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Comprehensive strategy of conduit guidance combined with VEGF producing Schwann cells accelerates peripheral nerve repair

机译:导管综合指导策略与VEGF生产施万细胞加速外周神经修复

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摘要

Peripheral nerve regeneration requires stepwise and well-organized establishment of microenvironment. Since local delivery of VEGF-A in peripheral nerve repair is expected to promote angiogenesis in the microenvironment and Schwann cells (SCs) play critical role in nerve repair, combination of VEGF and Schwann cells may lead to efficient peripheral nerve regeneration. VEGF-A overexpressing Schwann cells were established and loaded into the inner wall of hydroxyethyl cellulose/soy protein isolate/polyaniline sponge (HSPS) conduits. When HSPS is mechanically distorted, it still has high durability of strain strength, thus, can accommodate unexpected strain of nerve tissues in motion. A 10 mm nerve defect rat model was used to test the repair performance of the HSPS-SC (VEGF) conduits, meanwhile the HSPS, HSPS-SC, HSPS-VEGF conduits and autografts were worked as controls. The immunofluorescent co-staining of GFP/VEGF-A, Ki67 and MBP showed that the VEGF-A overexpressing Schwann cells could promote the proliferation, migration and differentiation of Schwann cells as the VEGF-A was secreted from the VEGF-A overexpressing Schwann cells. The nerve repair performance of the multifunctional and flexible conduits was examined though rat behavioristics, electrophysiology, nerve innervation to gastrocnemius muscle (GM), toluidine blue (TB) staining, transmission electron microscopy (TEM) and NF200/S100 double staining in the regenerated nerve. The results displayed that the effects on the repair of peripheral nerves in HSPS-SC (VEGF) group was the best among the conduits groups and closed to autografts. HSPS-SC (VEGF) group exhibited notably increased CD31+ endothelial cells and activation of VEGFR2/ERK signaling pathway in the regenerated nerve tissues, which probably contributed to the improved nerve regeneration. Altogether, the comprehensive strategy including VEGF overexpressing Schwann cells-mediated and HSPS conduit-guided peripheral nerve repair provides a new avenue for nerve tissue engineering.
机译:周围神经再生需要逐步且有组织的微环境建立。由于预期在外周神经修复中的VEGF-A局部递送,预计在微环境和施旺细胞(SCS)中促进血管生成,因此在神经修复中发挥关键作用,VEGF和SCHWANN细胞的组合可能导致有效的周围神经再生。 VEGF-A过表达Schwann细胞建立并装入羟乙基纤维素/大豆蛋白分离物/聚苯胺海绵(HSP)管道的内壁中。当HSP机械扭曲时,它仍然具有高耐久性的应变强度,因此可以适应运动中的意外的神经组织菌株。使用10mm神经缺损大鼠模型来测试HSPS-SC(VEGF)管道的修复性能,同时HSP,HSPS-SC,HSPS-VEGF导管和自体移植物作为对照。 GFP / VEGF-A,KI67和MBP的免疫荧光共染色表明,VEGF-A过表达施旺细胞可以促进Schwann细胞的增殖,迁移和分化,因为VEGF-A从VEGF-A过表达的Schwann细胞分泌。研究了多功能和柔性导管的神经修复性能,尽管大鼠行为学,电生理学,神经检查到胃肠肌(GM),甲苯胺蓝(TB)染色,透射电子显微镜(TEM)和NF200 / S100在再生神经中的双重染色。结果显示,对HSPS-SC(VEGF)组外周神经修复的影响是导管组中的最佳状态,并关闭自体移植物。 HSPS-SC(VEGF)组显着增加了CD31 +内皮细胞,并在再生神经组织中激活VEGFR2 / ERK信号通路,这可能导致改善的神经再生。总共,包括VEGF过表达的施万细胞介导的综合策略和HSPS管道引导的周围神经修复为神经组织工程提供了新的途径。

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