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Resorbable structures for schwann cell enhanced peripheral nerve regeneration

机译:Schwann细胞增强周围神经再生的可再吸收结构

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Schwann cells play a dual role serving as a physical framework for regenerating nerves, providing extracellular matrix proteins and specific adhesion molecules facilitating attachment and cell movement, and as a source of stimulatory factors mediated by the release or reception of different ligands important in growth and cell signaling events. To investigate the role of one such ligand, glial growth factor (GGF), in peripheral nerve regeneration, a bioabsorbable nerve guide, prepared from a poly(lactic-co-glycolic) acid (PLGA) foam was seeded with autogenous Schwann cells in the presence and absence of growth factor and evaluated in vivo using a rat sciatic nerve regeneration model. Four weeks post-operatively peripheral nerve regeneration was evident. The resorbable foam implant demonstrated extensive neo-vascularization in and around the guide with no evidence of an inflammatory response or encapsulation. The study showed a statistically significant increase in all measured parameters of nerve regeneration in the presence of GGF. Increased numbers of blood vessels in the regenerated tissue accompanied increased total axon counts after twelve weeks. The addition of exogenous Schwann cells resulted in reduced total axon counts perhaps due to the competition for limited growth factors released by the regenerating tissues. The Schwann cell groups, however, displayed the highest myelination indices recorded likely reflecting the role of Schwann cells in the myelination process. Measurements of conduction velocities (EMGs) revealed the highest conductance velocities recorded in nerves regenerated in the presence of both GGF and Schwann cells. Clearly, the inclusion of GGF in the nerve regenerative process is beneficial with respect to both the generation of new axons and the establishment of a functional endpoint.
机译:Schwann细胞发挥用作再生神经的物理框架的双重作用,提供细胞外基质蛋白质和促进附着和细胞运动的特定粘合分子,并且作为由生长和细胞中重要的不同配体的释放或接收介导的刺激因子来源信令事件。为了探讨一种这样的配体,胶质生长因子(GGF),在外周神经再生中,从聚(乳酸二乙醇酸)酸(PLGA)泡沫制备的生物可吸收神经引导件中的生物可吸收神经引导件生长因子的存在与不存在,并使用大鼠坐骨神经再生模型在体内评估。可操作性外周枢神经再生后四周是明显的。可再吸收的泡沫植入物在导向器上和周围的广泛新血管化,没有炎症反应或封装的证据。该研究表明,GGF存在下神经再生的所有测量参数的统计学显着增加。再生组织中的血管数量增加伴随了12周后的总轴突数。由于再生组织释放的有限生长因子的竞争,添加外源施旺细胞的增加可能减少了总轴突数。然而,施万细胞组展示了可能反映了施万细胞在髓鞘过程中的作用的最高髓鞘指标。传导速度(EMG)的测量显示出在GGF和Schwann细胞的存在下再生的神经中记录的最高导电速度。显然,在神经再生过程中包含GGF对新轴突的产生和创作终点的建立是有益的。

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