Name: Harvesting and Preparing Drosophila Embryos for Electrophysiological Recording and Other Procedures (Video) | JoVE Journal
Uploaded: 2009-05-20T00:00:00.000+00:00
Duration: 8 min 22 s
Description: Learn to harvest and dissect Drosophila embryos for electrophysiological recording using water polymerizing surgical glue. This method exposes the ventral CNS and neuromusculature for studying developmental neuroscience.

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5 minutes

K.B. is supported by NIH grant GM54544.

Part 1: Equipment and Supplies
<ol>
<li>A good dissection microscope is required for embryo dissections; 40X magnification is suggested, with 25X eye-pieces to maximally increase magnification.</li>
<li>Fine forceps (number 5) are required for manual selection of embryos and devitellinization of embryos.</li>
<li>Equipment to make and modify fine glass needles is required. Pulled-glass needles are required for the dissection. We prefer solid glass for dissection (last longer), but standard thick-walled glass tubing (outer diameter 1-1.5 mm) works as well. Some people use fine tungsten needles, electrolyzed to the desired sharpness in a bath of 1M NaOH using a 10+ Amp autotransformer battery. Sharpened tungsten dissection needles have the benefit that they are relatively resilient and long-lasting. Hollow glass needles (formed similar to patch clamp electrodes) are attached to plastic tubing and used during dissection for suction and expulsion of saline, as well as the controlled delivery of glue. A variety of glass pullers are available for manufacturing glass needles. Computer-programmed pullers can be preset to pull a variety of shapes and sizes. The Brown-Flaming models (Sutter Instrument Co.) are widely favored. A compound microscope (20-40X objective) should be available to inspect and modify electrodes prior to use.</li>
<li>Two types of solutions are commonly used to bath the embryonic tissues during dissection: 1) &ldquo;standard&rdquo; (Jan and Jan, 1976a) or &ldquo;modified standard&rdquo; (Broadie, 2000) salines, based on solutions commonly used for recording in other invertebrate systems, and 2) &ldquo;haemolymph-like&rdquo; (HL) salines (Stewart et al 1994), a compromise between the standard saline and the ionic concentrations measured in the Drosophila haemolymph. It should be noted that none of these salines accurately mimic the chemical composition of haemolymph in vivo (Broadie, 2000). Standard saline contains (in mM): 135 NaCl, 5 KCl, 4 MgCl2, 1.8 CaCl2, 72 sucrose, 5 TES, pH 7.2. Experimenters may also want to consider commercially prepared insect saline (e.g. Schneider&rsquo;s Insect Media), which is unsuitable for electrophysiological recording but most likely to protect the health of exposed tissues.</li>
</ol>
Part 2: Embryo Staging and Dissection
<ol>
<li>For optimal egg collection, maintain young (&lt;7 days), healthy male and female flies (20-40) on fresh laying pots for 2-3 days. Laying pots commonly consist of 100 ml plastic beakers (Tri-Pour) perforated to provide adequate air circulation, covering a 60 mm agar plate. Agar plates contain apple or grape juice hardened with agar. Several recipes exist, but one example is as follows: 700 ml of water, 25-30 grams agar, 300 ml of juice concentrate (grape or apple), 0.5g methyl paraben (p-hydroxymethylbenzoate), and 30g sugar. Autoclave the water and agar, and separately boil the p-hydroxymethylbenzoate with the sugar and juice. Mix the agar and juice solutions and quickly pour into 60 mm plates, removing bubbles.</li>
<li>Prior to egg collection, flies are fed with yeast paste (7 grams baker&rsquo;s yeast in 9 ml of water stored at 4&deg;C) on fresh plates, changed at least twice a day for at least two days. By day 3, a good pot should produce 100-200 eggs per hour. Better egg laying is observed on a pot maintained on its side with the agar in the plate scratched. Many embryos will be laid in or next to the scratches.</li>
<li>To collect large numbers of embryos, gently transfer the embryos from the agar plate into a basket using a paintbrush. A basket can be made with a 15 or 50 ml centrifuge tube. Cut off the bottom leaving enough surface area to trap a screen (70 &micro;m mesh) between the lid and the top of the tube. Rinse the embryos with dH20 and put into a Petri dish of fresh 50% to 100% bleach to remove the outer chorion. Alternatively, eggs can be collected individually using fine forceps, and dechorionated by placing them manually into a drop of bleach. De-chorionation can take from 30 seconds to 2 minutes (fresh bleach is much faster), and should be monitored under the dissection microscope. Removal of the chorion exposes the shiny, transparent vitelline membrane. Dechorionated eggs should be briefly rinsed, or placed in saline, as bleach rapidly destroys devitellinized tissues.</li>
<li>It is critical to carefully stage embryos to the desired developmental age. The defined Drosophila embryonic stages (1-17; Campos-Ortega and Hartenstein, 1985) are not useful, as all functional neuromuscular development occurs in late stage 16 or stage 17. Thus, embryos are staged by developmental hours at 25&deg;C in a humidified incubator, in hours after fertilization or, more commonly, after egg laying (AEL). Under these conditions, embryogenesis lasts 21 +/- 1 hr at 25&deg;C.</li>
<li>Eggs from a timed egg-lay (1-2 hrs) that are appropriately aged are next viewed for morphological criteria. After extensive washing in dH2O, the dechorionated eggs are placed in a plastic culture dish (under dH2O) for viewing. Correct staging can be confirmed with morphological criteria using reflected light with a dissection microscope (Campos-Ortega and Hartenstein, 1985). Mature late-stage embryos (22-24h AEL) on the verge of hatching are generally recognized by segmentation of the cuticle and inflated trachea. Embryos can also be genotyped using GFP balancers and a fluorescence dissection microscope with appropriate filters.</li>
<li>For dissection, dechorionated and developmentally staged embryos are attached (dorsal side up) on a coverslip under a drop of saline (see step 1.5). Embryos are removed from the vitelline membrane by puncturing the membrane near the anterior or posterior end with a glass micropipette or tungsten needle, and then gently freeing the embryo from the membrane. In preparation for dissection, the embryo should be positioned on the coverslip with the dorsal surface up (Dorsal side up dissection will expose the ventral nervous system and neuromusculature for experiments. However, the embryo can obviously be positioned in other ways to facilitate access to other tissues. )</li>
<li>Early stage embryos (&lt;16 hrs AEL) attach directly to clean glass or glass coated with polylysine (poly-L-lysine hydrobromide; Broadie and Bate, 1993a, b). Older embryos (&gt;16 hrs AEL), following cuticle formation, must be glued, ideally to Sylgard-coated (Dow Corning) coverslips. A water-polymerizing cyanoacrylate surgical or veterinary glue is used (Broadie and Bate, 1993c, d). The glue is delivered through a small glass electrode pipette (10-20 micrometer inner diameter tip) attached to a rubber tube with the glue flow controlled by mouth pressure. Care must be taken during glue delivery, as the glue polymerizes quickly upon contacting the saline. Note also that gluing cannot be performed in saline with no or low divalent ion concentrations, as the glue requires divalent ions to polymerize. Small amounts of glue are first used to firmly attach the head and tail.</li>
<li>Once the ends of the embryo are glued to the coverslip, an incision is made along the dorsal midline with a glass electrode or sharpened tungsten needle. This is made easier by gently perforating the line of incision prior to making the final cut. The sides of the incision are then attached to the coverslip with more glue, to gently spread the embryo flat. The internal organs including the gut, fat bodies and, optionally, trachea are then removed by suction using a glass pipette attached to rubber tubing (Broadie and Bate 1993a-c). The embryo should now be attached flat to the coverslip, epidermis down with the ventral central nervous system, peripheral nerves, and somatic musculature exposed for experimentation.</li>
</ol>

Precise staging of embryos is critical due to the rapid maturation of functional properties over the time course of just several hours. Several issues complicate this staging. First, most researchers use timed egg lays to stage embryos, but the egg laying time can vary enormously from animal to animal in different conditions (Broadie et al. 1992). In particular, females on a limited diet tend to retain fertilized eggs for prolonged periods prior to laying. It is therefore critical to &ldquo;clear&rdquo; females by feedin...

<table><tbody><tr><td>Embryo Collection Cages</td><td>Genesee Scientific</td><td>59-100 (for 60 mm dish; other sizes available)</td><td>Cages can also be home made using punctured tri-pour beakers, as shown in video</td></tr><tr><td>Sylgard 184</td><td>Dow Corning</td><td>Available from various companies</td><td>Surgical glue adheres better to sylgard-coated coverslips</td></tr><tr><td>Fine glass tubing, outer diameter 1.0-1.5 mm</td><td>Various</td><td></td><td>For pulling into fine glass needles for dissection and tubes for glue delivery</td></tr><tr><td>Plastic tubing, to attach to glass pipette for mouth suction and glue application</td><td>Tygon</td><td></td><td>Tubing inner diameter needs to match glass outer diameter.</td></tr></tbody></table>

harvesting and preparing drosophila embryos for electrophysiological recording and other procedures

Harvesting and Preparing Drosophila Embryos for Electrophysiological Recording and Other Procedures

Drosophila is a premier genetic model for the study of both embryonic development and functional neuroscience. Traditionally, these fields are quite isolated from each other, with largely independent histories and scientific communities. However, the interface between these usually disparate fields is the developmental programs underlying acquisition of functional electrical signaling properties and differentiation of functional chemical synapses during the final phases of neural circuit formation. This interface is a critically important area for investigation. In Drosophila, these phases of functional development occur during a period of &lt;8 hours (at 25&deg;C) during the last third of embryogenesis. This late developmental period was long considered intractable to investigation owing to the deposition of a tough, impermeable epidermal cuticle. A breakthrough advance was the application of water-polymerizing surgical glue that can be locally applied to the cuticle to enable controlled dissection of late-stage embryos. With a dorsal longitudinal incision, the embryo can be laid flat, exposing the ventral nerve cord and body wall musculature to experimental investigation. This system has been heavily used to isolate and characterize genetic mutants that impair embryonic synapse formation, and thus reveal the molecular mechanisms governing the specification and differentiation of synapse connections and functional synaptic signaling properties.

This technique exposes the Drosophila embryonic neuromusculature for immunohistochemistry or electrophysiological recording. It is useful for studying early events in neuromuscular development or performing electrophysiology in mutants that cannot hatch.

Drosophila is a premier genetic model for the study of both embryonic development and functional neuroscience. Traditionally, these fields are quite ...

To perform electrophysiological recordings in drosophila embryos, they must first be harvested, coordinated, and dissected controlled dissection is made possible with water polymerizing surgical glue, which stabilizes the embryos to cover slips. The internal organs are then removed from stabilized embryos to expose the ventral CNS, the peripheral nerves and the somatic musculature. Hi, I am Dave Featherstone from the Department of Biological Sciences here at the University of Illinois at Chicago.Hi, I'm Ton from the Lab of Dave Featherstone in the Department of Biological Sciences at University of Illinois at Chicago. Today we're going to show you how to collect and manually dissect late stage embryos from Joof. We use this procedure General lab to prepare for electro alternative testing of joof neuromuscular system development and function, which I'll show you another upcoming Jo Ova presentation.So let's get started. This protocol begins with embryo collection, a common procedure used in a variety of joof experiments, which we will now review. Establish a mix of 20 to 40 young male and female flies in a laying pot.House them in a humidified chamber at 25 degrees Celsius. To accurately estimate the developmental stage of the embryo, the temperature and humidity should be consistent. Although commercial laying pots are available, they can be constructed from perforated 100 mil trip poor plastic beakers that fit onto 60 millimeter apple auger plates.The apple auger recipe can be found in the written protocol. Perforations in the beaker can be made with a heated probe and should be smaller than adult flies. The plates are supplemented with a bolus of yeast paste, which will stimulate the females to lay many eggs, mix yeast and water to a peanut butter consistency, and then smear on the plates with a spatula.Change the plate twice daily, Tapping the flies off the plate. And now I can put on a new plate and that can go back to the incubator. But meanwhile, I could check to see how many eggs have been laid here By the third day.A good pot should produce 100 to 200 eggs per hour with the highest egg output between dawn and late morning. To simplify collection, scratch, or chisel origin into the collection plate auger, most eggs will be laid in or next to the scratches for this procedure. The flies are allowed to lay eggs for one to two hours, so late stage embryos can be harvested, but this timeframe will vary depending on the experiment.Embryo collection methods will also vary depending on the number of embryos needed for the experiment. For dissection and electrophysiology, relatively few embryos are needed, in which case they can be picked gently from the plates with fine forceps. To remove the outer corion, rinse the embryos with distilled water and place them in a dish containing fresh 50 to 100%bleach each monitor the embryos under a dissection microscope.After 30 to 120 seconds, the corion will dissolve exposing the shiny transparent vital membrane. Because bleach can rapidly destroy the vitalized tissues, the dechlorinated eggs should be briefly rinsed or placed in saline. Place the dechlorinated eggs in a plastic culture dish containing distilled water.At this time, they can be visually genotyped by checking for GFP markers with a fluorescence dissection microscope, and appropriate filters after sorting out the of interest, proceed with the dissection. Because embryos are too small for dissection pins, some advanced preparation is required. Older embryos with developed cuticles must be glued to sogar coated cover slips using cyanoacrylate surgical or veterinary glue cyanoacrylate surgical glue, also known as histo aal.Blue works well because it polymerizes in contact with solution containing divalent ions. Begin the dissection by transferring an embryo of interest to a cigar coated cover slip under a drop of saline with its dorsal side up. Remove the vital membrane by making a small incision in the membrane with a glass micro pipette or a tungsten needle.Then gently free the embryo from the membrane. Early stage embryos will attach directly to clean glass or glass coated with poly L lysine. For older embryos, attach them to sard coated cover slips by delivering surgical glue through a small glass pipette attached to a rubber tube.The glue flow is controlled by mouth. Use small amounts of glue to firmly attach the head and tail. Do this carefully because the glue mizes quickly in the saline.To dissect the stabilized embryo, gently perforate a line along the dorsal midline with a glass electrode or a sharpened tungsten needle. Using the same tool make an incision by cutting through the perforations. It is critical that the dissection needle is always at a shallow angle to avoid damaging the ventral neuro musculature.Next, remove the internal organs using gentle mouth suction from a glass pipette attached to rubber tubing. Spread the embryo flat by using more glue to attach the sides of the incision to the cover slip. Once all the internal organs are vacuumed away, the ventral CNS peripheral nerves and somatic musculature are exposed for experimentation.At this point, the embryo is ready for electrophysiological recordings or it can be fixed for immunohistochemistry and subsequent microscopy using conventional techniques. We've just shown you how to isolate and dissect the later stage to softener embryos. The application of surgical glue and dissection of the embryos will be frustrating at first, but there are no secret tricks.You've gotta develop the fine motor skills with practice over several weeks, but gradually the percentage of successful dissections will increase. Please have a look at our other geo video, which details recording configurations from muscle cells and the motor neurons. So that's it.Thanks for watching and good luck with your experiments.

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Learn to harvest and dissect Drosophila embryos for electrophysiological recording using water polymerizing surgical glue. This method exposes the ventral CNS and neuromusculature for studying developmental neuroscience.

Harvesting and Preparing Drosophila Embryos for Electrophysiological Recording and Other Procedures

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