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作为人工轴突的镀膜玻璃和聚丙交酯乙交酯微纤维。

Coated glass and vicryl microfibers as artificial axons.

作者信息

Howe Charles L

机构信息

Department of Neuroscience and Neurology, Mayo Clinic College of Medicine, Rochester, Minn, USA.

出版信息

Cells Tissues Organs. 2006;183(4):180-94. doi: 10.1159/000096509.

Abstract

The complex interactions that occur between oligodendrocytes and axons during the process of central nervous system myelination and remyelination remain unclear. Elucidation of the cell-biological and -biochemical mechanisms supporting myelin production and elaboration requires a robust in vitro system that recapitulates the relationship between axons and oligodendrocytes in a manner that is open to molecular dissection. We provide evidence for an artificial axon culture system in which we observed oligodendrocytes extending large plasma membrane projections that frequently completely ensheathed fibers coated with a variety of extracellular matrix molecules. These membrane projections varied in extent and thickness depending upon the substrate and upon the diameter of the coated fiber. Matrigel-coated glass microfibers were found to support the development of thick membrane sheaths that extended for hundreds of microns and exhibited many features suggestive of the potential for true myelin deposition. Likewise, Matrigel-coated Vicryl fibers supported plasma membrane extensions that covered extremely large surface areas and occasionally wrapped the coated Vicryl fibers in more than one membrane layer. Our findings suggest that the deposition of molecular cues onto glass or polymer fibers either via adsorption or chemical modification may be a useful tool for the discovery or validation of axonal factors critical for myelination and remyelination. Herein, we provide evidence that polyglactin 910 and glass microfibers coated with adhesion factors may provide a reasonable system for the in vitro analysis of myelination, and may eventually serve a role in engineering artificial systems for neural repair.

摘要

在中枢神经系统髓鞘形成和再髓鞘形成过程中,少突胶质细胞与轴突之间发生的复杂相互作用仍不清楚。要阐明支持髓鞘产生和形成的细胞生物学及生物化学机制,需要一个强大的体外系统,该系统能以一种便于分子剖析的方式重现轴突与少突胶质细胞之间的关系。我们提供了一种人工轴突培养系统的证据,在该系统中,我们观察到少突胶质细胞伸出大的质膜突起,这些突起常常完全包裹着涂有多种细胞外基质分子的纤维。这些膜突起的范围和厚度因底物以及被包裹纤维的直径而异。发现基质胶包被的玻璃微纤维能支持厚膜鞘的形成,厚膜鞘可延伸数百微米,并展现出许多表明有真正髓鞘沉积潜力的特征。同样,基质胶包被的聚丙交酯乙交酯纤维能支持质膜延伸,这些延伸覆盖极大的表面积,偶尔会用不止一层膜包裹被包被的聚丙交酯乙交酯纤维。我们的研究结果表明,通过吸附或化学修饰将分子信号沉积到玻璃或聚合物纤维上,可能是发现或验证对髓鞘形成和再髓鞘形成至关重要的轴突因子的有用工具。在此,我们提供证据表明,聚乳酸 - 乙醇酸共聚物910和涂有黏附因子的玻璃微纤维可能为髓鞘形成的体外分析提供一个合理的系统,并最终可能在构建用于神经修复的人工系统中发挥作用。

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