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Neuroscience
Im lebenden Organismus Calcium-Bildgebung neuronaler Ensembles in Netzwerken primärer se...
Im lebenden Organismus Calcium-Bildgebung neuronaler Ensembles in Netzwerken primärer se...
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
In Vivo Calcium Imaging of Neuronal Ensembles in Networks of Primary Sensory Neurons in Intact Dorsal Root Ganglia

Im lebenden Organismus Calcium-Bildgebung neuronaler Ensembles in Netzwerken primärer sensorischer Neurone in intakten dorsalen Wurzelganglien

Full Text
3,698 Views
09:07 min
February 10, 2023

DOI: 10.3791/64826-v

John Shannonhouse1, Ruben Gomez1, Hyeonwi Son1, Yan Zhang1, Yu Shin Kim1,2

1Department of Oral & Maxillofacial Surgery, School of Dentistry,University of Texas Health Science Center at San Antonio, 2Programs in Integrated Biomedical Sciences, Translational Sciences, Biomedical Engineering, Radiological Sciences,University of Texas Health Science Center at San Antonio

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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 describes a surgical technique to expose the dorsal root ganglion (DRG) for GCaMP3 (genetically-encoded calcium indicator) imaging in Pirt-GCaMP3 mice. The study investigates neural responses in primary sensory neurons to various stimuli applied to the ipsilateral hind paw, providing insights into calcium transients associated with pain and allodynia.

Key Study Components

Area of Science

  • Neuroscience
  • Neuroimaging
  • Pain Physiology

Background

  • Dorsal root ganglia house primary sensory neurons involved in pain sensation.
  • GCaMP3 imaging allows real-time monitoring of calcium dynamics in neurons.
  • This approach can elucidate mechanisms underlying pain hypersensitivity.
  • Older methodologies are less suited for expansive neural network analysis.

Purpose of Study

  • To demonstrate a comprehensive method for visualizing calcium transients in sensory neurons.
  • To assess neuronal ensemble responses to nociceptive stimuli.
  • To adapt methodologies for applications in trigeminal or other ganglia studies.

Methods Used

  • Surgical exposure of the lumbar L5 DRG was performed on Pirt-GCaMP3 mice.
  • Calcium imaging was conducted using upright confocal microscopy.
  • A variety of stimuli were applied to the hind paw, including mechanical and thermal stimuli.
  • Specific imaging protocols were utilized to capture spontaneous and stimulus-evoked calcium activity.

Main Results

  • The imaging technique enabled real-time observation of up to 1,800 primary sensory neurons simultaneously.
  • Calcium responses increased significantly during strong stimuli or heat exposure.
  • Observations included calcium transients in the absence of external stimuli, suggesting a baseline level of activity.
  • A systematic process for creating high-quality imaging was established, enhancing data reliability.

Conclusions

  • This protocol provides a robust framework for studying the dynamics of sensory neurons in response to pain stimuli.
  • The findings enhance our understanding of neuronal mechanisms related to pain hypersensitivity.
  • Potential applications include evaluating therapeutic interventions for conditions such as allodynia.

Frequently Asked Questions

What are the advantages of using GCaMP3 for calcium imaging?
GCaMP3 allows for real-time visualization of calcium dynamics in living neurons, providing insights into cellular responses during various stimuli.
How is the surgical exposure of the DRG performed?
A carefully delineated incision is made above the lumbar enlargement, allowing access to the L5 DRG while minimizing damage to surrounding tissues.
What types of responses can be observed using this method?
The protocol enables the observation of spontaneous calcium transients and responses to mechanical and thermal stimuli, which are crucial for understanding pain mechanisms.
Can this method be adapted for other types of ganglia?
Yes, the technique can be modified to study trigeminal or geniculate ganglia using genetically encoded sensors for voltage or other signaling molecules.
What are the primary limitations to consider when implementing this method?
The procedure requires extensive practice to ensure precision and minimize complications, and it’s essential to monitor the animal to prevent anesthesia overdosing.

Dieses Protokoll beschreibt die chirurgische Exposition des dorsalen Wurzelganglions (DRG) gefolgt von GCaMP3 (genetisch kodierter Ca2+ Indikator; Grün fluoreszierendes Protein-Calmodulin-M13 Protein 3) Ca2+ Bildgebung der neuronalen Ensembles mit Pirt-GCaMP3 Mäusen unter Anwendung einer Vielzahl von Stimuli auf die ipsilaterale Hinterpfote.

Die Anzahl der Neuronen, die mit dieser Methode überwacht werden, ermöglicht die Erfassung von Neuronennetzwerkdaten, die mit älteren oder anderen Methoden nicht möglich wären. Der Hauptvorteil dieser Technik ist die Möglichkeit, fast 2.000 primäre sensorische Neuronen gleichzeitig zu überwachen und direkt auf Reize zu reagieren, die auf die Hinterpfote angewendet werden. Dieses Verfahren eignet sich besonders gut, um therapeutische Interventionen bei peripherer Allodynie und Schmerzüberempfindlichkeit zu untersuchen.

Diese Methode kann für die Untersuchung von Trigeminus- oder Genikulatganglien angepasst oder mit genetisch kodierten Sensoren für Spannungs- oder Zellsignalmoleküle, wie z. B. zyklisches AMP, verwendet werden. Es braucht Übung, um diese Operation durchzuführen. Sie können an bis zu sechs dorsalen Wurzelganglien an einem einzigen Tier üben.

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