Shakhbazau Antos, Archibald Simon J, Shcharbin Dzmitry, Bryszewska Maria, Midha Rajiv
Department of Clinical Neuroscience, Faculty of Medicine, University of Calgary, HMRB 109-3330 Hospital Drive NW, Calgary, AB, T2N4N1, Canada,
J Mater Sci Mater Med. 2014 Aug;25(8):1979-89. doi: 10.1007/s10856-014-5224-2. Epub 2014 May 7.
The development of artificial off-the-shelf conduits that facilitate effective nerve regeneration and recovery after repair of traumatic nerve injury gaps is of fundamental importance. Collagen-glycosaminoglycan (GAG) matrix mimicking Schwann cell (SC) basal lamina has been proposed as a suitable and biologically rational substrate for nerve regeneration. In the present study, we have focused on the permissiveness of this matrix type for SC migration and repopulation, as these events play an essential role in nerve remodeling. We have also demonstrated that SCs cultured within collagen-GAG matrix are compatible with non-viral dendrimer-based gene delivery, that may allow conditioning of matrix-embedded cells for future gene therapy applications.
开发能够促进创伤性神经损伤间隙修复后有效神经再生和恢复的人工现成导管至关重要。模仿施万细胞(SC)基膜的胶原蛋白-糖胺聚糖(GAG)基质已被提议作为神经再生的合适且具有生物学合理性的底物。在本研究中,我们重点关注了这种基质类型对SC迁移和再填充的允许性,因为这些事件在神经重塑中起着至关重要的作用。我们还证明,在胶原蛋白-GAG基质中培养的SCs与基于非病毒树枝状大分子的基因递送兼容,这可能允许对基质包埋细胞进行预处理以用于未来的基因治疗应用。