Xu X M, Guénard V, Kleitman N, Aebischer P, Bunge M B
Chambers Family Electron Microscopy Laboratory, Miami Project to Cure Paralysis, University of Miami School of Medicine, Florida 33136, USA.
Exp Neurol. 1995 Aug;134(2):261-72. doi: 10.1006/exnr.1995.1056.
We previously demonstrated that Schwann cells (SCs) in semipermeable guidance channels promote axonal regeneration in adult rat spinal cord transected at the mid-thoracic level. Propriospinal but not supraspinal axons grew into these channels. Here, we tested the ability of exogenous brain-derived neurotrophic factor (BDNF) and neurotrophin-3 (NT-3) to promote axonal regeneration in this novel model. The two neurotrophins were delivered simultaneously into the channel by an Alzet minipump at a rate of 12 micrograms/day for each neurotrophin for 14 of 30 days tested; phosphate-buffered saline, the vehicle solution, was used as a control. Significantly more myelinated nerve fibers were present in SC/neurotrophin grafts than in SC/vehicle grafts (1523 +/- 292 vs 882 +/- 287). In the graft, at least 5 mm from the rostral cord-graft interface, some nerve fibers were immunoreactive for serotonin, a neurotransmitter specific to raphe-derived axons in rat spinal cord. Fast blue retrograde tracing from SC/neurotrophin grafts revealed labeled neurons in 10 nuclei of the brain stem, 67% of these being in the lateral and spinal vestibular nuclei. The mean number of labeled brain stem neurons in the SC/neurotrophin group (92; n = 3) contrasted with the mean in the SC/vehicle group (6; n = 4). Our results clearly demonstrate that BDNF and NT-3 infusion enhanced propriospinal axonal regeneration and, more significantly, promoted axonal regeneration of specific distant populations of brain stem neurons into grafts at the mid-thoracic level in adult rat spinal cord.
我们之前证明,半透性引导通道中的施万细胞(SCs)可促进成年大鼠胸段中段横断脊髓的轴突再生。脊髓固有轴突而非脊髓上轴突长入这些通道。在此,我们在这个新模型中测试了外源性脑源性神经营养因子(BDNF)和神经营养素-3(NT-3)促进轴突再生的能力。在测试的30天中的14天,通过Alzet微型泵以每种神经营养因子每天12微克的速率将这两种神经营养因子同时输送到通道中;使用磷酸盐缓冲盐水(载体溶液)作为对照。与SC/载体移植组相比,SC/神经营养因子移植组中存在明显更多的有髓神经纤维(1523±292对882±287)。在移植体中,距头端脊髓-移植体界面至少5毫米处,一些神经纤维对5-羟色胺呈免疫反应,5-羟色胺是大鼠脊髓中缝衍生轴突特有的神经递质。从SC/神经营养因子移植体进行的快蓝逆行追踪显示,在脑干的10个核中有标记的神经元,其中67%位于外侧和脊髓前庭核。SC/神经营养因子组中标记的脑干神经元的平均数(92;n = 3)与SC/载体组中的平均数(6;n = 4)形成对比。我们的结果清楚地表明,BDNF和NT-3输注增强了脊髓固有轴突再生,更显著的是,促进了成年大鼠脊髓胸段中段特定远距离脑干神经元群体的轴突再生进入移植体。