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Neuroscience
Görselleştirme Thalamocortical Axon dallanma ve sinaps oluşumunda Organotypic Cocultures
Görselleştirme Thalamocortical Axon dallanma ve sinaps oluşumunda Organotypic Cocultures
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
Visualization of Thalamocortical Axon Branching and Synapse Formation in Organotypic Cocultures

Görselleştirme Thalamocortical Axon dallanma ve sinaps oluşumunda Organotypic Cocultures

Full Text
6,983 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.

Bu iletişim kuralı thalamocortical akson dallanma ve synapse oluşumu organotypic cocultures, talamus ve serebral korteks eşzamanlı görüntüleme için bir yöntemi açıklar. Bireysel thalamocortical akson ve presynaptic onların terminalleri bir tek hücre çoğalmasıyla tekniği ile DsRed ve synaptophysin GFP öğesini tarafından görüntülenmiştir.

Bu yöntemin genel amacı, talamokortikal projeksiyonda akson dallanmasının ve sinaps oluşumunun dinamik morfolojik değişikliklerini incelemektir. Bu yöntem, yeni nöral devre oluşumu gibi nörobiyoloji alanındaki temel soruların yanıtlanmasına yardımcı olabilir. Bu tekniğin temel avantajı, bireysel canlı hücrelerde akson büyümesinin ve sinaps oluşumunun aynı anda gözlemlenmesidir.

Bu yöntem, talamokortikal projeksiyonlarda akson dallanması ve sinaps oluşumu arasındaki ilişki hakkında fikir verebilir. Serebral korteksteki içsel bağlantı gibi diğer nöral devrelere de uygulanabilir. Bu işleme başlamak için tüm cerrahi aletleri %70 etanol ile 10 dakika veya daha uzun süre sterilize edin.

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