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通过原子力显微镜和共聚焦显微镜同时联用对完整和神经性神经纤维进行纳米级生物物理和结构研究。

Nano-scale Biophysical and Structural Investigations on Intact and Neuropathic Nerve Fibers by Simultaneous Combination of Atomic Force and Confocal Microscopy.

作者信息

Rosso Gonzalo, Liashkovich Ivan, Young Peter, Shahin Victor

机构信息

Institute of Physiology II, WWU MünsterMünster, Germany.

Department of Sleep Medicine and Neuromuscular DisordersMünster, Germany.

出版信息

Front Mol Neurosci. 2017 Aug 30;10:277. doi: 10.3389/fnmol.2017.00277. eCollection 2017.

Abstract

The links between neuropathies of the peripheral nervous system (PNS), including Charcot-Marie-Tooth1A and hereditary neuropathy with liability to pressure palsies, and impaired biomechanical and structural integrity of PNS nerves remain poorly understood despite the medical urgency. Here, we present a protocol describing simultaneous structural and biomechanical integrity investigations on isolated nerve fibers, the building blocks of nerves. Nerve fibers are prepared from nerves harvested from wild-type and exemplary PNS neuropathy mouse models. The basic principle of the designed experimental approach is based on the simultaneous combination of atomic force microscopy (AFM) and confocal microscopy. AFM is used to visualize the surface structure of nerve fibers at nano-scale resolution. The simultaneous combination of AFM and confocal microscopy is used to perform biomechanical, structural, and functional integrity measurements at nano- to micro-scale. Isolation of sciatic nerves and subsequent teasing of nerve fibers take ~45 min. Teased fibers can be maintained at 37°C in a culture medium and kept viable for up to 6 h allowing considerable time for all measurements which require 3-4 h. The approach is designed to be widely applicable for nerve fibers from mice of any PNS neuropathy. It can be extended to human nerve biopsies.

摘要

尽管医学上迫切需要了解,但包括夏科-马里-图思病1A型和遗传性压迫易感性神经病在内的周围神经系统(PNS)神经病变与PNS神经生物力学和结构完整性受损之间的联系仍知之甚少。在此,我们提出了一种方案,描述了对神经的基本组成部分——分离的神经纤维进行结构和生物力学完整性同步研究。神经纤维取自野生型和典型PNS神经病变小鼠模型的神经。所设计的实验方法的基本原理基于原子力显微镜(AFM)和共聚焦显微镜的同步结合。AFM用于在纳米级分辨率下可视化神经纤维的表面结构。AFM和共聚焦显微镜的同步结合用于在纳米到微米尺度上进行生物力学、结构和功能完整性测量。分离坐骨神经并随后梳理神经纤维大约需要45分钟。梳理后的纤维可以在37°C的培养基中保存,并在长达6小时内保持活力,这为所有需要3 - 4小时的测量留出了相当长的时间。该方法设计用于广泛应用于任何PNS神经病变小鼠的神经纤维。它可以扩展到人类神经活检。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6703/5582161/8b652231ed30/fnmol-10-00277-g0001.jpg

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