首页> 外文期刊>Neural regeneration research >Decellularized optic nerve functional scaffold transplant facilitates directional axon regeneration and remyelination in the injured white matter of the rat spinal cord
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Decellularized optic nerve functional scaffold transplant facilitates directional axon regeneration and remyelination in the injured white matter of the rat spinal cord

机译:脱细胞的视神经功能支架移植促进了大鼠脊髓受伤的白质的定向轴突再生和重新髓鞘

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Axon regeneration and remyelination of the damaged region is the most common repair strategy for spinal cord injury. However, achieving good outcome remains difficult. Our previous study showed that porcine decellularized optic nerve better mimics the extracellular matrix of the embryonic porcine optic nerve and promotes the directional growth of dorsal root ganglion neurites. However, it has not been reported whether this material promotes axonal regeneration in vivo. In the present study, a porcine decellularized optic nerve was seeded with neurotrophin-3-overexpressing Schwann cells. This functional scaffold promoted the directional growth and remyelination of regenerating axons. In vitro, the porcine decellularized optic nerve contained many straight, longitudinal channels with a uniform distribution, and microscopic pores were present in the channel wall. The spatial micro topological structure and extracellular matrix were conducive to the adhesion, survival and migration of neural stem cells. The scaffold promoted the directional growth of dorsal root ganglion neurites, and showed strong potential for myelin regeneration. Furthermore, we transplanted the porcine decellularized optic nerve containing neurotrophin-3-overexpressing Schwann cells in a rat model of T10 spinal cord defect in vivo. Four weeks later, the regenerating axons grew straight, the myelin sheath in the injured/transplanted area recovered its structure, and simultaneously, the number of inflammatory cells and the expression of chondroitin sulfate proteoglycans were reduced. Together, these findings suggest that porcine decellularized optic nerve loaded with Schwann cells overexpressing neurotrophin-3 promotes the directional growth of regenerating spinal cord axons as well as myelin regeneration. All procedures involving animals were conducted in accordance with the ethical standards of the Institutional Animal Care and Use Committee of Sun Yat-sen University (approval No. SYSU-IACUC-2019-B034) on February 28, 2019.
机译:受损区域的轴突再生和重新髓质是脊髓损伤最常见的修复策略。然而,实现了良好的结果仍然很困难。我们以前的研究表明,猪脱细胞的视神经更好地模仿胚胎猪视神经的细胞外基质,促进背根神经节神经纳的定向生长。但是,尚未报告这种材料是否促进体内轴突再生。在本研究中,用神经营养蛋白-3过表达施曼细胞接种猪脱细胞的视神经。这种功能性支架促进了再生轴突的定向生长和重新髓。体外,猪脱细胞的视神经含有许多具有均匀分布的直线,纵向通道,并且在通道壁中存在微观孔隙。空间微拓扑结构和细胞外基质有利于神经干细胞的粘附,存活和迁移。支架促进背根神经节神经菌素的定向生长,并表现出髓鞘再生的强大潜力。此外,我们在体内T10脊髓缺损的大鼠模型中移植含有神经营养蛋白-3过度抑制的氏氏氏氏氏氏氏氏血管细胞。四周后,再生轴突在损伤/移植区域中的髓鞘恢复,同时,减少了炎症细胞的数量和软骨素硫酸软骨素蛋白多糖的表达。这些研究结果表明,随着过表达神经滋生蛋白-3的施旺细胞负载的猪脱细胞视神经促进再生脊髓轴突以及髓鞘再生的定向生长。涉及动物的所有程序是根据孙中山大学的制度畜牧业和使用委员会的道德标准(批准号Sysu-Iacuc-2019-B034)进行的。

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