Adams Robert D, Rendell Sara R, Counts Lauren R, Papke Jason B, Willits Rebecca K, Harkins Amy B
Department of Pharmacological and Physiological Science, Saint Louis University, 1402 S. Grand Blvd, St. Louis, MO, 63104, USA.
Ann Biomed Eng. 2014 Jun;42(6):1282-91. doi: 10.1007/s10439-014-1001-0. Epub 2014 Apr 8.
Electrical and chemical stimulation have been studied as potent mechanisms of enhancing nerve regeneration and wound healing. However, it remains unclear how electrical stimuli affect nerve growth, particularly in the presence of neurotrophic factors. The objective of this study was to explore (1) the effect of brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) supplementation to support neurite outgrowth in a 3D scaffold, and (2) the effect of brief, low voltage, electrical stimulation (ES) on neurite outgrowth prior to neurotrophin supplementation. Dissociated E11 chick dorsal root ganglia (DRG) were seeded within a 1.5 mg/mL type-I collagen scaffold. For neurotrophin treatments, scaffolds were incubated for 24 h in culture media containing NGF (10 ng/mL) or BDNF (200 ng/mL), or both. For ES groups, scaffolds containing neurons were stimulated for 10 min at 8-10 V/m DC, then incubated for 24 h with neurotrophin. Fixed and labeled neurons were imaged to measure neurite growth and directionality. BDNF supplementation was not as effective as NGF at supporting DRG neurite outgrowth. ES prior to NGF supplementation improved DRG neurite outgrowth compared to NGF alone. This combination of brief ES with NGF treatment was the most effective treatment compared to NGF or BDNF alone. Brief ES had no impact on neurite directionality in the 3D scaffolds. These results demonstrate that ES improves neurite outgrowth in the presence of neurotrophins, and could provide a potential therapeutic approach to improve nerve regeneration when coupled with neurotrophin treatment.
电刺激和化学刺激已被作为增强神经再生和伤口愈合的有效机制进行研究。然而,电刺激如何影响神经生长仍不清楚,尤其是在存在神经营养因子的情况下。本研究的目的是探讨:(1)补充脑源性神经营养因子(BDNF)和神经生长因子(NGF)对支持三维支架中神经突生长的影响;(2)在补充神经营养因子之前,短暂、低电压电刺激(ES)对神经突生长的影响。将解离的E11鸡背根神经节(DRG)接种于1.5mg/mL的I型胶原支架内。对于神经营养因子处理,将支架在含有NGF(10ng/mL)或BDNF(200ng/mL)或两者的培养基中孵育24小时。对于电刺激组,将含有神经元的支架在8 - 10V/m直流电下刺激10分钟,然后与神经营养因子一起孵育24小时。对固定并标记的神经元进行成像,以测量神经突生长和方向性。补充BDNF在支持DRG神经突生长方面不如补充NGF有效。与单独使用NGF相比,在补充NGF之前进行电刺激可改善DRG神经突生长。与单独使用NGF或BDNF相比,这种短暂电刺激与NGF治疗的组合是最有效的治疗方法。短暂电刺激对三维支架中的神经突方向性没有影响。这些结果表明,电刺激在存在神经营养因子的情况下可改善神经突生长,并且在与神经营养因子治疗相结合时,可为改善神经再生提供一种潜在的治疗方法。