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Neuroscience
頭蓋挙筋長耳骨格筋の In vivo エレクトロポレーションと短期再神経支配の組み合わせ
頭蓋挙筋長耳骨格筋の In vivo エレクトロポレーションと短期再神経支配の組み合わせ
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JoVE Journal Neuroscience
Combined In Vivo Electroporation and Short-Term Reinnervation of the Cranial Levator Auris Longus Skeletal Muscle

頭蓋挙筋長耳骨格筋の In vivo エレクトロポレーションと短期再神経支配の組み合わせ

Full Text
961 Views
04:44 min
November 1, 2024

DOI: 10.3791/66706-v

Jessica Mella*1, Francisca Bermedo-Garcia*1, Angelymar Medina-Moreno1, Jorge Ojeda2, Juan Pablo Henríquez1,3

1Neuromuscular Studies Lab (NeSt Lab), Institute of Anatomy, Histology, and Pathology, Faculty of Medicine,Universidad Austral de Chile, 2Faculty of Odontology and Rehabilitation Sciences,Universidad San Sebastian, 3Department of Cell Biology, Faculty of Biological Sciences,Universidad de Concepcion

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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 using in vivo electroporation and denervation of the cranial levator auris longus (LAL) muscle to investigate muscle-derived proteins' roles in neuromuscular synapse regeneration. By examining the effects of specific proteins, this protocol aims to elucidate mechanisms underlying the stabilization of postsynaptic acetylcholine receptors and to explore the implications for regenerative processes.

Key Study Components

Area of Science

  • Neuroscience
  • Regenerative Biology
  • Molecular Mechanisms

Background

  • The neuromuscular junction is crucial for muscle contraction and is affected by various cellular signaling events.
  • Understanding the regeneration of neuromuscular synapses can provide insights into recovery from nerve injuries.
  • Muscle-derived proteins may influence the organization and stability of synapses during this process.
  • Previous studies have not fully addressed the role of specific muscle proteins in synaptic regeneration.

Purpose of Study

  • To evaluate the impact of inhibiting or overexpressing specific muscle-derived proteins on neuromuscular junction regeneration.
  • To establish a minimally invasive protocol for studying the regeneration process.
  • To analyze the morphological changes in postsynaptic domains post-denervation.

Methods Used

  • The study utilizes in vivo electroporation for gene transfer in the LAL muscle of anesthetized CF-1 mice.
  • Denervation of the LAL muscle is performed to study the impacts on postsynaptic receptor organization.
  • The protocol involves using electrical pulses for effective gene transfer, with post-procedure recovery and monitoring.
  • Microscopic examination and confocal imaging are conducted to analyze neuromuscular junction denervation.

Main Results

  • The electroporation technique achieved high expression rates of the tagged protein in muscle fibers.
  • Denervation led to identifiable morphological changes in postsynaptic domains, correlated with stability outcomes.
  • Future studies will address aging and neurodegenerative conditions such as ALS by assessing muscle-derived proteins.

Conclusions

  • This study demonstrates a novel approach to understanding the influence of muscle-derived proteins on synaptic stability and regeneration.
  • The outlined methods may serve as foundational steps toward more complex genetic and therapeutic endeavors.
  • Insights gained could significantly impact the understanding of neuromuscular junction dynamics in health and disease contexts.

Frequently Asked Questions

What are the advantages of using in vivo electroporation?
In vivo electroporation allows for targeted gene transfer directly into muscle tissues with a high success rate, resulting in effective expression of proteins for research.
How is denervation of the LAL muscle conducted?
Denervation is achieved via a surgical approach that involves external incision and careful exposure of the nerve for precise crushing without damaging surrounding tissues.
What types of data are obtained from this study?
The study provides data on the expression of muscle-derived proteins, the organization of postsynaptic acetylcholine receptors, and insights into synaptic stability post-denervation.
How can the methods used in this study be adapted?
The protocols can be adapted for various muscle types or different animal models to study distinct regeneration processes or therapeutic interventions.
What are the limitations of this approach?
While minimally invasive, the surgical procedures require expertise and may introduce variability in outcomes due to individual animal responses.
How does this research contribute to understanding diseases like ALS?
Understanding muscle-derived protein roles in synapse regeneration can inform therapeutic strategies for neurodegenerative diseases, potentially improving recovery outcomes.

ここでは、頭蓋長耳挙筋 (LAL) の in vivo エレクトロポレーションと除神経を組み合わせたプロトコルを紹介します。この手順により、神経筋シナプスの再生における筋由来タンパク質の潜在的な役割の研究が可能になります。

私たちの研究は、神経筋シナプスの反復の根底にあるメカニズムを理解し、特定の筋肉由来タンパク質を阻害または過剰発現することがこの再生プロセスに与える影響を評価することを目的としています。筋肉のin vivoエレクトロポレーションを通じて、筋肉由来タンパク質がシナプス後アセチルコリン受容体の組織に与える影響を観察しました。さらに、私たちの除神経プロトコルにより、シナプス後ドメインのさまざまな形態を特定し、それらをそれらの安定性と関連付けることができました。

この技術は、特定の筋タンパク質の生成の影響を評価するための最初の実験的アプローチとして機能し、より複雑な遺伝子編集技術への道を開きます。さらに、これらのプロトコルは低侵襲です。この実験方法の組み合わせは、Wntシグナル伝達またはNMJ再生の役割を調査するために採用されています。

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In vivoエレクトロポレーション 長頭蓋挙筋 神経筋接合部 NMJ維持 筋肉由来タンパク質 遺伝子導入戦略 除神経 機械的神経損傷 神経伝達 顔面神経 筋タンパク質過剰発現 NMJ再神経支配 実験的戦略

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