Department of Plastic, Reconstructive Surgery, University Hospital of Lausanne (CHUV), Rue du Bugnon 46, 1011 Lausanne, Switzerland.
Section for Anatomy, Department of Integrative Medical Biology, Umeå universitet, hus H, Biologihuset, SE-901 87 Umeå, Sweden.
Neurosci Lett. 2014 Jun 20;572:26-31. doi: 10.1016/j.neulet.2014.04.029. Epub 2014 May 2.
Collagen nerve guides are used clinically for peripheral nerve defects, but their use is generally limited to lesions up to 3 cm. In this study we combined collagen conduits with cells as an alternative strategy to support nerve regeneration over longer gaps. In vitro cell adherence to collagen conduits (NeuraGen(®) nerve guides) was assessed by scanning electron microscopy. For in vivo experiments, conduits were seeded with either Schwann cells (SC), SC-like differentiated bone marrow-derived mesenchymal stem cells (dMSC), SC-like differentiated adipose-derived stem cells (dASC) or left empty (control group), conduits were used to bridge a 1cm gap in the rat sciatic nerve and after 2-weeks immunohistochemical analysis was performed to assess axonal regeneration and SC infiltration. The regenerative cells showed good adherence to the collagen walls. Primary SC showed significant improvement in distal stump sprouting. No significant differences in proximal regeneration distances were noticed among experimental groups. dMSC and dASC-loaded conduits showed a diffuse sprouting pattern, while SC-loaded showed an enhanced cone pattern and a typical sprouting along the conduits walls, suggesting an increased affinity for the collagen type I fibrillar structure. NeuraGen(®) guides showed high affinity of regenerative cells and could be used as efficient vehicle for cell delivery. However, surface modifications (e.g. with extracellular matrix molecule peptides) of NeuraGen(®) guides could be used in future tissue-engineering applications to better exploit the cell potential.
胶原神经导管临床上用于周围神经缺损,但一般仅限于 3cm 以内的病变。本研究将胶原导管与细胞联合应用作为支持更长间隙神经再生的替代策略。通过扫描电子显微镜评估细胞在胶原导管(NeuraGen®神经导管)上的黏附。在体内实验中,将 Schwann 细胞(SCs)、分化为SCs 样的骨髓间充质干细胞(dMSCs)、分化为SCs 样的脂肪间充质干细胞(dASCs)或空白导管(对照组)接种于导管中,用于桥接大鼠坐骨神经 1cm 间隙,2 周后进行免疫组织化学分析,评估轴突再生和SCs 浸润情况。再生细胞与胶原壁有良好的黏附。原代SCs 在远端神经残端的发芽有显著改善。实验组之间近端再生距离无明显差异。负载 dMSC 和 dASC 的导管表现出弥漫性发芽模式,而负载SCs 的导管表现出增强的圆锥状发芽模式和沿导管壁的典型发芽模式,提示对 I 型胶原纤维结构的亲和力增加。NeuraGen®导管对再生细胞具有高亲和力,可作为细胞输送的有效载体。然而,NeuraGen®导管的表面修饰(例如,细胞外基质分子肽)可用于未来的组织工程应用,以更好地利用细胞潜力。