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Neuroscience
その場で有髄軸索のスペクトル反射型顕微鏡
その場で有髄軸索のスペクトル反射型顕微鏡
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
Spectral Reflectometric Microscopy on Myelinated Axons In Situ

その場で有髄軸索のスペクトル反射型顕微鏡

Full Text
7,786 Views
09:13 min
July 2, 2018

DOI: 10.3791/57965-v

Junhwan Kwon1,2, Myunghwan Choi1,2

1Department of Biomedical Engineering,Sungkyunkwan University, 2Center for Neuroscience Imaging Research,Institute for Basic Science (IBS)

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This study presents a technique for imaging myelinated axons in fixed brain slices utilizing a label-free nanoscale imaging approach based on spectral reflectometry. The method enables analysis of myelin plasticity and demyelination without the need for complex sample preparation.

Key Study Components

Area of Science

  • Neuroscience
  • Axon Imaging
  • Myelin Research

Background

  • Traditional imaging techniques often require complex labeling.
  • Understanding myelin plasticity is crucial for insights into neurodegenerative diseases.
  • The technique can be extended for use in living animals.
  • Label-free approaches minimize disturbances to tissue structure.

Purpose of Study

  • To provide a protocol for studying myelinated axons in fixed tissue.
  • To offer a method for investigating questions surrounding myelin and axonal health.
  • To demonstrate the application of nanoscale imaging in neuroscience research.

Methods Used

  • The primary platform used is spectral reflectometry for imaging.
  • The biological model includes fixed mouse brain slices.
  • No multiomics or metabolic analyses are mentioned in the study.
  • Key steps include tissue fixing and slicing before imaging.
  • Nail polish is used to seal coverslips for preventing contamination.

Main Results

  • SpeRe imaging accurately localized signals along myelinated axons.
  • The method produced results in alignment with traditional fluorescence techniques.
  • No saturation was observed in spectral imaging, validating the reliability of the technique.
  • The imaging allowed for measurement of axon diameter correlating well with fluorescence-based results.

Conclusions

  • This study enables effective imaging of myelinated axons without complex preparations.
  • The technique aids in understanding myelination mechanisms and their plasticity.
  • It presents potential for adaptations in studying living tissues and other neurological questions.

Frequently Asked Questions

What are the advantages of this imaging technique?
The label-free nanoscale imaging technique allows researchers to study myelinated axons without the complications of dye-based labeling.
How is the biological model implemented?
The biological model involves fixing and slicing mouse brain tissue, which is then prepared for imaging using the spectral reflectometry technique.
What types of data are obtained from the imaging?
Data includes the localization of reflectant spectra along myelinated axons and measurements of axon diameter.
How can this method be adapted for living animals?
The protocols can be extended from fixed tissue to living models, enhancing its utility in dynamic studies of myelination.
What are the key limitations of this technique?
Background noise can occur due to the use of silica coverslips, which may affect imaging quality if not properly managed.
What critical steps are involved in the imaging process?
Key steps include glass slide preparation, tissue placement, and careful sealing to prevent contamination before imaging.
Can this technique be used for other types of neural studies?
While specifically aimed at studying myelin, adaptations for other neural structures may be possible, pending validation.

イメージング分光反射率に基づくラベル無料ナノを使用して固定脳スライスの髄軸索をイメージングのためのステップバイ ステップ プロトコルを紹介します。

この技術は、ミエリンの可塑性や脱髄など、ミエリン分野の重要な質問に答えるのに役立ちます。この技術の主な利点は、複雑な標識やサンプル調製なしで、無傷の脳組織における有髄軸索のナノ構造を研究できることです。ここでは、脳のスライスでのアプリケーションを示しますが、この手法は生きている動物に拡張できます。

テキストプロトコルに従ってマウス脳組織を固定しスライスした後、各組織スライスごとにスライドガラス1個とカバーグラス2個を準備します。ガラスカッターを使用して、正方形のカバーグラスの1つを半分に切ります。次に、瞬間接着剤を使用してスペーサーを作成し、2つのピースをスライドガラスに取り付けます。

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