Department of Tissue Engineering, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran 1417743373, Iran.
Research Center for Noncommunicable Diseases, Jahrom University of Medical Sciences, Jahrom 7414846199, Iran.
ACS Biomater Sci Eng. 2023 Jun 12;9(6):3496-3511. doi: 10.1021/acsbiomaterials.3c00157. Epub 2023 May 9.
Nerve guide conduits (NGCs) have been shown to be less efficient than nerve autografts in peripheral nerve regeneration. To address this issue, we developed for the first time a novel tissue-engineered nerve guide conduit structure encapsulated with human endometrial stem cell (EnSC) derived exosomes, which promoted nerve regeneration in rat sciatic nerve defects. In this study, we initially indicated the long-term efficacy and safety impacts of newly designed double layered SF/PLLA nerve guide conduits. Then the regeneration effects of SF/PLLA nerve guide conduits containing exosomes derived from human EnSCs were evaluated in rat sciatic nerve defects. The human EnSC derived exosomes were isolated from the supernatant of human EnSC cultures and characterized. Subsequently, the human EnSC derived exosomes were encapsulated in constructed NGCs by fibrin gel. For in vivo studies, entire 10 mm peripheral nerve defects were generated in rat sciatic nerves and restored with NGC encapsulated with human EnSC derived exosomes (Exo-NGC group), nerve guide conduits, and autografts. The efficiency of the NGCs encapsulated with human EnSCs derived exosomes in assisting peripheral nerve regeneration was investigated and compared with other groups. The in vivo results demonstrated that encapsulated human EnSC derived exosomes in NGC (Exo-NGC) significantly benefitted nerve regeneration based on motor function, sensory reaction, and electrophysiological results. Furthermore, immunohistochemistry with histopathology results showed the formation of regenerated nerve fibers, along with blood vessels that newly were developed, as a result of the exosome functions in the Exo-NGC group. These outcomes illustrated that the newly designed core-shell SF/PLLA nerve guide conduit encapsulated with human EnSC derived exosomes enhanced the regeneration process of axons and improved the functional recovery of rat sciatic nerve defects. So, encapsulated human EnSC-derived exosomes in a core-shell SF/PLLA nerve guide conduit are a potential therapeutic cell-free treatment for peripheral nerve defects.
神经引导导管(NGCs)在周围神经再生中的效率低于神经自体移植物。为了解决这个问题,我们首次开发了一种新型的组织工程神经引导导管结构,该结构被人子宫内膜干细胞(EnSC)衍生的外泌体包裹,促进了大鼠坐骨神经缺损中的神经再生。在这项研究中,我们首先表明了新设计的双层 SF/PLLA 神经引导导管的长期疗效和安全性影响。然后,评估了含有人 EnSC 衍生外泌体的 SF/PLLA 神经引导导管在大鼠坐骨神经缺损中的再生效果。人 EnSC 衍生的外泌体是从人 EnSC 培养物的上清液中分离出来的,并进行了表征。随后,通过纤维蛋白凝胶将人 EnSC 衍生的外泌体包裹在构建的 NGC 中。在体内研究中,在大鼠坐骨神经中产生了整个 10mm 的周围神经缺损,并通过 NGC 包裹人 EnSC 衍生的外泌体(Exo-NGC 组)、神经引导导管和自体移植物进行了修复。研究了包裹有人 EnSC 衍生的外泌体的 NGC 在辅助周围神经再生中的效率,并与其他组进行了比较。体内结果表明,包裹有人 EnSC 衍生的外泌体的 NGC(Exo-NGC)显著促进了神经再生,这是基于运动功能、感觉反应和电生理学结果。此外,免疫组织化学和组织病理学结果表明,由于外泌体在 Exo-NGC 组中的作用,形成了再生的神经纤维和新形成的血管。这些结果表明,新设计的 SF/PLLA 神经引导导管包裹有人 EnSC 衍生的外泌体增强了轴突的再生过程,并改善了大鼠坐骨神经缺损的功能恢复。因此,包裹有人 EnSC 衍生的外泌体的 SF/PLLA 神经引导导管是治疗周围神经缺损的一种有潜力的无细胞治疗方法。