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Neuroscience
マウス脳スライスにおける長距離入力の光遺伝学的刺激のための生体内脳内立体注射
マウス脳スライスにおける長距離入力の光遺伝学的刺激のための生体内脳内立体注射
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
In Vivo Intracerebral Stereotaxic Injections for Optogenetic Stimulation of Long-Range Inputs in Mouse Brain Slices

マウス脳スライスにおける長距離入力の光遺伝学的刺激のための生体内脳内立体注射

Full Text
12,333 Views
09:07 min
September 20, 2019

DOI: 10.3791/59534-v

Louis Richevaux1,2, Louise Schenberg1,2, Mathieu Beraneck1,2, Desdemona Fricker1,2

1CNRS (Integrative Neuroscience and Cognition Center, UMR 8002), 2Université Paris Descartes, Sorbonne Paris Cité

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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 protocol outlines methods for identifying the cell-type specific functional connectivity of long-range inputs from distant brain regions using optogenetic stimulation in ex vivo brain slices. The study employs photostimulation to activate specific axon terminals, enabling researchers to investigate synaptic responses in targeted neuronal populations.

Key Study Components

Area of Science

  • Neuroscience
  • Electrophysiology
  • Optogenetics

Background

  • Understanding functional connectivity in the brain is crucial for elucidating neuronal networks.
  • Optogenetics allows for precise control of neuronal activity using light.
  • The method utilizes ex vivo brain slices to facilitate cellular recordings and manipulations.

Purpose of Study

  • To explore the functional connections between specific brain regions.
  • To assess the excitatory and inhibitory responses of targeted neurons following stimulation.
  • To establish a protocol that can be broadly applied to different neuronal types and connections.

Methods Used

  • Utilizes ex vivo brain slices from anesthetized animals.
  • Specific brain regions are targeted for optogenetic manipulation using light-sensitive ion channels.
  • Critical steps include surgical preparation, viral injection, and slice preparation.
  • Whole-cell patch-clamp recording is performed to measure neuronal responses.

Main Results

  • Demonstrated that light stimulation elicits excitatory post-synaptic potentials in pyramidal neurons.
  • Responses varied with light intensity, indicating modulation of synaptic efficacy.
  • Identified synaptic transmission dynamics in presubicular neurons via current clamp measurements.

Conclusions

  • This study provides a robust protocol for investigating long-range functional connectivity in the brain.
  • Highlights the potential of optogenetic techniques to elucidate synaptic mechanisms and connectivity patterns.
  • Contributes to the understanding of how different neuronal populations interact and process information.

Frequently Asked Questions

What are the advantages of using ex vivo brain slices?
Ex vivo brain slices allow for direct electrophysiological recordings while preserving the overall network architecture of the brain, enabling detailed studies of synaptic interactions.
How are specific brain regions targeted in this protocol?
Targeting is achieved through stereotaxic surgery, which allows for precise positioning of injections and stimulation sites in the desired brain area.
What types of data can be obtained from patch-clamp recordings?
Patch-clamp recordings provide insights into the excitability of neurons, synaptic responses, and the dynamics of neurotransmitter release in response to stimulation.
How can the method be adapted for different neuronal types?
By using different viral constructs coding for various light-sensitive channels, researchers can target a wide range of neuronal populations and study their unique connectivity patterns.
What limitations should be considered when using this method?
Limitations include the potential alteration of synaptic properties due to the slice preparation and the inability to observe metabotropic signaling pathways effectively.

このプロトコルは、ex vivo脳スライスにおける光遺伝学的刺激を用いて、遠方の脳領域からの長距離入力の細胞型特異的機能的接続性を同定する一連の方法を説明する。

この方法の目的は、脳スライスにおける光刺激を用いて、遠くの脳領域からの長距離入力の機能的な結合性を同定することである。光感受性イオンチャネルの様々な媒介発現のための特定の脳領域の立体的標的化は、光でその領域から来る軸索の選択的刺激を可能にする。この手順をデモンストレーションすることは、私のグループの博士課程の学生、ルイ・リシュヴォーです。

手術前に、動物がつま先ピンチで十分に麻酔されていることを確認してください。呼吸を容易にするために舌をそっと引き出す。次に、頭蓋毛を剃ります。

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