Tissue Engineering Research Group (TERG), Department of Anatomy, Royal College of Surgeons in Ireland, Dublin, Ireland; Advanced Materials and Bioengineering Research (AMBER) Centre, Royal College of Surgeons in Ireland and Trinity College Dublin, Ireland; Trinity Centre for Bioengineering (TCBE), Trinity College Dublin, Ireland.
Department of Physiology and Medical Physics, Centre for the Study of Neurological Disorders, Microsurgical Research and Training Facility, Royal College of Surgeons in Ireland, Dublin, Ireland.
J Control Release. 2019 Jun 28;304:51-64. doi: 10.1016/j.jconrel.2019.05.001. Epub 2019 May 2.
Neurotrophic factor delivery via biodegradable nerve guidance conduits may serve as a promising treatment for the repair of large peripheral nerve defects. However, a platform for controlled delivery is required because of their short in vivo half-life and their potential to impede axonal regeneration when used in supraphysiological doses. In this study, we investigated the dose-dependent, synergistic and temporal effects of NGF and GDNF on neurite outgrowth, adult dorsal root ganglia axonal outgrowth, Schwann cell migration and cytokine production in vitro. Using the optimal dose and combination of NGF and GDNF, we developed a PLGA microparticle-based delivery platform to control their delivery. The dose-dependent effects of both NGF and GDNF individually were found to be non-linear with a saturation point. However, the synergistic effect between NGF and GDNF was found to outweigh their dose-dependent effects in terms of enhancing Schwann cell migration and axonal outgrowth while allowing a 100-fold reduction in dose. Moreover, a temporal profile that mimics the physiological flux of NGF and GDNF in response to injury, compared to one that resembles an early burst release delivery profile, was found to enhance their bioactivity. The optimized NGF- and GDNF-loaded microparticles were then incorporated into a guidance conduit, and their capacity to enhance nerve regeneration across a 15 mm sciatic nerve defect in rats was demonstrated. Enhanced nerve regeneration was seen in comparison to non-treated defects and very encouragingly, to a similar level compared to the clinical gold standard of autograft. Taken together, we suggest that this delivery platform might have significant potential in the field of peripheral nerve repair; allowing spatial and temporal control over the delivery of potent neurotrophic factors to enhance the regenerative capacity of biomaterials-based nerve guidance conduits.
神经营养因子通过可生物降解的神经引导导管输送可能成为修复大的周围神经缺损的一种很有前途的治疗方法。然而,由于其体内半衰期短,并且当以超生理剂量使用时可能会阻碍轴突再生,因此需要一个控制释放的平台。在这项研究中,我们研究了 NGF 和 GDNF 对体外神经突生长、成年背根神经节轴突生长、施万细胞迁移和细胞因子产生的剂量依赖性、协同作用和时间效应。使用 NGF 和 GDNF 的最佳剂量和组合,我们开发了一种基于 PLGA 微球的输送平台来控制它们的输送。发现 NGF 和 GDNF 各自的剂量依赖性效应是非线性的,存在饱和点。然而,NGF 和 GDNF 之间的协同效应在增强施万细胞迁移和轴突生长方面超过了它们的剂量依赖性效应,同时使剂量减少了 100 倍。此外,与类似于早期爆发释放输送谱的时间谱相比,模拟 NGF 和 GDNF 对损伤的生理通量的时间谱被发现可以增强它们的生物活性。然后将优化的负载 NGF 和 GDNF 的微球掺入到引导导管中,并证明它们能够增强大鼠 15mm 坐骨神经缺损处的神经再生。与未经处理的缺陷相比,增强的神经再生,非常令人鼓舞的是,与自体移植物的临床金标准相比,达到了类似的水平。总之,我们认为这种输送平台在外周神经修复领域具有重要的潜力;允许对有潜力的神经营养因子进行时空控制释放,以增强基于生物材料的神经引导导管的再生能力。