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Fetal extracellular matrix nerve wraps locally improve peripheral nerve remodeling after complete transection and direct repair in rat

机译:胎儿细胞外基质神经包裹在局部横断并直接修复大鼠后局部改善周围神经重塑

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摘要

In peripheral nerve (PN) injuries requiring surgical repair, as in PN transection, cellular and ECM remodeling at PN epineurial repair sites is hypothesized to reduce PN functional outcomes by slowing, misdirecting, or preventing axons from regrowing appropriately across the repair site. Herein this study reports on deriving and analyzing fetal porcine urinary bladder extracellular matrix (fUB-ECM) by vacuum assisted decellularization, fabricating fUBM-ECM nerve wraps, and testing fUB-ECM nerve wrap biocompatibility and bioactivity in a trigeminal, infraorbital nerve (ION) branch transection and direct end-to-end repair model in rat. FUB-ECM nerve wraps significantly improved epi- and endoneurial organization and increased both neovascularization and growth associated protein-43 (GAP-43) expression at PN repair sites, 28-days post surgery. However, the number of neurofilament positive axons, remyelination, and whisker-evoked response properties of ION axons were unaltered, indicating improved tissue remodeling per se does not predict axon regrowth, remyelination, and the return of mechanoreceptor cortical signaling. This study shows fUB-ECM nerve wraps are biocompatible, bioactive, and good experimental and potentially clinical devices for treating epineurial repairs. Moreover, this study highlights the value provided by precise, analytic models, like the ION repair model, in understanding how PN tissue remodeling relates to axonal regrowth, remyelination, and axonal response properties.
机译:在需要进行外科手术修复的周围神经(PN)损伤中,如在PN横断中,假设在PN肾上腺修复位点的细胞和ECM重塑可通过减慢,错误引导或防止轴突在整个修复位点上适当生长而降低PN功能结局。本文的研究报道了通过真空辅助脱细胞,制备fUBM-ECM神经膜和测试fUB-ECM神经膜在三叉神经,眶下神经中的生物相容性和生物活性,来衍生和分析胎儿猪膀胱膀胱细胞外基质(fUB-ECM)。大鼠分支横切和直接端对端修复模型。 FUB-ECM神经包裹物可显着改善上皮和神经内膜组织,并在术后28天在PN修复位点增加新血管形成和生长相关蛋白43(GAP-43)的表达。然而,ION轴突的神经丝阳性轴突,髓鞘再生和晶须诱发的反应特性的数量没有改变,这表明改善的组织重塑本身并不能预测轴突再生,髓鞘再生和机械感受器皮质信号传导的恢复。这项研究表明,fUB-ECM神经膜具有生物相容性,生物活性,并且是治疗海马神经修复的良好实验和潜在临床装置。此外,本研究强调了精确的分析模型(如ION修复模型)在了解PN组织重塑与轴突再生,髓鞘再生和轴突反应特性之间的关系时所提供的价值。

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