Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.
Biotechnol Bioeng. 2013 Mar;110(3):947-57. doi: 10.1002/bit.24750. Epub 2012 Nov 1.
After injury to the central nervous system, a glial scar develops that physically and biochemically inhibits axon growth. In the scar, activated astrocytes secrete inhibitory extracellular matrix, of which chondroitin sulfate proteoglycans (CSPGs) are considered the major inhibitory component. An inhibitory interface of CSPGs forms around the lesion and prevents axons from traversing the injury, and decreasing CSPGs can enhance axon growth. In this report, we established an in vitro interface model of activated astrocytes and subsequently investigated gene delivery as a means to reduce CSPG levels and enhance axon growth. In the model, a continuous interface of CSPG producing astrocytes was created with neurons seeded opposite the astrocytes, and neurite crossing, stopping, and turning were evaluated as they approached the interface. We investigated the efficacy of lentiviral delivery to degrade or prevent the synthesis of CSPGs, thereby removing CSPG inhibition of neurite growth. Lentiviral delivery of RNAi targeting two key CSPG synthesis enzymes, chondroitin polymerizing factor and chondroitin synthase-1, decreased CSPGs, and reduced inhibition by the interface. Degradation of CSPGs by lentiviral delivery of chondroitinase also resulted in less inhibition and more neurites crossing the interface. These results indicate that the interface model provides a tool to investigate interventions that reduce inhibition by CSPGs, and that gene delivery can be effective in promoting neurite growth across an interface of CSPG producing astrocytes.
中枢神经系统损伤后,会形成神经胶质瘢痕,其在物理和生化上抑制轴突生长。在瘢痕中,活化的星形胶质细胞分泌抑制性细胞外基质,其中硫酸软骨素蛋白聚糖 (CSPGs) 被认为是主要的抑制性成分。CSPGs 在病变周围形成抑制性界面,阻止轴突穿过损伤部位,减少 CSPGs 可以促进轴突生长。在本报告中,我们建立了活化星形胶质细胞的体外界面模型,随后研究了基因传递作为降低 CSPG 水平和促进轴突生长的一种手段。在该模型中,在神经元种子对面培养星形胶质细胞,形成 CSPG 产生星形胶质细胞的连续界面,并评估神经元突起接近界面时的穿越、停止和转向。我们研究了慢病毒传递降解或防止 CSPG 合成的效果,从而消除 CSPG 对神经突生长的抑制作用。针对两个关键 CSPG 合成酶(软骨素聚合因子和软骨素合成酶-1)的 RNAi 的慢病毒传递降低了 CSPGs,并减少了界面的抑制作用。慢病毒传递软骨素酶降解 CSPGs 也导致更少的抑制和更多的神经突穿过界面。这些结果表明,该界面模型提供了一种工具来研究减少 CSPG 抑制的干预措施,并且基因传递可以有效地促进 CSPG 产生星形胶质细胞界面处的神经突生长。