Department of Ophthalmology, Experimental Ophthalmology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Research Department Cell and Gene Therapy, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Cells. 2020 Sep 11;9(9):2082. doi: 10.3390/cells9092082.
We have recently demonstrated that neural stem cell-based intravitreal co-administration of glial cell line-derived neurotrophic factor (GDNF) and ciliary neurotrophic factor (CNTF) confers profound protection to injured retinal ganglion cells (RGCs) in a mouse optic nerve crush model, resulting in the survival of ~38% RGCs two months after the nerve lesion. Here, we analyzed whether this neuroprotective effect is long-lasting and studied the impact of the pronounced RGC rescue on axonal regeneration. To this aim, we co-injected a GDNF- and a CNTF-overexpressing neural stem cell line into the vitreous cavity of adult mice one day after an optic nerve crush and determined the number of surviving RGCs 4, 6 and 8 months after the lesion. Remarkably, we found no significant decrease in the number of surviving RGCs between the successive analysis time points, indicating that the combined administration of GDNF and CNTF conferred lifelong protection to injured RGCs. While the simultaneous administration of GDNF and CNTF stimulated pronounced intraretinal axon growth when compared to retinas treated with either factor alone, numbers of regenerating axons in the distal optic nerve stumps were similar in animals co-treated with both factors and animals treated with CNTF only.
我们最近的研究表明,神经干细胞来源的胶质细胞系源性神经营养因子(GDNF)和睫状神经营养因子(CNTF)的玻璃体内共给药,在小鼠视神经挤压模型中对损伤的视网膜神经节细胞(RGC)有显著的保护作用,导致神经损伤后两个月时约有 38%的 RGC 存活。在这里,我们分析了这种神经保护作用是否具有持久性,并研究了明显的 RGC 挽救对轴突再生的影响。为此,我们在视神经挤压后一天将过表达 GDNF 和 CNTF 的神经干细胞系共注射到成年小鼠的玻璃体腔中,并在损伤后 4、6 和 8 个月时确定存活的 RGC 数量。值得注意的是,我们在连续分析时间点之间没有发现存活的 RGC 数量显著减少,表明 GDNF 和 CNTF 的联合给药对损伤的 RGC 提供了终身保护。虽然与单独用任何一种因子处理的视网膜相比,GDNF 和 CNTF 的同时给药刺激了明显的视网膜内轴突生长,但在同时用两种因子处理的动物和仅用 CNTF 处理的动物的远端视神经残端中的再生轴突数量相似。