Department of Neuroscience and Center for Brain and Spinal Cord Repair, Wexner Medical Center, The Ohio State University, 460 w 12 Ave, Columbus, OH 43210, USA.
Neural Regen Res. 2014 Feb 15;9(4):356-61. doi: 10.4103/1673-5374.128236.
Axon growth is a central event in the development and post-injury plasticity of the nervous system. Growing axons encounter a wide variety of environmental instructions. Much like traffic lights in controlling the migrating axons, chondroitin sulfate proteoglycans (CSPGs) and heparan sulfate proteoglycans (HSPGs) often lead to "stop" and "go" growth responses in the axons, respectively. Recently, the LAR family and NgR family molecules were identified as neuronal receptors for CSPGs and HSPGs. These discoveries provided molecular tools for further study of mechanisms underlying axon growth regulation. More importantly, the identification of these proteoglycan receptors offered potential therapeutic targets for promoting post-injury axon regeneration.
轴突生长是神经系统发育和损伤后可塑性的核心事件。生长中的轴突会遇到各种各样的环境指令。就像交通信号灯控制着迁移中的轴突一样,软骨素硫酸盐蛋白聚糖(CSPGs)和硫酸乙酰肝素蛋白聚糖(HSPGs)通常分别导致轴突的“停止”和“前进”生长反应。最近,LAR 家族和 NgR 家族分子被鉴定为 CSPGs 和 HSPGs 的神经元受体。这些发现为进一步研究轴突生长调控机制提供了分子工具。更重要的是,这些蛋白聚糖受体的鉴定为促进损伤后轴突再生提供了潜在的治疗靶点。