Kim Byung G, Dai Hai-Ning, McAtee Marietta, Bregman Barbara S
Department of Neuroscience, Georgetown University Medical Center, Washington, DC 20007, USA.
J Comp Neurol. 2008 May 20;508(3):473-86. doi: 10.1002/cne.21686.
Incomplete spinal cord injury (SCI) elicits structural plasticity of the spared motor system, including the motor cortex, which may underlie some of the spontaneous recovery of motor function seen after injury. Promoting structural plasticity may become an important component of future strategies to improve functional outcomes. We have recently observed dynamic changes in the density and morphology of dendritic spines in the motor cortex following SCI. The present study sought to test whether SCI-induced changes in spine density and morphology could be modulated by potential strategies to enhance functional recovery. We examined the effects of enriched environment, transplants, and neurotrophin-3 on the plasticity of synaptic structures in the motor cortex following SCI. Housing rats in an enriched environment increased spine density in the motor cortex regardless of injury. SCI led to a more slender and elongated spine morphology. Enriched housing mitigated the SCI-induced morphological alterations, suggesting that the environmental modification facilitates maturation of synaptic structures. Transplantation of embryonic spinal cord tissue and delivery of neurotrophin-3 at the injury site further increased spine density when combined with enriched housing. This combinatorial treatment completely abolished the injury-induced changes, restoring a preinjury pattern of spine morphology. These results demonstrated that remodeling of dendritic spines in the motor cortex after SCI can be modulated by enriched housing, and the combinatorial treatment with embryonic transplants and neurotrophin-3 can potentiate the effects of enriched housing. We suggest that synaptic remodeling processes in the motor cortex can be targeted for an intervention to enhance functional recovery after SCI.
不完全性脊髓损伤(SCI)会引发保留的运动系统(包括运动皮层)的结构可塑性,这可能是损伤后运动功能出现一些自发恢复的基础。促进结构可塑性可能会成为未来改善功能结局策略的一个重要组成部分。我们最近观察到脊髓损伤后运动皮层中树突棘的密度和形态发生了动态变化。本研究旨在测试脊髓损伤诱导的树突棘密度和形态变化是否可以通过增强功能恢复的潜在策略来调节。我们研究了丰富环境、移植和神经营养因子-3对脊髓损伤后运动皮层突触结构可塑性的影响。将大鼠饲养在丰富环境中可增加运动皮层中的树突棘密度,与损伤情况无关。脊髓损伤导致树突棘形态更加细长。丰富的饲养环境减轻了脊髓损伤诱导的形态学改变,表明环境改变促进了突触结构的成熟。当与丰富的饲养环境相结合时,胚胎脊髓组织移植和在损伤部位递送神经营养因子-3进一步增加了树突棘密度。这种联合治疗完全消除了损伤诱导的变化,恢复了损伤前的树突棘形态模式。这些结果表明,脊髓损伤后运动皮层中树突棘的重塑可以通过丰富的饲养环境来调节,并且胚胎移植和神经营养因子-3的联合治疗可以增强丰富饲养环境的效果。我们建议,运动皮层中的突触重塑过程可以作为干预靶点,以增强脊髓损伤后的功能恢复。