Name: Drosophila Larval NMJ Dissection (Video) | JoVE Journal
Uploaded: 2009-02-04T00:00:00.000+00:00
Duration: 6 min 42 s
Description: Learn Drosophila larval NMJ dissection for neuroscience research using third instar larvae. This standardized protocol enables clear neuromuscular junction visualization for immunohistochemistry and imaging studies.

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5 minutes

Before you start
<ol>
<li>All cultures should be grown at 25&deg; C.</li>
<li>HL3.1 dissection buffer may be prepared in advance. Take a 50 ml aliquot of HL3.1 and keep it on ice.</li>
<li>Prepare 15 ml of fresh 3.5% Formaldehyde in HL3.1. Keep it on ice.</li>
</ol>
Larval Dissection
<ol>
<li>Put a drop of cold HL3.1 on the dissection plate. This will keep the animal from drying and stun the animal making it easier to work with.</li>
<li>Using the long forceps, select a wandering third instar larva and place it in the drop of HL3.1.</li>
<li>First, use short forceps to grasp a minutien pin. Place the pin between the posterior spiracles. The animal will usually try to crawl away from the pin stretching itself out and making it easier for you to place a pin squarely in the head of the larva near the mouth hooks. Stretch the animal out lengthwise. This will help you maximize the amount of exposed body wall you can achieve during cutting. Note : If you choose to pin the head first, the animal may wrap its body around the pin or whip its body back and forth making it difficult to pin. You can usually counter this by removing the HL3.1 and putting a fresh cold drop stunning the animal again. The ambidextrous scientist can also just grab the animal and hold it in place.</li>
<li>Using spring scissors make a horizontal incision just anterior to the posterior pin on the dorsal side of the larva. Place one blade of the scissors into the incision and make a vertical cut along the dorsal midline toward the rostral end of the larva. At the rostrum of the animal make horizontal incisions to the left and right of the pin. Note: the finished result should look like an I on the dorsal side of the larva along the rostrocaudal axis.</li>
<li>Remove the organs. Begin by putting several additional drops of HL3.1 on the larva. This will enable the organs to float up out of the body allowing you to remove them much more easily. First, remove the tracheal system. Second, use the forceps to grab the rest of the organs and remove them.</li>
<li>During step 3 you made a left flap and right flap in the body wall. Pin the flaps in a clockwise order making sure to stretch the body wall both horizontally and vertically.</li>
</ol>
Fixation
Fix each animal in 3.5% formaldehyde in HL3.1 for 25 minutes. Wash the animal twice in HL3.1 for 5 minutes.
Storage
Remove the pins and transfer the larvae to a 1.5 ml tube containing 1X PBS. If you plan to image the NMJ using fused fluorescent tags, you should image the animals within two days. You may store the dissected larvae for up to one week at 4&deg;C.
Representative results
There are several key components to a properly dissected Drosophila larva. First, one must take extra care not to damage the muscles, especially muscles 4, 6, and 7. These are the most popular muscles to study and if they are damaged discard the fillet prep and dissect another animal. Second, one must make sure that the animal is maximally stretched so that each muscle and NMJ can be distinguished.

<ol><li>Jan, L. Y., Jan, Y. N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Properties+of+the+larval+neuromuscular+junction+in+Drosophila+Melanogaster%5BTitle%5D)+AND+%22J.+Physiol%22%5BJournal%5D)">Properties of the larval neuromuscular junction in Drosophila Melanogaster.</a> J. Physiol. 262, 189-214 (1976).</li>
<li>Johansen, J., Halpern, M. E., Johansen, K. M., Keshishian, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Stereotypic+morphology+of+glutamatergic+synapses+on+identified+muscle+cells+of+Drosophila+larvae%5BTitle%5D)+AND+%22J+Neurosci%22%5BJournal%5D)">Stereotypic morphology of glutamatergic synapses on identified muscle cells of Drosophila larvae.</a> J Neurosci. 9, 710-725 (1989).</li>
<li>Kesheshian, H., Broadie, K., Chiba, A., Bate, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+Drosophila+neuromuscular+junction%3A+a+model+system+for+studying+synaptic+development+and+function%5BTitle%5D)+AND+%22Annu+Rev+Neurosci%22%5BJournal%5D)">The Drosophila neuromuscular junction: a model system for studying synaptic development and function.</a> Annu Rev Neurosci. 19, 545-575 (1996).</li>
<li>Vactor, D. V., Sink, H., Fambrough, D., Tsoo, R., Goodman, C. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Genes+that+control+neuromuscular+specificity+in+Drosophila%5BTitle%5D)+AND+%22Cell%22%5BJournal%5D)">Genes that control neuromuscular specificity in Drosophila.</a> Cell. , 73-1137 (1993).</li>
<li>Feng, <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+modified+minimal+hemolymph-like+solution%2C+HL3.1%2C+for+physiological+recordings+at+the+neuromuscular+junctions+of+normal+and+mutant+Drosophila+larvae%5BTitle%5D)+AND+%22J+Neurogenet%22%5BJournal%5D)">A modified minimal hemolymph-like solution, HL3.1, for physiological recordings at the neuromuscular junctions of normal and mutant Drosophila larvae.</a> J Neurogenet. 18 (2), 377-402 (2004).</li>
</ol>

The dissection technique demonstrated in this video can be used to prepare Drosophila larvae for a variety of experimental techniques. If fluorescent protein tags are present, the larvae can be mounted and imaged immediately. Otherwise, immunostaining can be performed in order to mark specific synaptic compartments. In addition, electrophysiology can easily be performed on the dissected larvae to evaluate the functioning of neurotransmission.
The NMJ of Drosophila has gained...

<table><tbody><tr><td>Stereomicroscope &amp;#8220;Stemi&amp;#8221; 2000</td><td>Carl Zeiss, Inc.</td><td>495101-9804-000</td><td></td></tr><tr><td>Light Source KL 1500 LCD</td><td>Carl Zeiss, Inc.</td><td>000000-1063-181</td><td></td></tr><tr><td>3mm Vannas Spring Scissors</td><td>Fine Science Tools</td><td>15000-0</td><td></td></tr><tr><td>Dumont SS Forceps</td><td>Fine Science Tools</td><td>11200-33</td><td>Long forceps</td></tr><tr><td>Dumont #5 Forceps</td><td>Fine Science Tools</td><td>11252-20</td><td>Short forceps</td></tr><tr><td>SylGard 182 Silicone Elastomer Kit</td><td>Dow Corning</td><td>3097358-1004</td><td>Used to make dissection plates</td></tr><tr><td>Formaldehyde </td><td>Sigma-Aldrich</td><td>252549-25ML</td><td></td></tr><tr><td>Stainless Steel Minutien Pins -0.1 MM Diameter</td><td>Fine Science Tools</td><td>26002-10</td><td></td></tr><tr><td colspan="4">HL3 Dissection Buffer: (in mM) 70 NaCl, 5 KCl, 0.2 CaCl2, 20 MgCl2, 10 NaHCO3, 5 trehalose, 115 sucrose, and 5 HEPES, pH 7.3.&lt;br/&gt;&lt;br/&gt;Sylgard Dissecting Plate: Mix gently (to avoid bubbles) 10:1in a beaker. Pour mixture into Petri dish (any size). Allow SylGard to cure overnight in 37C incubator.</td></tr><tr><td colspan="4">&lt;br/&gt;&lt;br/&gt;Sylgard Dissecting Plate: Mix gently (to avoid bubbles) 10:1in a beaker. Pour mixture into Petri dish (any size). Allow SylGard to cure overnight in 37C incubator.</td></tr><tr><td colspan="4">&lt;br/&gt;Sylgard Dissecting Plate: Mix gently (to avoid bubbles) 10:1in a beaker. Pour mixture into Petri dish (any size). Allow SylGard to cure overnight in 37C incubator.</td></tr><tr><td colspan="4">Sylgard Dissecting Plate: Mix gently (to avoid bubbles) 10:1in a beaker. Pour mixture into Petri dish (any size). Allow SylGard to cure overnight in 37C incubator.</td></tr></tbody></table>

drosophila larval nmj dissection

Drosophila Larval NMJ Dissection

The Drosophila neuromuscular junction (NMJ) is an established model system used for the study of synaptic development and plasticity. The widespread use of the Drosophila motor system is due to its high accessibility. It can be analyzed with single-cell resolution. There are 30 muscles per hemisegment whose arrangement within the peripheral body wall are known. A total of 35 motor neurons attach to these muscles in a pattern that has high fidelity. Using molecular biology and genetics, one can create transgenic animals or mutants. Then, one can study the developmental consequences on the morphology and function of the NMJ. In order to access the NMJ for study, it is necessary to carefully dissect each larva. In this article we demonstrate how to properly dissect Drosophila larvae for study of the NMJ by removing all internal organs while leaving the body wall intact. This technique is suitable to prepare larvae for imaging, immunohistochemistry, or electrophysiology.

This protocol demonstrates how to dissect Drosophila larvae in preparation for immunohistochemistry and/or imaging of the neuromuscular junction.

The Drosophila neuromuscular junction (NMJ) is an established model system used for the study of synaptic development and plasticity. The widespread use ...

This procedure begins with placing a third instar larvae on the dissection plate. Pins are placed in the posterior and anterior ends of the larvae. Scissors are used to cut the larvae open and forceps are used to remove the internal organs.Finally, four more pins are placed in each corner of the larva body wall to hold it taut during fixation. Hi, I'm Jonathan Brent from the Laboratory of Brian McCabe in the Department of Physiology and solo biophysics at Columbia University College of Physicians and Surgeons. Today we'll show you the procedure for drosophila larva and MJ dissection.We use this procedure in our laboratory to study neuromuscular junction synaptic development. So let's get started. In drosophila larvae, there are 30 muscles per hemi segment whose arrangement within the peripheral body wall are known.A total of 35 motor neurons innervate these muscles in a highly stereotyped pattern. To access the neuromuscular junction or NMJ, it is necessary to carefully dissect each larva with proper dissection. The NMJ may be used for imaging immunohistochemistry or electrophysiology.Begin the procedure by putting a drop of HL 3.1 buffer onto a dissection plate. The buffer is made in advance and cooled on ice. Carefully pick a wandering third end star larvae from the side of the vial using large SS forceps.The movement indicates that the larvae has not entered Pupation Place the larvae dorsal side up in the buffer drop on the dissection plate. The cold buffer will anesthetize the larvae and keep it still using forceps. Place a mnuchin pin between the posterior sphericals, then place a second pin close to the dark mouth hooks so that the larvae is stretched out and ready to splay open.Using spring scissors, make a small horizontal incision toward the posterior end of the larvae. Insert one blade of the scissors into the sci and make a lengthwise cut toward the anterior end of the larva. Then, then make horizontal incisions at the anterior end of the larvae to the left and to the right of the pin.To remove organs such as the gut, add several drops of HL 3.1 buffer to the animal, the gut and other organs will float up into the solution and they can be pulled away from the body using forceps. Also, remove the tracheal system with the other organs. Now expose the interior body muscles by pinning back the flaps made by the incisions.Be sure to stretch the body walls open horizontally and vertically. When pinning down the flaps. Remove any remaining organ pieces and wash once.By adding fresh HL 3.1 buffer, the larva is now ready to be fixed with freshly made formaldehyde diluted to 3.5%in one XPBS completely immerse the larvae and fixative and wait 25 minutes. When the fixation period is over, wash the larvae twice with HL 3.1 buffer for three minutes. Carefully remove the pins, Transfer the larvae to 1.5 mil tubes containing one XPBS if needed.The larvae can be stored for up to two days at four degrees Celsius. For optimal results, use the dissected larvae immediately. There are several key components to a properly dissected drosophila larva.First, be careful to not damage the muscles, especially six, seven, and four. Second, the animal must be properly stretched out. Otherwise, the neuromuscular junction may not be accessible or distinguishable.Here you can see a properly dissected larva. The NMJ is clearly visible and the system is now ready for experiments. We've just shown you how to dissect esophagal larva to study the neuromuscular junction.When doing this procedure, it's important to lead the muscles intact. If the muscles are damaged, there will be no neuromuscular junctions to study. So that's it.Thanks for watching and good luck with your experiments.

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Learn Drosophila larval NMJ dissection for neuroscience research using third instar larvae. This standardized protocol enables clear neuromuscular junction visualization for immunohistochemistry and imaging studies.

Drosophila Larval NMJ Dissection

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