Department of Biomedical Engineering and Center for Biotechnology and Interdisciplinary Studies, Renssalaer Polytechnic Institute , Troy, New York.
Tissue Eng Part A. 2014 Feb;20(3-4):494-506. doi: 10.1089/ten.TEA.2013.0012. Epub 2013 Dec 11.
Endogenous electric fields are instructive during embryogenesis by acting to direct cell migration, and postnatally, they can promote axonal growth after injury (McCaig 1991, Al-Majed 2000). However, the mechanisms for these changes are not well understood. Application of an appropriate electrical stimulus may increase the rate and success of nerve repair by directly promoting axonal growth. Previously, DC electrical stimulation at 50 mV/mm (1 mA, 8 h duration) was shown to promote neurite outgrowth and a more pronounced effect was observed if both peripheral glia (Schwann cells) and neurons were co-stimulated. If electrical stimulation is delivered to an injury site, both the neurons and all resident non-neuronal cells [e.g., Schwann cells, endothelial cells, fibroblasts] will be treated and this biophysical stimuli can influence axonal growth directly or indirectly via changes to the resident, non-neuronal cells. In this work, non-neuronal cells were electrically stimulated, and changes in morphology and neuro-supportive cells were evaluated. Schwann cell response (morphology and orientation) was examined after an 8 h stimulation over a range of DC fields (0-200 mV/mm, DC 1 mA), and changes in orientation were observed. Electrically prestimulating Schwann cells (50 mV/mm) promoted 30% more neurite outgrowth relative to co-stimulating both Schwann cells with neurons, suggesting that electrical stimulation modifies Schwann cell phenotype. Conditioned medium from the electrically prestimulated Schwann cells promoted a 20% increase in total neurite outgrowth and was sustained for 72 h poststimulation. An 11-fold increase in nerve growth factor but not brain-derived neurotrophic factor or glial-derived growth factor was found in the electrically prestimulated Schwann cell-conditioned medium. No significant changes in fibroblast or endothelial morphology and neuro-supportive behavior were observed poststimulation. Electrical stimulation is widely used in clinical settings; however, the rational application of this cue may directly impact and enhance neuro-supportive behavior, improving nerve repair.
内源性电场在胚胎发生过程中通过指导细胞迁移起指导作用,并且在出生后,它们可以促进损伤后的轴突生长(McCaig 1991,Al-Majed 2000)。然而,这些变化的机制尚不清楚。应用适当的电刺激可以通过直接促进轴突生长来提高神经修复的速度和成功率。以前,已经显示 50 mV/mm(1 mA,8 小时持续时间)的直流电刺激可促进神经突生长,如果同时刺激周围神经胶质(施万细胞)和神经元,则观察到更明显的效果。如果将电刺激施加到损伤部位,神经元和所有驻留的非神经元细胞[例如,施万细胞,内皮细胞,成纤维细胞]都将被处理,这种生物物理刺激可以直接或间接地通过改变驻留的非神经元细胞来影响轴突生长。在这项工作中,对非神经元细胞进行了电刺激,并评估了形态和神经营养细胞的变化。在 0-200 mV/mm(直流 1 mA)的范围内对 Schwann 细胞进行 8 小时刺激后,研究了 Schwann 细胞的反应(形态和取向),并观察到取向的变化。相对于同时刺激 Schwann 细胞和神经元,对 Schwann 细胞进行电预刺激(50 mV/mm)可使神经突生长增加 30%,这表明电刺激改变了 Schwann 细胞表型。电预刺激 Schwann 细胞的条件培养基可促进总神经突生长增加 20%,并且在刺激后 72 小时内持续增加。在电预刺激 Schwann 细胞的条件培养基中发现神经生长因子增加了 11 倍,但脑源性神经营养因子或胶质衍生的生长因子没有增加。刺激后,未观察到成纤维细胞或内皮细胞形态和神经营养行为的明显变化。电刺激在临床环境中广泛使用;然而,这种线索的合理应用可能会直接影响和增强神经营养行为,从而改善神经修复。