Department of Orthopedics, Xijing Hospital, The Fourth Military Medical University, Xi'an 710032, PR China.
Injury. 2013 Jul;44(7):941-6. doi: 10.1016/j.injury.2013.03.029. Epub 2013 Apr 30.
In the previous study, we attempted to use a collagen-chitosan (CCH) scaffold to mimic the bio-functional peripheral nerve and to bridge sciatic nerve defects in rats. The results demonstrated that it could support and guide the nerve regeneration after three months. In the current study, a type of peptide which carried RGD sequences was connected to the CCH surface by a chemical method. After this process, the microtubule structure of the scaffold was not changed. Then the coated scaffolds were used to repair a 15mm sciatic nerve defect in rats. Four weeks after implantation, linear growth of axons in the longitudinal structure was observed, and the number of regenerated axons remarkably increased. Two months later, the scaffold was partly absorbed and replaced by large quantity of regenerated axons. Importantly, the functional examinations also support the morphological results. Compared with the CCH group, all of the achievements revealed the superior function of RGD-CCH in the rapid regeneration of injured sciatic nerve.
在之前的研究中,我们试图使用胶原-壳聚糖(CCH)支架来模拟生物功能化的周围神经,并桥接大鼠的坐骨神经缺损。结果表明,它可以在三个月后支持和引导神经再生。在本研究中,通过化学方法将一种携带 RGD 序列的肽连接到 CCH 表面。经过这个过程,支架的微管结构没有改变。然后,将涂覆的支架用于修复大鼠 15mm 的坐骨神经缺损。植入后 4 周,观察到沿纵向结构的轴突线性生长,再生轴突的数量显著增加。两个月后,支架部分被吸收并被大量再生轴突取代。重要的是,功能检查也支持形态学结果。与 CCH 组相比,所有这些结果都表明 RGD-CCH 在快速再生受损坐骨神经方面具有优越的功能。