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首页> 外文期刊>Nature methods >A culture system to study oligodendrocyte myelination processes using engineered nanofibers
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A culture system to study oligodendrocyte myelination processes using engineered nanofibers

机译:使用工程化纳米纤维研究少突胶质细胞髓鞘形成过程的培养系统

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摘要

Current methods for studying central nervous system myelination necessitate permissive axonal substrates conducive to myelin wrapping by oligodendrocytes. We have developed a neuron-free culture system in which electron-spun nanofibers of varying sizes substitute for axons as a substrate for oligodendrocyte myelination, thereby allowing manipulation of the biophysical elements of axonal-oligodendroglial interactions. To investigate axonal regulation of myelination, this system effectively uncouples the role of molecular (inductive) cues from that of biophysical properties of the axon. We use this method to uncover the causation and sufficiency of fiber diameter in the initiation of concentric wrapping by rat oligodendrocytes. We also show that oligodendrocyte precursor cells display sensitivity to the biophysical properties of fiber diameter and initiate membrane ensheathment before differentiation. The use of nanofiber scaffolds will enable screening for potential therapeutic agents that promote oligodendrocyte differentiation and myelination and will also provide valuable insight into the processes involved in remyelination.
机译:目前研究中枢神经系统髓鞘形成的方法需要允许的轴突基质,其有助于少突胶质细胞包裹髓鞘。我们已经开发了一种无神经元的培养系统,其中大小不同的电子纺丝纳米纤维替代了轴突,作为少突胶质细胞髓鞘化的底物,从而允许操纵轴突-少突胶质相互作用的生物物理元素。为了研究髓鞘的轴突调节,该系统有效地将分子提示的作用与轴突的生物物理特性分开。我们使用这种方法来揭示大鼠少突胶质细胞同心包缠的起始中纤维直径的原因和充分性。我们还显示少突胶质细胞前体细胞显示出对纤维直径的生物物理特性的敏感性,并在分化前启动了膜的包皮。纳米纤维支架的使用将能够筛选出促进少突胶质细胞分化和髓鞘形成的潜在治疗剂,还将提供有关髓鞘形成过程的宝贵见解。

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