Cerri Federica, Salvatore Luca, Memon Danish, Boneschi Filippo Martinelli, Madaghiele Marta, Brambilla Paola, Del Carro Ubaldo, Taveggia Carla, Riva Nilo, Trimarco Amelia, Lopez Ignazio D, Comi Giancarlo, Pluchino Stefano, Martino Gianvito, Sannino Alessandro, Quattrini Angelo
Division of Neuroscience and INSPE, San Raffaele Scientific Institute, via Olgettina 60, 20132 Milan, Italy.
Department of Innovation Engineering, University of Lecce, Via per Monteroni, 73100 Lecce, Italy.
Biomaterials. 2014 Apr;35(13):4035-4045. doi: 10.1016/j.biomaterials.2014.01.069. Epub 2014 Feb 20.
Several bioengineering approaches have been proposed for peripheral nervous system repair, with limited results and still open questions about the underlying molecular mechanisms. We assessed the biological processes that occur after the implantation of collagen scaffold with a peculiar porous micro-structure of the wall in a rat sciatic nerve transection model compared to commercial collagen conduits and nerve crush injury using functional, histological and genome wide analyses. We demonstrated that within 60 days, our conduit had been completely substituted by a normal nerve. Gene expression analysis documented a precise sequential regulation of known genes involved in angiogenesis, Schwann cells/axons interactions and myelination, together with a selective modulation of key biological pathways for nerve morphogenesis induced by porous matrices. These data suggest that the scaffold's micro-structure profoundly influences cell behaviors and creates an instructive micro-environment to enhance nerve morphogenesis that can be exploited to improve recovery and understand the molecular differences between repair and regeneration.
已经提出了几种用于周围神经系统修复的生物工程方法,但其结果有限,并且关于潜在分子机制的问题仍然存在。与商用胶原蛋白导管和神经挤压损伤相比,我们在大鼠坐骨神经横断模型中,使用功能、组织学和全基因组分析,评估了植入具有特殊壁多孔微结构的胶原蛋白支架后发生的生物学过程。我们证明,在60天内,我们的导管已被正常神经完全替代。基因表达分析记录了参与血管生成、雪旺细胞/轴突相互作用和髓鞘形成的已知基因的精确顺序调节,以及多孔基质诱导的神经形态发生关键生物学途径的选择性调节。这些数据表明,支架的微结构深刻影响细胞行为,并创造了一个指导性的微环境来增强神经形态发生,这可用于改善恢复并理解修复和再生之间的分子差异。