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Neuroscience
視床皮質軸索分岐とシナプスの可視化脊髄共培養系における形成
視床皮質軸索分岐とシナプスの可視化脊髄共培養系における形成
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
Visualization of Thalamocortical Axon Branching and Synapse Formation in Organotypic Cocultures

視床皮質軸索分岐とシナプスの可視化脊髄共培養系における形成

Full Text
6,938 Views
06:16 min
March 28, 2018

DOI: 10.3791/56553-v

Naoyuki Matsumoto1,2, Nobuhiko Yamamoto2

1Department of Medical Neuroscience, Graduate School of Medical Sciences,Kanazawa University, 2Neuroscience Laboratories, Graduate School of Frontier Biosciences,Osaka University

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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 protocol for simultaneous imaging of thalamocortical axon branching and synapse formation in organotypic cocultures of the thalamus and cerebral cortex. It focuses on dynamic morphological changes in the thalamocortical projection, providing insights into new neural circuit formation and the relationship between axon growth and synapse development.

Key Study Components

Area of Science

  • Neuroscience
  • Neurobiology
  • Cell Biology

Background

  • Thalamocortical projections play a critical role in sensory processing.
  • Understanding axon branching and synapse formation is essential for insights into neural circuit formation.
  • Current methods have limitations in observing these changes simultaneously at the cellular level.
  • The study advances techniques for imaging in living cell contexts.

Purpose of Study

  • To investigate dynamic morphological changes during axon branching and synapse formation.
  • To provide a method that allows observation of individual living cells in coculture.
  • To assess the relationship between axon growth and synaptic development in thalamocortical neurons.

Methods Used

  • Organotypic cocultures of thalamic and cortical slices were utilized.
  • Rat postnatal day two tissue was used to create the biological model.
  • Electroporation was performed to introduce fluorescent markers for imaging.
  • Cultures were maintained at 37 degrees Celsius and observed over specific developmental time points.
  • Imaging was conducted using a confocal microscope to capture axonal dynamics.

Main Results

  • Dynamic changes in axon branching and synapse formation were observed, highlighting plasticity in thalamocortical projections.
  • Discrete accumulation of synaptic markers along axons was noted, indicating ongoing synaptic development.
  • The technique allowed for real-time observation of morphological changes in individual cells.
  • Findings emphasize the potential for investigating gene roles in axon and synapse dynamics.

Conclusions

  • This study demonstrates a novel method for exploring neural circuit dynamics and plasticity.
  • It provides insights into the coupling of axon growth and synapse formation.
  • The findings have implications for understanding mechanisms of neural connectivity and plasticity in health and disease.

Frequently Asked Questions

What are the advantages of this imaging protocol?
This protocol allows simultaneous imaging of axon branching and synapse formation, providing a dynamic view of neural development.
How are the cortical and thalamic tissues prepared for the study?
Tissue is obtained from postnatal day two rats, carefully dissected, and cultured in serum-containing medium to maintain viability.
What types of data can be obtained using this method?
Researchers can obtain imaging data showing axonal growth patterns and synaptic development, along with insights into the underlying biological processes.
How can this method be applied to other neural circuits?
The technique can be adapted to study intrinsic connections in the cerebral cortex or other neural networks by altering the biological models utilized.
Are there any limitations to this imaging technique?
While effective, the method relies on the viability of cultured slices, which can vary due to handling or environmental conditions.

このプロトコルでは、視床皮質軸索分岐およびシナプス形成の脊髄共培養系における視床と大脳皮質の同時イメージング法について説明します。個々 の視床皮質軸索とその神経終末は、下流と GFP タグ シナプトフィジン単細胞エレクトロポレーション法による可視化します。

この方法の全体的な目標は、視床皮質投影における軸索分岐とシナプス形成の動的な形態学的変化を研究することです。この方法は、新しい神経回路形成など、神経生物学の分野における重要な質問に答えるのに役立ちます。この手法の主な利点は、個々の生細胞における軸索の成長とシナプス形成の同時観察です。

この方法は、視床皮質突起における軸索分岐とシナプス形成との関係についての洞察を提供することができます。また、大脳皮質の内因性接続など、他の神経回路にも適用できます。この手順を開始するには、すべての手術器具を70%エタノールで10分以上滅菌します。

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