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自对准施万细胞单层表现出固有能力来引导轴突生长。

Self-aligned Schwann cell monolayers demonstrate an inherent ability to direct neurite outgrowth.

机构信息

Center for Biotechnology and Interdisciplinary Studies, Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY, USA.

出版信息

J Neural Eng. 2010 Aug;7(4):046001. doi: 10.1088/1741-2560/7/4/046001. Epub 2010 May 20.

DOI:10.1088/1741-2560/7/4/046001
PMID:20489238
Abstract

In vivo nerve guidance channel studies have identified Schwann cell (SC) presence as an integral factor in axonal number and extension in an injury site, and in vitro studies have provided evidence that oriented SCs can direct neurite outgrowth. However, traditional methods used to create oriented SC monolayers (e.g. micropatterns/microtopography) potentially introduce secondary guidance cues to the neurons that are difficult to de-couple. Although SCs expanded on uniform laminin-coated coverslips lack a global orientation, the monolayers contain naturally formed regions of locally oriented cells that can be used to investigate SC-mediated neurite guidance. In this work, novel image analysis techniques have been developed to quantitatively assess local neurite orientation with respect to the underlying regional orientation of the Schwann cell monolayer. Results confirm that, in the absence of any secondary guidance cues, a positive correlation exists between neurite outgrowth and regional orientation of the SC monolayer. Thus, SCs alone possess an inherent ability to direct neurite outgrowth, and expansion of the co-culture-based quantitative method described can be used to further deconstruct specific biomolecular mechanisms of neurite guidance.

摘要

体内神经引导通道研究已经确定施万细胞(Schwann cell,SC)的存在是损伤部位轴突数量和延伸的一个重要因素,体外研究也提供了证据表明定向 SC 可以引导神经突生长。然而,用于创建定向 SC 单层(例如微图案/微形貌)的传统方法可能会向神经元引入难以分离的次要引导线索。尽管在均匀涂覆层粘连蛋白的盖玻片上扩展的 SC 缺乏整体方向,但单层包含自然形成的局部定向细胞区域,可用于研究 SC 介导的神经突引导。在这项工作中,开发了新的图像分析技术来定量评估局部神经突相对于 Schwann 细胞单层的底层区域方向的取向。结果证实,在不存在任何次要引导线索的情况下,神经突生长与 SC 单层的区域方向之间存在正相关。因此,SC 本身具有引导神经突生长的固有能力,并且可以进一步分解神经突引导的特定生物分子机制来扩展基于共培养的定量方法。

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