This work was supported by grants from the National Institutes of Health R03 AG061484-02 and the UMBC College of Natural and Mathematical Sciences Becton Dickinson Faculty Research Fund.

1. Collect and age Drosophila
<ol>
	<li>To generate same aged F1 flies for testing phagocytosis, add 5-10 virgin females and 5 males of the appropriate genotypes to a vial containing fresh fly food. We use a cornmeal molasses agar based food20, but the method should work regardless of the type of diet the flies are reared on. For this experiment we used Hemese (He)-GAL4; UAS-GFP flies to label hemocytes genetically. 
	NOTE: More flies can be used, but some lines of D. melanogaster may not mate or reproduce well when overcrowded, and overcrowding may have adverse effects on larval development21 and phagocytosis.</li>
	<li>Maintain flies under the desired experimental conditions. For this experiment, maintain He-GAL4; UAS-GFP flies at 24 &#176;C. Allow adult flies to mate for a week, and then remove adults. F1 flies will then be collected from these vials after eclosion for experimental use.&#160;</li>
	<li>Collect virgin flies throughout the week, or until the desired number of flies are collected. Virgins are not required; however, mating may impact immune response. If F1 flies are to be tested as virgins, separate males and females within 8 hours of eclosion and maintain in separate vials to prevent mating. Collect enough flies to allow assessment of phagocytosis in at least 10 flies per genotype/treatment/sex per age.
	<ol>
		<li>If aging the flies to one week, collect at least 50 flies total, or 20 flies per treatment condition for each particle, either fluoro-particles or pH sensitive particles, to be injected. This will ensure a minimum of 10 flies to assay at the time of the experiment.</li>
		<li>If aging flies to more than 3 weeks, collect at least 100-150 flies total, or 50-75 flies per treatment condition to ensure there are enough flies available to measure phagocytosis. When aging flies in the laboratory, we typically use insect cages maintained at 24 &#176;C in 12:12 L:D conditions, and change the food every other day. If vials are being used instead of cages, tip flies into new vials every 3-5 days, depending on the condition of the food in the vial. The number of flies needed will depend on how late in age phagocytosis will be analyzed, and the age-specific survival rates of that genotype in a particular environmental condition.</li>
		<li>If young and aged flies will be assessed, plan accordingly so that 1-week old and aged flies will be injected on the same day. This will minimize variations in particle concentration between experiments and will ensure that the effect of age on the phagocytic measurement is not confounded with the effect of the day the assay was performed.</li>
	</ol>
	</li>
	<li>House the collected flies at 24 &#176;C until they are 5-7 days old, or maintain the flies to the desired age.</li>
</ol>
2. Prepare fluorescently labeled particles
<ol>
	<li>Reconstitute heat-killed E. coli fluoro-particles or pH sensitive E. coli particles to a stock concentration of 20 mg/mL or 1 mg/mL, respectively. Other bacteria are available for use that may be more suitable for certain experiments, but refer to the manufacturer&#8217;s instructions for appropriate stock concentrations.
	<ol>
		<li>For fluoro-particles, add 990 &#181;L of 1x PBS (pH 7.4) or preferred buffer and 10 &#181;L of 2 mM (20%) sodium azide. Vortex to mix. 
		NOTE: Sodium azide is a preservative that may be omitted; however, particles prepared without sodium azide do not last as long. Fluoro-particles must be used within 24 hours and pH sensitive particles must be used within 7 days.</li>
		<li>For pH sensitive particles, add 1,980 &#181;L of 1x PBS (pH 7.4) or preferred buffer and 20 &#181;L of 2 mM (20%) sodium azide. Vortex to mix.</li>
		<li>Make multiple single-use 20 &#181;L aliquots in 1.5 mL microcentrifuge tubes. Store fluoro-particles at -20 &#176;C for up to a year, and pH sensitive particles at 4 &#176;C for up to 6 months, protected from light.</li>
	</ol>
	</li>
	<li>On the day of injections, remove sodium azide from the particles before use. To do this, centrifuge the particles for 5 min at 15,000 x g at room temperature.</li>
	<li>Remove the supernatant and wash particles twice by resuspending in 50 &#181;L of 1x PBS or preferred buffer, and centrifuge for 5 min at 15,000 x g.</li>
	<li>After the second wash, remove the supernatant and resuspend particles in 100 &#181;L of 1x PBS or preferred buffer. Keep the solution in the tube and minimize exposure to light throughout the experiment. Once the sodium azide is removed, use fluoro-particles within 24 h, and use pH sensitive particles used within 5-7 days. 
	NOTE: In our previous experiments, we found that this concentration of particles provided countable numbers of phagocytic events and that the number of particles available for phagocytosis by hemocytes was not limiting17. However, users of this protocol may want to compare results using other concentrations to ensure that there is an adequate number of particles available for phagocytosis by hemocytes in the conditions of their experiments.
	<ol>
		<li>If sodium azide was omitted, dilute the particles 1:5 in the same buffer the particles were prepared with, for injections.</li>
	</ol>
	</li>
	<li>Add a drop (~10 &#181;L) of green food coloring to the particles. This makes it easier to ensure the flies have been injected.</li>
</ol>
3. Inject the flies
<ol>
	<li>Prepare glass needles for injections.
	<ol>
		<li>Pull glass needles using a pipette puller. Set the pipette puller heater to 55 &#176;C and the solenoid to 45. Use only the needles provided with the injector, as it is not guaranteed that other needles will work with the same precision.</li>
		<li>Fill a 1 mL sterile syringe with mineral oil, and attach the 30 gauge hypodermic (G) needle, provided with the nano-injector.</li>
		<li>Backfill the pulled capillary needle by inserting the 30 G needle into the blunt end of the pulled glass needle and fill with mineral oil. Slowly remove the 30 G needle, ensuring there are no air bubbles throughout the needle, as this can cause inaccurate injection volumes. The injector will not work properly without backfilling the needle.</li>
		<li>Using forceps, break off the tip of the needle to create an opening to allow ejection of solution.</li>
	</ol>
	</li>
	<li>Assemble the nano-injector. 
	NOTE: Other injectors can be used. The method described below apply to the nano-injector. For other injectors, consult the user manual for instructions.
	<ol>
		<li>Set the injector to the desired volume (between 46 nL and 69 nL).</li>
		<li>Remove the collet and place the sealing O-ring, the white spacer with the indentation facing up to receive the back end of the needle, and the larger O-ring onto the metal plunger, in that order. Reattach the collet without tightening it.</li>
		<li>Insert the metal plunger into the blunt end of the oil-filled glass needle. Gently push the needle down, inserting it into the larger O-ring. Tighten collet until secure. 
		NOTE: If the metal plunger does not extend past the collet, press and hold &#8216;EMPTY&#8217; until the plunger is visible. This makes it easier to ensure the plunger is inserted into the needle.</li>
		<li>Press and hold &#8216;EMPTY&#8217; until the injector beeps. This ejects most of the mineral oil from the needle, leaving a small volume of oil to act as a barrier between the two liquids, as well as removes air bubbles.</li>
		<li>Fill the needle with either fluoro-particles or pH sensitive particles by inserting the tip of the glass needle into the microcentrifuge tube containing the prepared particles.</li>
		<li>Press and hold &#8216;FILL&#8217; until the injector beeps.</li>
	</ol>
	</li>
	<li>Injections
	<ol>
		<li>Transfer the flies that are to be injected into an empty vial. Immobilize the flies by placing the vial in ice. CO2 can also be used to immobilize the flies. However, note that, when using pH sensitive particles, elevated CO2 levels can artificially acidify any buffers being used and can elevate background fluorescence.</li>
		<li>Inject the flies in the sternopleural plate of the thorax (Figure 1A). The injection is successful if green dye is seen going into the fly (Figure 1B). If the fly does not turn green, make sure the needle is not clogged. 
		NOTE: Alternatively, flies can be injected in the abdomen, but keep the injection site consistent across all experiments.</li>
		<li>Place injected flies into a new food vial, noting the time that the first and last fly was injected. To minimize experimental error due to the amount of time it takes to complete injections, complete injections in a timely manner. With practice, it should take no longer than 10 min to inject one set of flies. Lay the vial on its side until all of the flies have recovered, to prevent the flies from becoming stuck in the food.</li>
		<li>Allow flies to recover for 60-90 min, depending on experimental conditions. Here, a 60-min recovery time was used. Note that this recovery time range was optimal for counting phagocytic events in the experimental conditions in the Horn et al. study17. However, under some conditions, this may be too long to detect subtle differences in phagocytosis between treatment groups. It may be useful to carry out time course experiments as was done previously17 to determine the recovery time that will reveal maximal differences between control and experimental results. Whatever recovery time is chosen, keep this consistent across all experimental treatments.</li>
		<li>If injecting with fluoro-particles and pH sensitive particles on the same day, use a new needle for each solution. Do not inject individual flies with both particles if they both fluoresce red, since the result would not differentiate between the two aspects of phagocytosis, particle binding/engulfment vs. particle inclusion in the phagosome.</li>
	</ol>
	</li>
</ol>
4. Dissecting the dorsal vessel
<ol>
	<li>After flies have recovered for 60-90 min, transfer all living flies to an empty vial and immobilize on ice.</li>
	<li>Transfer one fly at a time onto a silicone elastomer dissection plate. 
	NOTE: Prepare dissection plates at least 1-week prior to use, if curing at room temperature. To do this, prepare the elastomer and pour it into a 33 mm x 10 mm Petri dish, filling the dish about halfway. Gently tap the dish on a flat surface to minimize air bubbles. Let the plates sit at room temperature, undisturbed, for at least a week.
	<ol>
		<li>Under a dissecting stereo microscope, orient the fly ventral side up.</li>
		<li>Using insect pins, pin the fly onto the plate by inserting one pin through the thorax and another pin through the most posterior end of the abdomen, near the genitalia (Figure 2A). It may be useful to cut the pins in half before pinning the specimen so as not to obstruct the dissection. Repeat with up to 10 flies per dissection plate. 
		NOTE: Optional: Remove the wings and legs before pinning fly to plate. This will help prevent a bubble forming around the fly when media is added.</li>
		<li>Once all flies have been pinned to the plate, add enough dissection media to cover the flies (~1 mL) using a transfer pipet.</li>
		<li>Using forceps or cuticle scissors, remove the head.</li>
		<li>Using cuticle scissors, make two horizontal incisions: one directly above the posterior pin in the abdomen, and another at the most anterior end of the abdomen, where the thorax and abdomen meet (Figure 2B, C). In Figure 2, the head was left intact to clarify orientation.</li>
		<li>Make a vertical incision, connecting the two horizontal incisions (the three cuts resemble the letter I). This will open up the abdominal cavity (Figure 2D).</li>
		<li>Using forceps, remove the internal organs and tissue, avoiding the dorsal vessel. If undisturbed, the transparent dorsal vessel can often be seen pulsating near the anterior end of the abdomen. Additional pins can be used to pin open newly cut ends of the cuticle (Figure 2E, F).</li>
		<li>Using cuticle scissors, remove the thorax. Alternatively, the thorax can be removed before mounting the dissected cuticles and dorsal vessel on a microscope slide.</li>
		<li>Repeat with remaining flies. &#160;dissect flies in a timely manner, to minimize possible variations in phagocytic rate. Once all flies have been dissected, leave the cuticles with the attached dorsal vessel pinned to the plate. All of step 5 will be carried out in the dissection plate. This will prevent damaging or accidentally discarding cuticles between steps.</li>
	</ol>
	</li>
</ol>
5. Fixation and staining
<ol>
	<li>Fix dissected cuticles with attached dorsal vessel in 4% paraformaldehyde (PFA).
	<ol>
		<li>Using a new disposable transfer pipet for each step, discard the dissection media, and replace with 1 mL of 4% PFA. Throughout the fixation and staining, keep the dissections protected from light as much as possible.</li>
		<li>Incubate at room temperature for 15 min with rocking at 20 rpm. Do not allow dissections to sit in fixative for more than 20 min, as this could start to damage the tissue.</li>
	</ol>
	</li>
	<li>Wash cuticles 2x in 1x PBS + 0.1% Tween (PBST).
	<ol>
		<li>Remove fixative and replace with 1 mL of 1x PBST.</li>
		<li>Wash at room temperature for 15 min with rocking.</li>
		<li>Repeat 1x. 
		NOTE: Dissected, fixed tissue can be stored at 4 &#176;C, for up to 3 days, protected from light, after the first wash by replacing the wash with fresh PBST. Do not store fixed tissue if antibodies will be used. Antibodies should be used with fresh tissue for best results.</li>
	</ol>
	</li>
	<li>Optional: Antibody staining. Antibodies can be used to clearly visualize the dorsal vessel clearly (Figure 3), or to detect hemocyte specific markers. This can ensure only cells along the dorsal vessel are counted or to mark the membrane of the hemocytes.
	<ol>
		<li>Remove the second wash, add primary antibody at the appropriate dilution. Incubate overnight at 4 &#176;C, with rocking.</li>
		<li>Remove primary antibody, and wash twice with PBST for 15 min with rocking.</li>
		<li>Add fluorescent secondary antibody. We recommend a green-fluorescent antibody so it does not obscure the fluorescent particles. Incubate at room temperature for 2 h, with rocking.</li>
		<li>Remove secondary antibody, wash twice for 15 min each with PBST.</li>
	</ol>
	</li>
	<li>Stain with DAPI.
	<ol>
		<li>Remove final wash and replace with 1 mL of DAPI diluted in PBST (1:1000).</li>
		<li>Stain for 20 min with rocking at room temperature.</li>
		<li>Remove DAPI, and wash 2x (repeat step 5.2).</li>
		<li>Replace final wash with fresh 1x PBST. 
		NOTE: Flies can be stored at 4 &#176;C, for up to 3 days, protected from light, after the first wash by replacing the wash with fresh PBST.</li>
	</ol>
	</li>
</ol>
6. Mounting cuticles onto microscope slides and imaging
<ol>
	<li>Prepare dissected cuticles.
	<ol>
		<li>Under the dissecting stereomicroscope, cut off excess cuticle that could interfere with imaging.</li>
		<li>Using forceps, transfer the cuticles with attached dorsal vessel into a 1.5 mL microcentrifuge tube containing 70% glycerol. Placing the cuticles in glycerol will help remove PBST and allows for a clearer image during imaging.</li>
	</ol>
	</li>
	<li>Mount cuticles onto the microscope slide.
	<ol>
		<li>Add a few drops of 70% glycerol to a microscope slide.</li>
		<li>Using forceps, remove cuticles from the glycerol tube and place in glycerol on the slide.</li>
		<li>Under the dissecting stereo microscope, use forceps to orient cuticles ventral side up, ensuring the dorsal vessel is visible. The darker pigment of the cuticle will be face down.</li>
		<li>Add an additional drop of glycerol, if needed. This helps prevent air bubbles and allows for a clearer image.</li>
		<li>Gently place a coverslip over cuticles and seal edges with fingernail polish. Allow to dry for 10-15 min before proceeding. Image the flies immediately or store in a lightproof box at 4 &#176;C.</li>
	</ol>
	</li>
	<li>Image the dorsal vessel.
	<ol>
		<li>Using a fluorescent microscope, use the structural interference system to generate optical sections of the dorsal vessel. A confocal microscope can alternatively be used which may provide additional accuracy. Obtain Z-stack images of the dorsal vessel using a 20x objective and preferred imaging software. Add a 10 mm scale bar, and properly label and save images as tiff files (Figure 4) or the desired format. 
		NOTE: The number of Z-stack images obtained can vary between dissections and depends on how well the dorsal vessel was dissected, and on the desired step size between images. Here, the step size was set to 0.49 mm. That number can range anywhere from 3 to 40 images per stack in our experience.</li>
	</ol>
	</li>
</ol>
7. Analyze images
<ol>
	<li>Quantify fluorescent events using ImageJ.
	<ol>
		<li>Open images and stack them: Image &#224; Stacks &#224; Images to Stack.</li>
		<li>Count only the ~1 mm sized fluorescent signals within a 10 mm diameter centered on a DAPI-positive nucleus by clicking on each event from at least 10 cells per fly, from at least 10 flies per age per particle type injected: Plugins &#224; Analyze &#224; Cell Counter Notice (Figure 5A). The cell counter notice tool assigns a different color to every cell tracked, with a colored dot that corresponds to every fluorescent event clicked on within that cell.</li>
		<li>To list the counter and stack position associated with each point, press &#8216;m&#8217; or select Measure under the Analyze tab, or to display the number of events counted in each cell in a results table, press &#8216;alt +y&#8217; (Figure 5B).</li>
		<li>Transfer the cell counts to a spreadsheet to be used for statistical analysis.</li>
	</ol>
	</li>
	<li>Perform statistical analysis.
	<ol>
		<li>Analyze differences in phagocytic events using either fixed-effects ANOVA or mixed-model nested ANOVA. Mixed models can be used to test the main fixed effects of age and genotype and the random effect of individuals nested within each genotype17. 
		NOTE: Investigators should be rigorous in testing the assumptions of any statistical procedure used to analyze the data.</li>
	</ol>
	</li>
</ol>

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R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Pericardin,+a+Drosophila+collagen,+facilitates+accumulation+of+hemocytes+at+the+heart.">Pericardin, a Drosophila collagen, facilitates accumulation of hemocytes at the heart.</a> Developmental Biology. 454 (1), 52-65 (2019).</li><li>Ghosh, S., Mandal, S., Mandal, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Detecting+proliferation+of+adult+hemocytes+in+Drosophila+by+BrdU+incorporation+and+PH3+expression+in+response+to+bacterial+infection.">Detecting proliferation of adult hemocytes in Drosophila by BrdU incorporation and PH3 expression in response to bacterial infection.</a> Wellcome Open Research. 3, (2018).</li><li>Hao, Y., Yu, S., Luo, F., Jin, L. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Jumu+is+required+for+circulating+hemocyte+differentiation+and+phagocytosis+in+Drosophila.">Jumu is required for circulating hemocyte differentiation and phagocytosis in Drosophila.</a> Cell Communication and Signaling. 16 (1), 95 (2018).</li><li>Petraki, S., Alexander, B., Br&#252;ckner, K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Assaying+blood+cell+populations+of+the+Drosophila+melanogaster+larva.">Assaying blood cell populations of the Drosophila melanogaster larva.</a> Journal of Visualized Experiments. (105), (2015).</li><li>Gyoergy, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tools+allowing+independent+visualization+and+genetic+manipulation+of+Drosophila+melanogaster+macrophages+and+surrounding+Tissues.">Tools allowing independent visualization and genetic manipulation of Drosophila melanogaster macrophages and surrounding Tissues.</a> G3: Genes, Genomes, Genetics. 8 (3), 845-857 (2018).</li><li>Bosch, P. S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Blood+cells+of+adult+Drosophila+do+not+expand,+but+control+survival+after+bacterial+infection+by+induction+of+Drosocin+around+their+reservoir+at+the+respiratory+epithelia.">Blood cells of adult Drosophila do not expand, but control survival after bacterial infection by induction of Drosocin around their reservoir at the respiratory epithelia.</a> BioRxiv. 578864, (2019).</li></ol>

The authors have nothing to disclose.

The protocol described here is a reliable way to quantify different aspects of phagocytosis, under controlled experimental conditions. We note that we have only tested this procedure with gram negative bacterial particles and results may differ if gram positive bacterial particles are used. Indeed, it would be interesting to compare the phagocytic responses to both gram negative and gram positive bacteria in different experimental conditions. The use of a nano-injector allows for precise control over injection volumes, ensuring each fly is injected with the same volume of particles. One limitation to the protocol comes from inconsistencies in particle preparations. Particles will aggregate once frozen, so small variations in dilution volumes, or lack of vortexing, can affect particle concentration between experiments. To minimize possible variations in particle concentrations between ages, it is beneficial to inject 1- and 5-week old flies on the same day, using the same needle and particle solution. Another potential drawback is that during dissections, the dorsal vessel and/or cuticle can easily be damaged if pins are not handled properly. To avoid disrupting the dorsal vessel, minimize the number of pins used per dissection. The advantage to this dissection method is that all fixation, washing and staining steps can be performed in the dissection plate. Because the cuticles are pinned down, this prevents the cuticles from being lost between steps.
Compared to existing methods18,19,25,26,27,28,29, the described protocol has its advantages and limitations. By dissecting the dorsal vessel, we are able to visualize and quantify individual hemocytes at this location. This makes it possible to detect subtle variations in phagocytic activity between experimental groups. Other methods visualize fluorescently labeled particles by collecting hemocytes using a Bleed/Scrape assay19,25,26,27, or through an intact ventral cuticle18,19,28,29; however, individual hemocytes cannot be assessed when visualized through the dorsal cuticle. The advantage of this protocol, when compared to the Bleed/Scrape method is that our method allows us to assess only those hemocytes associated with the dorsal vessel, and does account for circulating cells or those along the body wall, which may be functionally different. Dissecting the dorsal vessel also removes the need to include a second round of injections with a fluorescence quencher, like Trypan blue19,26. This is because any particles not bound to or engulfed by a cell will be washed away during wash steps. Conversely, alternative methods may be easier to perform because they do not require dissections. While dissecting the dorsal vessel is easy to learn, this step adds a level of complexity that may not be feasible in some experimental designs.
Although the described use of this in vivo phagocytosis assay is to assess and quantify phagocytic events between different ages, this protocol is highly adaptable and can be used to analyze different aspects of phagocytosis between genotype, sex, or tissue type. With phagocytosis being of central importance for most multicellular animals, understanding how this process declines with age could lead to better therapeutic treatments for the aging population. This approach offers long-term potential for elucidating aspects of age-related changes in the immune response, with special focus on phagocytosis.&#160;

The innate immune system, which consists of physical and chemical barriers to infection as well as cellular components, is evolutionary conserved across multicellular organisms1,2. As the first line of defense, the innate immune system plays a critical role in combating invading pathogens in all animals1,2,3. The components of the innate immune response include a wide range of cell types which are classified on the basis that they lack specificity and immunological memory2,3,4. In humans, these cell types include phagocytic monocytes and macrophages, neutrophils, and cytotoxic natural killer cells4,5. While having a functional immune system is imperative for host survival, it is clear that the function of immune cells declines with age, a phenomenon known as immunosenescence5,6. Being able to assess age related changes in the immune response, including different aspects of the process of phagocytosis, could aid in our understanding of immunosenescence. The procedure we describe here provides an effective and repeatable approach to evaluate and quantify phagocytic events by hemocytes in Drosophila melanogaster. 
Drosophila is an ideal model for studying the immune response for many reasons. For one, there is an extensive set of genetic tools available that make it possible to easily manipulate gene expression in a tissue-dependent manner7. These tools include a collection of mutants, RNA interference stocks, GAL4/UAS stocks, and the Drosophila Genetic Reference Panel that contains 205 different inbred lines for which the entire genome sequences are catalogued8. The short life cycle of Drosophila and the large number of individuals produced allow researchers to test multiple individuals in a controlled environment, in a short period of time. This greatly improves the ability to identify subtle differences in immune responses to infection among genotypes, between sexes or across ages. Importantly, many genetic components and functions of the innate immune response, including phagocytosis, are evolutionarily conserved between Drosophila and mammals1,2.
In Drosophila, the process of phagocytosis that follows infection is carried out by phagocytic hemocytes called plasmatocytes, which are equivalent to mammalian macrophages9. Hemocytes are essential for recognizing a wide range of particles and clearing microbial pathogens9,10,11,12,13. These cells express a variety of receptors that must differentiate self from non-self, and initiate signaling events needed to carry out the phagocytic process10,11,12,13,14,15. Once a particle is bound, it starts to be internalized by reorganization of the actin cytoskeleton and remodeling of the plasma membrane to expand around the particle, forming a phagocytic cup11,12,13,14. During this process, another set of signals tells the cell to internalize the particle further by closing the phagocytic cup, forming a membrane-bound phagosome11,12,13,14,15. The phagosome then undergoes a maturation process, associating with different proteins and fusing with lysosomes, forming an acidic phagolysosome11,12,13,14,15. At this point, particles can efficiently be degraded and eliminated11,12,13,14,15. Drosophila studies have revealed that older flies (4 weeks of age) have a reduced ability to clear an infection compared to younger flies (1-week old), likely due, at least in part, to a decline in some aspects of phagocytosis16,17.
The method described here utilizes two separate fluorescently-labelled heat-killed E. coli particles, one bearing a standard fluorophore and one that is pH sensitive, to assess two different aspects of phagocytosis: the initial engulfment of particles, and the degradation of particles in the phagolysosome. In this assay, fluoro-particle fluorescence is observable when the particles are bound and engulfed by hemocytes, while pH sensitive particles fluoresce only in the low pH conditions of the phagosome. Fluorescent events can then be observed in hemocytes that localize along the dorsal vessel. We focus on hemocytes localized to the dorsal vessel, which provide an anatomical landmark to locate hemocytes that are known to contribute to bacterial clearance, and to consistently isolate them. However, hemocytes in other parts of the body and the hemolymph are also important for clearance. Although we have not studied this cell population, our general procedure could be applicable for phagocytic assays of these cells as well. One advantage of our approach is that we can quantify phagocytic events within individual hemocytes, allowing us to detect subtle variation in phagocytic processes. Other studies that visualize fluorescent events through the cuticle18,19 do not account for differences in the numbers of hemocytes present, which is especially important to consider in our case as total hemocyte counts are expected to change with age17.

<table><tbody><tr><td>0.10 mm Insect pins</td><td>Fine Science Tools</td><td>26002-10</td><td>Here: pins are cut in half, and the sharp end is used</td></tr><tr><td>1 mL sterile syringes</td><td>Becton Dickinson</td><td>309602</td><td>Filled with mineral oil to load needle</td></tr><tr><td>15% Fetal Bovine Serum (FBS)</td><td>Gibco</td><td>16000-044</td><td>for dissection media</td></tr><tr><td>16 % Paraformaldehyde</td><td>Electron Microscopy Sciences</td><td>15710</td><td>EM-grade, 4% working, diluted in 1X PBS</td></tr><tr><td>1x Phosphate buffered saline (PBS)</td><td>Sigma</td><td>P3813</td><td></td></tr><tr><td>3 mL Trasnfer Pipet</td><td>Falcon</td><td>357524</td><td></td></tr><tr><td>3.5&quot; Glass Capillaries</td><td>Drummond</td><td>3-000-203-G/X</td><td>1.14mm O.D X 3.5&quot; length X 0.53&quot; I.D</td></tr><tr><td>35x10 mm Petri dishes</td><td>Becton Dickinson</td><td>351008</td><td>Used as dissection plate, filled half way with Sylgard</td></tr><tr><td>6x penicillin/streptomycin</td><td>Life Technologies</td><td>15140-122</td><td>for dissection media</td></tr><tr><td>70% Glycerol</td><td>Sigma</td><td>G9012</td><td></td></tr><tr><td>Analog Vortex mixer</td><td>VWR</td><td>58816-121</td><td></td></tr><tr><td>Biological point forceps, Dumont No. 5</td><td>Fine Science Tools</td><td>11295-10</td><td></td></tr><tr><td>DAPI (4&#039;,6-diamidino-2-phenylindole)</td><td>Life Technologies</td><td>D1306</td><td>Diluted 1:1000 in 1x PBST</td></tr><tr><td>Drosophila strain</td><td></td><td></td><td>w[*]; P{w[+mC]=He-GAL4.Z}85, P{w[+mC]=UAS-GFP.nls}8</td></tr><tr><td>E. coli (K-12 strain) BioParticles&amp;trade;, Alexa Fluor&amp;trade; 594 conjugate</td><td>Life Technologies</td><td>E23370</td><td></td></tr><tr><td>Glass slides</td><td>Premiere</td><td>D17026102</td><td></td></tr><tr><td>Live cell imaging solution</td><td>Life Technologies</td><td>A14291DJ</td><td>preferred buffer for particle preparation and dilutions</td></tr><tr><td>Mineral oil</td><td>Mpbio</td><td>194836</td><td></td></tr><tr><td>Nanoject II automatic nanoliter injector</td><td>Drummond</td><td>3-000-204</td><td></td></tr><tr><td>Narrow Polystyrene Super Bulk Drosophila Vials</td><td>Genesee</td><td>32-116SB</td><td>Size: 25 X 95 mm</td></tr><tr><td>Nutating Mixer</td><td>Fisher Scientific</td><td>88-861-043</td><td>Speed used: 20 rpm</td></tr><tr><td>pHrodo&amp;trade; Red E. coli BioParticles&amp;trade; Conjugate for Phagocytosis</td><td>Life Technologies</td><td>P35361</td><td></td></tr><tr><td>Schneider&#039;s Drosophila cell culture media (1x)</td><td>Gibco</td><td>21720-024</td><td>Dissection media, combine: Schneiders, FBS, and pen/strep; filter sterilize</td></tr><tr><td>Sodium azide</td><td>Sigma-Aldrich</td><td>S2002</td><td>2mM (or 20%) working</td></tr><tr><td>Spring scissors</td><td>Fine Science Tools</td><td>15000-00</td><td></td></tr><tr><td>Sylgard 184 Silicone elastomer</td><td>Electron Microscopy Sciences</td><td>24236-10</td><td>Prepare according to provided protocol</td></tr><tr><td>Tween 20</td><td>Sigma</td><td>P1379</td><td>For PBS + 0.1% tween</td></tr><tr><td>Vertical Pipette Puller Model 700C</td><td>David Kopf Instruments</td><td>812368</td><td>Heater: 55? Solenoid: 45</td></tr><tr><td>Zeiss AxioImager.Z1 fluorescent microscope</td><td>Zeiss</td><td></td><td>Here: Apotome structural interference system with Zeiss Zen imaging software</td></tr></tbody></table>

assessing the age-specific phagocytic ability of adult drosophila melanogaster hemocytes using an in vivo phagocytosis assay

Phagocytosis is an essential function of the innate immune response. This process is carried out by phagocytic hemocytes whose primary function is to recognize a wide range of particles and destroy microbial pathogens. As organisms age, this process begins to decline, yet little is known about the underlying mechanisms or the genetic basis of immunosenescence. Here, an injection based in vivo phagocytosis assay is used to assess age related changes in different aspects of phagocytosis, such as binding, engulfment, and degradation of internalized particles, by quantifying phagocytic events in hemocytes in adult Drosophila. Drosophila melanogaster has become an ideal model to investigate age related changes in innate immune function for many reasons. For one, many genetic components and functions of the innate immune response, including phagocytosis, are evolutionarily conserved between Drosophila and mammals. Because of that, results obtained from using this protocol are likely to be widely relevant to understanding the age related changes in immune function in a variety of organisms. Additionally, we note that this method provides quantitative estimates of hemocyte phagocytic ability, which could be useful for a variety of research topics, and need not be limited to studies of aging.

To illustrate the described injection methods, Figure 1A shows the injection site on Drosophila melanogaster, as well as how food dye allows for a visual confirmation that the fly was injected (Figure 1B). The addition of food dye also aids in the recognition of a clogged needle. Injections can be performed in the abdomen, but keep the injection site consistent across experiments. This will help minimize possible variations between each experiment.
To visualize the fluorescently labeled particles within resident hemocytes along the dorsal vessel, we dissected the dorsal vessel and attached abdominal cuticle. Figure 2A-F outlines the dissection methods.
To assess the age-specific ability of young and aged flies to carry out phagocytosis, hemocytes along the dorsal vessel are visualized using a fluorescent microscope. To ensure that only cells along the dorsal vessel are counted, antibodies or GFP-tagged genes for certain blood cell markers or heart specific collagen, such as Hemese and Hemolectin, or Pericardin (Figure 3), respectively, can be used22,23,24. Fluorescently labeled E. coli particles are 1 mm in length, while hemocytes are 10 mm in diameter17. Only those fluorescent events located within a 10 mm diameter centered on a DAPI-positive nucleus are counted (Figure 4). To quantify fluorescent events, ImageJ software is used (Figure 5).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/60983/60983fig1.jpg" /> 
Figure 1: Injection site and visual verification. (A) Lateral side of thorax is pierced with a pulled-capillary needle. (B) Injections are visually verified by adding green food dye to particle solution. <a href="https://www.jove.com/files/ftp_upload/60983/60983fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/60983/60983fig2.jpg" /> 
Figure 2: Dorsal vessel dissection. (A) Pins are placed in the thorax and posterior abdomen (black arrows). (B-C) Two horizontal incisions (green arrows) are made at the posterior end of the abdomen (B), and anterior end (C). (D) A vertical incision (green arrow) is made down the middle of the abdomen, connecting the two horizontal cuts. (E) Optional pins (*) are used to filet open the abdominal cavity, exposing internal tissue. (F) Internal tissue (crop, gut, uterus, ovaries, fat bodies) is removed, exposing the dorsal vessel. <a href="https://www.jove.com/files/ftp_upload/60983/60983fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/60983/60983fig3.jpg" /> 
Figure 3: Ventral view of a dissected dorsal vessel from a 5-week old female injected with pH sensitive particles, stained with antibody directed against Pericardin (A). Dotted white line outlines the lateral side of the dorsal vessel, with arrow pointing towards the anterior region. (B) Enlarged image of (A): clusters of hemocytes (blue arrow) that were actively degrading bacteria, within the first aortic chamber of the dorsal vessel. (C) Enlarged image of (A) outlining the extracellular matrix (ECM) collagen-like protein, Pericardin (green arrow), that holds the dorsal vessel in place24. <a href="https://www.jove.com/files/ftp_upload/60983/60983fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/60983/60983fig4.jpg" /> 
Figure 4: Dissected dorsal vessel and associated hemocytes from a female fly injected with pH sensitive particles, or fluoro-particles. (A) The dorsal vessel and associated hemocytes with engulfed pH sensitive-labelled E. coli particles (red), or (E) fluoro-labelled E. coli particles (red), isolated from a 1-week old fly, after recovering for 60 min. (B,F) Magnified inset of (A) and (E) (white box), respectively, showing two individual hemocytes with countable events. (C) The dorsal vessel and associated hemocytes with engulfed pH sensitive-labelled E. coli particles(red), or ( G) fluoro-labelled E. coli particles (red), isolated from a 5-week old fly, after recovering for 60 min. (D,H) Magnified inset of (C) and (G) (white box), respectively, showing two individual hemocytes with countable events. Dotted white line outlines the lateral side of the dorsal vessel, with arrow pointing towards the anterior region. Nuclei stained with DAPI (blue). <a href="https://www.jove.com/files/ftp_upload/60983/60983fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/60983/60983fig5.jpg" /> 
Figure 5: Quantifying phagocytic events within a 10 mm hemocytes using the cell counter in ImageJ. (A) After opening image(s) in ImageJ, the Cell Counter Notice tool can be used to keep track of phagocytic events per cell. (B) This tool will assign a different color to each cell selected to be counted, with each dot corresponding to a fluorescent event within that cell. Pressing &#8216;alt+y&#8217; will display a table showing the number of events counted per cell. <a href="https://www.jove.com/files/ftp_upload/60983/60983fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Assessing the Age-Specific Phagocytic Ability of Adult Drosophila melanogaster Hemocytes using an In Vivo Phagocytosis Assay at JoVE.com

Assessing the Age-Specific Phagocytic Ability of Adult Drosophila melanogaster Hemocytes using an In Vivo Phagocytosis Assay

This protocol describes an in vivo assay of phagocytosis used to assess and quantify the ability of young and aged Drosophila melanogaster hemocytes to phagocytose bacteria.

Assessing the Age-Specific Phagocytic Ability of Adult Drosophila melanogaster Hemocytes using an In Vivo Phagocytosis Assay

Phagocytosis is an essential function of the innate immune response. This process is carried out by phagocytic hemocytes whose primary function is to ...

assessing-age-specific-phagocytic-ability-adult-drosophila

Research

JoVE Journal

Biology

6.7K Views.  University of Maryland Baltimore County. Ons protocol biedt een effectieve en herhaalbare aanpak om fagocytische voorvallen in hemocyten te evalueren en te kwantificeren. Het belangrijkste voordeel van deze techniek is dat we fagocytische gebeurtenissen binnen individuele hemocyten kunnen kwantificeren, waardoor we variaties in fagocytische processen tussen genotypes bij individuele vliegen kunnen detecteren. Het uitvoeren van dissecties kan een uitdaging zijn, dus bij het uitvoeren van deze techniek voor de eerste keer, oefen disse...

Video: Assessing the Age-Specific Phagocytic Ability of Adult Drosophila melanogaster Hemocytes using an In Vivo Phagocytosis Assay

Dissection of Larval CNS in Drosophila Melanogaster

The central nervous system (CNS) of Drosophila larvae is complex and poorly understood.  One way to investigate the CNS is to use immunohistochemistry to examine the expression of various novel and marker proteins.  Staining of whole larvae is impractical because the tough cuticle prevents antibodies from penetrating inside the body cavity.  In order to stain these tissues it is necessary to dissect the animal prior to fixing and staining.  In this article we demonstrate how to dissect Drosophila larvae without damaging the CNS.  Begin by tearing the larva in half with a pair of fine forceps, and then turn the cuticle "inside-out" to expose the CNS.  If the dissection is performed carefully the CNS will remain attached to the cuticle.  We usually keep the CNS attached to the cuticle throughout the fixation and staining steps, and only completely remove the CNS from the cuticle just prior to mounting the samples on glass slides.  We also show some representative images of a larval CNS stained with Eve, a transcription factor expressed in a subset of neurons in the CNS.  The article concludes with a discussion of some of the practical uses of this technique and the potential difficulties that may arise.

In this article we demonstrate how to dissect the central nervous system from third instar Drosophila larvae.

The central nervous system (CNS) of Drosophila larvae is complex and poorly understood.  One way to investigate the CNS is to use immunohistochemistry to ...

Assaying Blood Cell Populations of the Drosophila melanogaster Larva

In vertebrates, hematopoiesis is regulated by inductive microenvironments (niches). Likewise, in the invertebrate model organism&#160;Drosophila melanogaster, inductive microenvironments known as larval Hematopoietic Pockets (HPs) have been identified as anatomical sites for the development and regulation of blood cells (hemocytes), in particular of the self-renewing macrophage lineage.&#160;HPs are segmentally repeated pockets between the epidermis and muscle layers of the larva, which also comprise sensory neurons of the peripheral nervous system. In the larva, resident (sessile) hemocytes are exposed to anti-apoptotic, adhesive and proliferative cues from these sensory neurons and potentially other components of the HPs, such as the lining muscle and epithelial layers. During normal development, gradual release of resident hemocytes from the HPs fuels the population of circulating hemocytes, which culminates in the release of most of the resident hemocytes at the beginning of metamorphosis. Immune assaults, physical injury or mechanical disturbance trigger the premature release of resident hemocytes into circulation. The switch of larval hemocytes between resident locations and circulation raises the need for a common standard/procedure to selectively isolate and quantify these two populations of blood cells from single Drosophila larvae. Accordingly, this protocol describes an automated method to release and quantify the resident and circulating hemocytes from single larvae. The method facilitates ex vivo approaches, and may be adapted to serve a variety of developmental stages of Drosophila and other invertebrate organisms.

Assaying Blood Cell Populations of the Drosophila melanogaster Larva

Drosophila blood cells, or hemocytes, cycle between resident sites and circulation. In the larva, resident (sessile) hemocytes localize to inductive microenvironments, the Hematopoietic Pockets, while circulating hemocytes move freely in the hemolymph. The goal of this protocol is the standardized isolation and quantification of these two, behaviorally distinct but interchanging, hemocyte populations.

In vertebrates, hematopoiesis is regulated by inductive microenvironments (niches). Likewise, in the invertebrate model organism&#160;Drosophila ...

Developmental Biology

Methods to Examine the Lymph Gland and Hemocytes in Drosophila Larvae

Many parallels exist between the Drosophila and mammalian hematopoietic systems, even though Drosophila lack the lymphoid lineage that characterize mammalian adaptive immunity. Drosophila and mammalian hematopoiesis occur in spatially and temporally distinct phases to produce several blood cell lineages. Both systems maintain reservoirs of blood cell progenitors with which to expand or replace mature lineages. The hematopoietic system allows Drosophila and mammals to respond to and to adapt to immune challenges. Importantly, the transcriptional regulators and signaling pathways that control the generation, maintenance, and function of the hematopoietic system are conserved from flies to mammals. These similarities allow Drosophila to be used to genetically model hematopoietic development and disease.
Here we detail assays to examine the hematopoietic system of Drosophila larvae. In particular, we outline methods to measure blood cell numbers and concentration, visualize a specific mature lineage in vivo, and perform immunohistochemistry on blood cells in circulation and in the hematopoietic organ. These assays can reveal changes in gene expression and cellular processes including signaling, survival, proliferation, and differentiation and can be used to investigate a variety of questions concerning hematopoiesis. Combined with the genetic tools available in Drosophila, these assays can be used to evaluate the hematopoietic system upon defined genetic alterations. While not specifically outlined here, these assays can also be used to examine the effect of environmental alterations, such as infection or diet, on the hematopoietic system.

Methods to Examine the Lymph Gland and Hemocytes in Drosophila Larvae

Drosophila and mammalian hematopoietic systems share many common features, making Drosophila an attractive genetic model to study hematopoiesis. Here we demonstrate dissection and mounting of the major larval hematopoietic organ for immunohistochemistry. We also describe methods to assay various larval hematopoietic compartments including circulating hemocytes and sessile crystal cells.

Many parallels exist between the Drosophila and mammalian hematopoietic systems, even though Drosophila lack the lymphoid lineage that characterize ...

High-Resolution Video Tracking of Locomotion in Adult Drosophila Melanogaster

Flies provide an important model for studying complex behavior due to the plethora of genetic tools available to researchers in this field. Studying locomotor behavior in Drosophila melanogaster relies on the ability to be able to quantify changes in motion during or in response to a given task. For this reason, a high-resolution video tracking system, such as the one we describe in this paper, is a valuable tool for measuring locomotion in real-time. Our protocol involves the use of an initial air pulse to break the flies momentum, followed by a thirty second filming period in a square chamber. A tracking program is then used to calculate the instantaneous speed of each fly within the chamber in 10 msec increments. Analysis software then compiles this data, and outputs a variety of parameters such as average speed, max speed, time spent in motion, acceleration, etc. This protocol will discuss proper feeding and management of flies for behavioral tasks, handling flies without anesthetization or immobilization, setting up a controlled environment, and running the assay from start to finish.

The study of complex locomotor behavior in Drosophila melanogaster is dependent upon the ability to quantify changes in a given fly's movement. This article demonstrates how to do this using a high-resolution tracking system.

Flies provide an important model for studying complex behavior due to the plethora of genetic tools available to researchers in this field.  Studying ...

Dissection of Oenocytes from Adult Drosophila melanogaster

In Drosophila melanogaster, as in other insects, a waxy layer on the outer surface of the cuticle, composed primarily of hydrocarbon compounds, provides protection against desiccation and other environmental challenges. Several of these cuticular hydrocarbon (CHC) compounds also function as semiochemical signals, and as such mediate pheromonal communications between members of the same species, or in some instances between different species, and influence behavior. Specialized cells referred to as oenocytes are regarded as the primary site for CHC synthesis. However, relatively little is known regarding the involvement of the oenocytes in the regulation of the biosynthetic, transport, and deposition pathways contributing to CHC output. Given the significant role that CHCs play in several aspects of insect biology, including chemical communication, desiccation resistance, and immunity, it is important to gain a greater understanding of the molecular and genetic regulation of CHC production within these specialized cells. The adult oenocytes of D. melanogaster are located within the abdominal integument, and are metamerically arrayed in ribbon-like clusters radiating along the inner cuticular surface of each abdominal segment. In this video article we demonstrate a dissection technique used for the preparation of oenocytes from adult D. melanogaster. Specifically, we provide a detailed step-by-step demonstration of (1) how to fillet prepare an adult Drosophila abdomen, (2) how to identify the oenocytes and discern them from other tissues, and (3) how to remove intact oenocyte clusters from the abdominal integument. A brief experimental illustration of how this preparation can be used to examine the expression of genes involved in hydrocarbon synthesis is included. The dissected preparation demonstrated herein will allow for the detailed molecular and genetic analysis of oenocyte function in the adult fruit fly.

Dissection of Oenocytes from Adult Drosophila melanogaster

In insects, the oenocytes produce cuticular hydrocarbon compounds. These compounds protect against desiccation and facilitate chemical communication. Here we demonstrate a dissection technique used to isolate the oenocytes from adult Drosophila melanogaster, and illustrate how this preparation can be utilized to study genes involved in hydrocarbon synthesis.

In Drosophila melanogaster, as in other insects, a waxy layer on the outer surface of the cuticle, composed primarily of hydrocarbon compounds, provides ...

Phagocytosis Assay for Apoptotic Cells in Drosophila Embryos

The molecular mechanisms underlying the phagocytosis of apoptotic cells need to be elucidated in more detail because of its role in immune and inflammatory intractable diseases. We herein developed an experimental method to investigate phagocytosis quantitatively using the fruit fly Drosophila, in which the gene network controlling engulfment reactions is evolutionally conserved from mammals. In order to accurately detect and count engulfing and un-engulfing phagocytes using whole animals, Drosophila embryos were homogenized to obtain dispersed cells including phagocytes and apoptotic cells. The use of dispersed embryonic cells enables us to measure in vivo phagocytosis levels as if we performed an in vitro phagocytosis assay in which it is possible to observe all phagocytes and apoptotic cells in whole embryos and precisely quantify the level of phagocytosis. We confirmed that this method reproduces those of previous studies that identified the genes required for the phagocytosis of apoptotic cells. This method allows the engulfment of dead cells to be analyzed, and when combined with the powerful genetics of Drosophila, will reveal the complex phagocytic reactions comprised of the migration, recognition, engulfment, and degradation of apoptotic cells by phagocytes.

Phagocytosis Assay for Apoptotic Cells in Drosophila Embryos

We herein describe a phagocytosis assay using the dispersed embryonic cells of Drosophila. It enables us to easily and precisely quantify in vivo phagocytosis levels, and to identify new molecules required for the phagocytosis of apoptotic cells.

The molecular mechanisms underlying the phagocytosis of apoptotic cells need to be elucidated in more detail because of its role in immune and ...

Immunology and Infection

Extraction of Hemocytes from Drosophila melanogaster Larvae for Microbial Infection and Analysis

During the pathogenic infection of Drosophila melanogaster, hemocytes play an important role in the immune response throughout the infection. Thus, the goal of this protocol is to develop a method to visualize the pathogen invasion in a specific immune compartment of flies, namely hemocytes. Using the method presented here, up to 3 &#215; 106 live hemocytes can be obtained from 200 Drosophila 3rd instar larvae in 30 min for ex vivo infection. Alternatively, hemocytes can be infected in vivo through injection of 3rd instar larvae followed by hemocyte extraction up to 24 h post-infection. These infected primary cells were fixed, stained, and imaged using confocal microscopy. Then, 3D representations were generated from the images to definitively show pathogen invasion. Additionally, high-quality RNA for qRT-PCR can be obtained for the detection of pathogen mRNA following infection, and sufficient protein can be extracted from these cells for Western blot analysis. Taken together, we present a method for definite reconciliation of pathogen invasion and confirmation of infection using bacterial and viral pathogen types and an efficient method for hemocyte extraction to obtain enough live hemocytes from Drosophila larvae for ex vivo and in vivo infection experiments.

Extraction of Hemocytes from Drosophila melanogaster Larvae for Microbial Infection and Analysis

This method demonstrates how to visualize pathogen invasion into insect cells with three-dimensional (3D) models. Hemocytes from Drosophila larvae were infected with viral or bacterial pathogens, either ex vivo or in vivo. Infected hemocytes were then fixed and stained for imaging with a confocal microscope and subsequent 3D cellular reconstruction.

During the pathogenic infection of Drosophila melanogaster, hemocytes play an important role in the immune response throughout the infection. Thus, the ...

Assessing the Cellular Immune Response of the Fruit Fly, Drosophila melanogaster, Using an In Vivo Phagocytosis Assay

In all animals, innate immunity provides an immediate and robust defense against a broad spectrum of pathogens. Humoral and cellular immune responses are the main branches of innate immunity, and many of the factors regulating these responses are evolutionarily conserved between invertebrates and mammals. Phagocytosis, the central component of cellular innate immunity, is carried out by specialized blood cells of the immune system. The fruit fly, Drosophila melanogaster, has emerged as a powerful genetic model to investigate the molecular mechanisms and physiological impacts of phagocytosis in whole animals. Here we demonstrate an injection-based in vivo phagocytosis assay to quantify the particle uptake and destruction by Drosophila blood cells, hemocytes. The procedure allows researchers to precisely control the particle concentration and dose, making it possible to obtain highly reproducible results in a short amount of time. The experiment is quantitative, easy to perform, and can be applied to screen for host factors that influence pathogen recognition, uptake, and clearance.

Assessing the Cellular Immune Response of the Fruit Fly, Drosophila melanogaster, Using an In Vivo Phagocytosis Assay

This protocol describes an in vivo phagocytosis assay in adult Drosophila melanogaster to quantify phagocyte recognition and clearance of microbial infections.

In all animals, innate immunity provides an immediate and robust defense against a broad spectrum of pathogens. Humoral and cellular immune responses are ...

Cuticle Disruption: A Method to Collect Hemolymph from Drosophila Larvae

Source: Reimels, T. A. and Pfleger, C. M. <a href="https://www.jove.com/video/54544/" target="_blank">Methods to Examine the Lymph Gland and Hemocytes in Drosophila Larvae</a>. J. Vis. Exp. (2016).
The Drosophila hemolymph serves as both blood and interstitial fluid, circulating throughout the body during the larva and adult stages. This video describes a protocol to collect larval hemolymph in order to quantify the circulating cells.

Source: Reimels, T. A. and Pfleger, C. M. Methods to Examine the Lymph Gland and Hemocytes in Drosophila Larvae. J. Vis. Exp. (2016).
The Drosophila ...

JoVE Encyclopedia of Experiments

Drosophila melanogaster (fruit fly)

Larva

An In Vivo Assay to Quantify Bacterial Phagocytosis in Adult Drosophila Flies

Source: Nazario-Toole, A. E., et al. <a href="https://app.jove.com/v/59543">Assessing the Cellular Immune Response of the Fruit Fly, Drosophila melanogaster, Using an In Vivo Phagocytosis Assay.</a> J. Vis. Exp. (2019)
This video demonstrates an in vivo assay designed to measure bacterial phagocytosis in adult Drosophila flies. Following the injection of fluorescently labeled bacteria into the abdomen of adult flies, hemocytes associated with the dorsal vessel engage in phagocytosis. The introduction of trypan blue dye serves to quench the fluorescence emitted by extracellular, non-phagocytosed bacteria. This quenching process enhances the identification of phagocytosed bacteria when observed under a fluorescence microscope.

1. Prepare Fluorescein particles for injection

	Reconstitute 10 mg of commercially available, heat-killed bacteria particles labeled with fluorescein ...

Assessing the Age-Specific Phagocytic Ability of Adult Drosophila melanogaster Hemocytes using an In Vivo Phagocytosis Assay

Samenvatting

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