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三维纳米纤维混合支架引导并增强脊髓损伤后的轴突再生。

Three-Dimensional Nanofiber Hybrid Scaffold Directs and Enhances Axonal Regeneration after Spinal Cord Injury.

作者信息

Milbreta Ulla, Nguyen Lan Huong, Diao Huajia, Lin Junquan, Wu Wutian, Sun Chun-Yang, Wang Jun, Chew Sing Yian

机构信息

School of Chemical and Biomedical Engineering, Nanyang Technological University, 637459, Singapore.

Department of Anatomy, The University of Hong Kong, Li Ka Shing Faculty of Medicine, Pokfulam, Hong Kong SAR, China.

出版信息

ACS Biomater Sci Eng. 2016 Aug 8;2(8):1319-1329. doi: 10.1021/acsbiomaterials.6b00248. Epub 2016 Jul 19.

Abstract

Spinal cord injuries (SCIs) are followed by a complex series of events that contribute to the failure of regeneration. To date, there is no robust treatment that can restore the injury-induced loss of function. Since damaged spinal axons do not spontaneously regenerate in their native inhibitory microenvironment, a combined application of biomaterials and neurotrophic factors that induce nerve regeneration emerges as an attractive treatment for SCIs. In this study, we report the novel use of a three-dimensional (3D) hybrid scaffold to provide contact guidance for regrowth of axons . The scaffold comprises 3D aligned sparsely distributed poly(ε-caprolactone--ethyl ethylene phosphate) nanofibers that are supported and dispersed within a collagen hydrogel. Neurotrophin-3 was incorporated into the scaffold as an additional biochemical signal. To evaluate the efficacy of the scaffold in supporting nerve regeneration after SCIs, the construct was implanted into an incision injury, which was created at level C5 in the rat spinal cord. After 3 months of implantation, scaffolds with NT-3 incorporation showed the highest average neurite length (391.9 ± 12.9 μm, ≤ 0.001) as compared to all the other experimental groups. In addition, these regenerated axons formed along the direction of the aligned nanofibers, regardless of their orientation. Moreover, the presence of the hybrid scaffolds did not affect tissue scarring and inflammatory reaction. Taken together, these findings demonstrate that our scaffold design can serve as a potential platform to support axonal regeneration following SCIs.

摘要

脊髓损伤(SCIs)后会发生一系列复杂事件,这些事件导致再生失败。迄今为止,尚无有效的治疗方法能够恢复损伤所致的功能丧失。由于受损的脊髓轴突在其天然抑制性微环境中不会自发再生,因此联合应用生物材料和诱导神经再生的神经营养因子成为一种有吸引力的脊髓损伤治疗方法。在本研究中,我们报告了一种新型三维(3D)混合支架的应用,该支架可为轴突再生提供接触导向。该支架由三维排列的稀疏分布的聚(ε-己内酯-磷酸乙酯乙烯酯)纳米纤维组成,这些纳米纤维支撑并分散在胶原水凝胶中。神经营养因子-3作为额外的生化信号被掺入支架中。为了评估该支架在脊髓损伤后支持神经再生的效果,将构建体植入大鼠脊髓C5水平处的切口损伤处。植入3个月后,与所有其他实验组相比,掺入NT-3的支架显示出最高的平均神经突长度(391.9±12.9μm,≤0.001)。此外,这些再生轴突沿着排列的纳米纤维方向形成,无论其取向如何。而且,混合支架的存在不影响组织瘢痕形成和炎症反应。综上所述,这些发现表明我们的支架设计可作为脊髓损伤后支持轴突再生的潜在平台。

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