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诱导周围神经再生中Büngner带形成的策略。

Strategies for inducing the formation of bands of Büngner in peripheral nerve regeneration.

作者信息

Ribeiro-Resende Victor T, Koenig Brigitte, Nichterwitz Susanne, Oberhoffner Sven, Schlosshauer Burkhard

机构信息

NMI Naturwissenschaftliches und Medizinisches, Institut an der Universität Tübingen, Markwiesenstr. 55, D-72770 Reutlingen, Germany.

出版信息

Biomaterials. 2009 Oct;30(29):5251-9. doi: 10.1016/j.biomaterials.2009.07.007. Epub 2009 Jul 26.

Abstract

Peripheral human nerves fail to regenerate across longer tube implants (>2 cm), most likely because implants lack the microarchitecture of native nerves, including bands of Büngner. Bands of Büngner comprise longitudinally aligned Schwann cell strands that guide selectively regrowing axons. We aim to optimize tubular implants by integrating artificial bands of Büngner. Three principle strategies for inducing the formation of bands of Büngner were investigated: (a) an aligned extracellular matrix, (b) polarizing differentiation factors, and (c) microstructured biomaterial filaments. In vitro oriented collagen and a combination of differentiation factors (NGF, neuregulin-1, TGF-beta) induced Schwann cell alignment to some extent. The most pronounced Schwann cell alignment was evident on ultrathin, endless poly-epsilon-caprolactone (PCL) filaments with longitudinal microgrooves. Precoated PCL filaments proved to be non-cytotoxic, displayed good cell attachment, and supported Schwann cell proliferation as well as guided axonal outgrowth. In vitro on PCL filaments Schwann cells displayed a polarized expression of the cell adhesion molecule L1 similar to that seen in vivo in bands of Büngner after sciatic nerve crush in adult rats. In summary, the integration of bioengineered bands of Büngner based on microstructured polymer filaments in nerve conduits promises to be the most valuable approach to initiating a more efficient regeneration across longer nerve lesions.

摘要

人体外周神经无法在较长的管状植入物(>2厘米)中再生,最可能的原因是植入物缺乏天然神经的微观结构,包括许旺氏带。许旺氏带由纵向排列的施万细胞链组成,可引导选择性再生的轴突。我们旨在通过整合人工许旺氏带来优化管状植入物。研究了诱导形成许旺氏带的三种主要策略:(a)排列的细胞外基质,(b)极化分化因子,以及(c)微结构化生物材料细丝。体外定向胶原和分化因子(NGF、神经调节蛋白-1、TGF-β)的组合在一定程度上诱导了施万细胞的排列。在具有纵向微槽的超薄、无端聚己内酯(PCL)细丝上,施万细胞排列最为明显。预涂覆的PCL细丝被证明无细胞毒性,具有良好的细胞附着性,并支持施万细胞增殖以及引导轴突生长。在体外,PCL细丝上的施万细胞表现出细胞粘附分子L1的极化表达,类似于成年大鼠坐骨神经挤压后体内许旺氏带中的情况。总之,在神经导管中整合基于微结构化聚合物细丝的生物工程化许旺氏带有望成为一种最有价值的方法,以启动更长神经损伤的更有效再生。

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