Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The protocol shows a method to examine spatial correlation among the pre-synaptic terminals, post-synaptic receptors, and peri-synaptic Schwann cells in the rat medial gastrocnemius muscle using fluorescent immunohistochemistry with different biomarkers, namely, neurofilament 200, vesicular acetylcholine transporter, alpha-bungarotoxin, and S100.

Abstract

The neuromuscular junction (NMJ) is a complex structure serving for the signal communication from the motor neuron to the skeletal muscle and consists of three essential histological components: the pre-synaptic motor axon terminals, post-synaptic nicotinic acetylcholine receptors (AchRs), and peri-synaptic Schwann cells (PSCs). In order to demonstrate the morphological characteristics of NMJ, the rat medial gastrocnemius muscle was selected as the target-tissue and examined by using multiple fluorescent staining with various kinds of biomarkers, including neurofilament 200 (NF200) and vesicular acetylcholine transporter (VAChT) for the motor nerve fibers and their pre-synaptic terminals, alpha-bungarotoxin (α-BTX) for the post-synaptic nicotinic AchRs, and S100 for the PSCs. In this study, staining was performed in two groups: in the first group, samples were stained with NF200, VAChT, and α-BTX, and in the second group, samples were stained with NF200, α-BTX, and S100. It was shown that both protocols can effectively demonstrate the detailed structure of NMJ. Using the confocal microscope, morphological characteristics of the pre-synaptic terminals, post-synaptic receptors, and PSC were seen, and their Z-stacks images were reconstructed in a three-dimensional pattern to further analyze the spatial correlation among the different labeling. From the perspective of methodology, these protocols provide a valuable reference for investigating the morphological characteristics of NMJ under physiological conditions, which may also be suitable to evaluate the pathological alteration of NMJ, such as peripheral nerve injury and regeneration.

Introduction

As three essential structural components of the neuromuscular junction (NMJ)1,2,3,4, morphological aspects of the pre-synaptic motor axon terminals, post-synaptic membrane containing nicotinic acetylcholine receptors (AchRs), and peri-synaptic Schwann cells (PSCs) have extensively been investigated. Thin sections and whole-mount specimens of the skeletal muscles have been examined with different histological techniques, such as electron microscopy5,6, confocal microscopy

Protocol

This study was approved by the Ethics Committee of Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences (approval No. 2021-04-15-1). All procedures were conducted in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals (National Academy Press, Washington, D.C., 1996). Three adult male rats (Sprague-Dawley, weight 230 ± 15 g) were used. The rats were housed in a 12 h light/dark cycle with controlled temperature and humidity and with free acc.......

Representative Results

After multiple fluorescent staining, the corresponding labeling was orderly demonstrated on the 80 µm thick sections of the rat medial gastrocnemius muscle with NF200-positive nerve fibers, VAChT-positive pre-synaptic terminals, α-BTX-positive post-synaptic AchRs, S100-positive PSCs, phalloidin-positive muscular fibers, and DAPI-labeled cellular nuclei (Figure 3 and Figure 4).

It was shown that NF200-positive nerve fibers ra.......

Discussion

We have described the technical details required for performing successful multiple staining of muscle slices and use of fluorescent immunohistochemistry for revealing the morphological characteristics of NMJ on the thick sections of the rat medial gastrocnemius muscle. By using this approach, the fine details and spatial correlation of the PSCs and pre- and post-synaptic elements can be analyzed and appreciated under confocal microscopy, and further reconstructed in a three-dimensional pattern. Here, various kinds of bi.......

Acknowledgements

This study was funded by the CACMS Innovation Fund (No. CI2021A03407), National Natural Science Foundation of China (No. 82004299), and the Fundamental Research Funds for the Central Public Welfare Research Institutes (No. ZZ13-YQ-068; ZZ14-YQ-032; ZZ14-YQ-034; ZZ201914001; ZZ202017006; ZZ202017015).

....

Materials

NameCompanyCatalog NumberComments
4',6-diamidino-2-phenylindole dihydrochlorideThermoFisherD3571
Confocal laser scanning microscopeOlympusFV1200
Donkey anti-chicken AF488Jackson149973 (703-545-155)
Donkey anti-goat AF546ThermoFisherA11056
Donkey anti-rabbit AF488ThermoFisherA21206
Donkey anti-rabbit AF546ThermoFisherA10040
Frozen Section MediumThermoFisherNeg-50Colorless
Microscope cover glassCitotest10212450C
MicrotomeYamatoREM-710
Neurofilament 200Sigma-AldrichN4142Rabbit
Neurofilament 200Abcamab4680Chicken
Normal donkey serumJackson ImmunoResearch Laboratories017-000-1210 ml
Normal salineShandong Hualu Pharmaceutical Co.LtdH37022750250 ml
ParaformaldehydeMacklinP804536500g
Phalloidin AF350ThermoFisherA22281
Precision peristaltic pumpLongerBT100-2J
S100-βAbcamab52642Rabbit
Sodium phosphate dbasic dodecahydrateMacklinS818118500g
Sodium phosphate monobasic dihydrateMacklinS817463500g
SucroseMacklinS818046500g
Superfrost plus microscope slidesThermoFisher4951PLUS-001E
Triton X-100Solarbio Life Sciences9002-93-1100 ml
Vesicular Acetylcholine TransporterMiliporeANB100Goat
α-bungarotoxin AF647 conjugateThermoFisherB35450

References

  1. Kawabuchi, M., et al. The spatiotemporal relationship among Schwann cells, axons and postsynaptic acetylcholine receptor regions during muscle reinnervation in aged rats. TheAnatomical Record. 264 (2), 183-202 (2001).
  2. Nishimune, H., Shigemoto, K.

Explore More Articles

Neuromuscular JunctionMedial Gastrocnemius MuscleRatMorphological CharacteristicsSchwann CellsPre synapticPost synapticImmunofluorescencePerfusionCryoprotectionCryosectioningTriton X 100Normal Donkey SerumNeurofilament 200Vesicular Acetylcholine TransporterDonkey Anti rabbit AF 488Donkey Anti goat AF 594

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved