural injury have long been anticipated but remain unavailable. Axons in the central nervous system do not readily regenerate after injury, leading to dysfunction of the nervous system. This failure of regeneration is due to both the low intrinsic capacity of axons for regeneration and the various inhibitors emerging upon injury. After many years of concerted efforts, however, these hurdles to axon regeneration have been partially overcome.
This review summarizes the mechanisms regulating axon regeneration. We highlight proteoglycans, particularly because it has become increasingly clear that these proteins serve as critical regulators for axon regeneration.
Studies on proteoglycans have revealed that glycans not only assist in the modulation of protein functions but also act as main players-e.g., as functional ligands mediating intracellular signaling through specific receptors on the cell surface. By regulating clustering of the receptors, glycans in the proteoglycan moiety, i.e., glycosaminoglycans, promote or inhibit axon regeneration. In addition, proteoglycans are involved in various types of neural plasticity, ranging from synaptic plasticity to experience-dependent plasticity.
Although studies on proteins have progressively facilitated our understanding of the nervous system, glycans constitute a new frontier for further research and development in this field. This article is part of a Special Issue entitled Neuro-glycoscience, edited by Kenji Kadomatsu and Hiroshi Kitagawa.
针对神经损伤的治疗方法一直备受期待,但仍未问世。中枢神经系统中的轴突在受伤后不易再生,导致神经系统功能障碍。这种再生失败既归因于轴突自身再生能力低,也归因于损伤后出现的各种抑制剂。然而,经过多年的协同努力,这些轴突再生的障碍已部分得到克服。
本文总结了调节轴突再生的机制。我们重点介绍了蛋白聚糖,特别是因为越来越清楚的是,这些蛋白质是轴突再生的关键调节因子。
蛋白聚糖的研究揭示了聚糖不仅有助于调节蛋白质的功能,而且还作为主要参与者发挥作用,例如作为功能性配体,通过细胞表面上的特定受体介导细胞内信号转导。通过调节受体的聚集,蛋白聚糖部分中的聚糖,即糖胺聚糖,促进或抑制轴突再生。此外,蛋白聚糖还参与各种类型的神经可塑性,从突触可塑性到经验依赖性可塑性。
尽管对蛋白质的研究逐渐促进了我们对神经系统的理解,但聚糖构成了该领域进一步研究和开发的新前沿。本文是由 Kenji Kadomatsu 和 Hiroshi Kitagawa 编辑的特刊“神经糖科学”的一部分。