Clements Isaac P, Kim Young-tae, English Arthur W, Lu Xi, Chung Andy, Bellamkonda Ravi V
Neurological Biomaterials and Cancer Therapeutics, Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology/Emory University, Suite 3108, 313 Ferst Dr., Atlanta, GA 30332-0535, USA.
Biomaterials. 2009 Aug;30(23-24):3834-46. doi: 10.1016/j.biomaterials.2009.04.022. Epub 2009 May 15.
It has been demonstrated that nerve guidance channels containing stacked thin-films of aligned poly(acrylonitrile-co-methylacrylate) fibers support peripheral nerve regeneration across critical sized nerve gaps, without the aid of exogenous cells or proteins. Here, we explore the ability of tubular channels minimally supplemented with aligned nanofiber-based thin-films to promote endogenous nerve repair. We describe a technique for fabricating guidance channels in which individual thin-films are fixed into place within the lumen of a polysulfone tube. Because each thin-film is <10 microm thick, this technique allows fine control over the positioning of aligned scaffolding substrate. We evaluated nerve regeneration through a 1-film guidance channel--containing a single continuous thin-film of aligned fibers--in comparison to a 3-film channel that provided two additional thin-film tracks. Thirty rats were implanted with one of the two channel types, and regeneration across a 14 mm tibial nerve gap was evaluated after 6 weeks and 13 weeks, using a range of morphological and functional measures. Both the 1-film and the 3-film channels supported regeneration across the nerve gap resulting in functional muscular reinnervation. Each channel type characteristically influenced the morphology of the regeneration cable. Interestingly, the 1-film channels supported enhanced regeneration compared to the 3-film channels in terms of regenerated axon profile counts and measures of nerve conduction velocity. These results suggest that minimal levels of appropriately positioned topographical cues significantly enhance guidance channel function by modulating endogenous repair mechanisms, resulting in effective bridging of critically sized peripheral nerve gaps.
已证明,包含排列的聚丙烯腈 - 甲基丙烯酸甲酯纤维堆叠薄膜的神经导向通道能够在无外源性细胞或蛋白质帮助的情况下,支持周围神经跨越临界尺寸的神经间隙再生。在此,我们探究了用排列的纳米纤维基薄膜进行最小程度补充的管状通道促进内源性神经修复的能力。我们描述了一种制造导向通道的技术,其中单个薄膜固定在聚砜管腔内的适当位置。由于每个薄膜厚度小于10微米,该技术允许对排列的支架底物的定位进行精细控制。我们通过包含单个连续排列纤维薄膜的单膜导向通道评估神经再生,并与提供另外两条薄膜轨迹的三膜通道进行比较。30只大鼠植入两种通道类型中的一种,在6周和13周后,使用一系列形态学和功能测量方法评估跨越14毫米胫神经间隙的再生情况。单膜通道和三膜通道均支持神经间隙的再生,从而实现功能性肌肉再支配。每种通道类型都对再生束的形态有独特影响。有趣的是,在再生轴突轮廓计数和神经传导速度测量方面,单膜通道比三膜通道支持更强的再生。这些结果表明,适当定位的地形线索的最低水平通过调节内源性修复机制显著增强导向通道功能,从而有效桥接临界尺寸的周围神经间隙。