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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.
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.
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
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.......
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.......
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.......
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).
....Name | Company | Catalog Number | Comments |
4',6-diamidino-2-phenylindole dihydrochloride | ThermoFisher | D3571 | |
Confocal laser scanning microscope | Olympus | FV1200 | |
Donkey anti-chicken AF488 | Jackson | 149973 (703-545-155) | |
Donkey anti-goat AF546 | ThermoFisher | A11056 | |
Donkey anti-rabbit AF488 | ThermoFisher | A21206 | |
Donkey anti-rabbit AF546 | ThermoFisher | A10040 | |
Frozen Section Medium | ThermoFisher | Neg-50 | Colorless |
Microscope cover glass | Citotest | 10212450C | |
Microtome | Yamato | REM-710 | |
Neurofilament 200 | Sigma-Aldrich | N4142 | Rabbit |
Neurofilament 200 | Abcam | ab4680 | Chicken |
Normal donkey serum | Jackson ImmunoResearch Laboratories | 017-000-12 | 10 ml |
Normal saline | Shandong Hualu Pharmaceutical Co.Ltd | H37022750 | 250 ml |
Paraformaldehyde | Macklin | P804536 | 500g |
Phalloidin AF350 | ThermoFisher | A22281 | |
Precision peristaltic pump | Longer | BT100-2J | |
S100-β | Abcam | ab52642 | Rabbit |
Sodium phosphate dbasic dodecahydrate | Macklin | S818118 | 500g |
Sodium phosphate monobasic dihydrate | Macklin | S817463 | 500g |
Sucrose | Macklin | S818046 | 500g |
Superfrost plus microscope slides | ThermoFisher | 4951PLUS-001E | |
Triton X-100 | Solarbio Life Sciences | 9002-93-1 | 100 ml |
Vesicular Acetylcholine Transporter | Milipore | ANB100 | Goat |
α-bungarotoxin AF647 conjugate | ThermoFisher | B35450 |
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