In Vivo Imaging of Dauer-specific Neuronal Remodeling in C. elegans

Summary

Following exposure to specific environmental stressors, the nematode Caenorhabditis elegans undergoes extensive phenotypic plasticity to enter into a stress-resistant ‘dauer’ juvenile stage. We present methods for the controlled induction and imaging of neuroplasticity during dauer.

Abstract

The mechanisms controlling stress-induced phenotypic plasticity in animals are frequently complex and difficult to study in vivo. A classic example of stress-induced plasticity is the dauer stage of C. elegans. Dauers are an alternative developmental larval stage formed under conditions of low concentrations of bacterial food and high concentrations of a dauer pheromone. Dauers display extensive developmental and behavioral plasticity. For example, a set of four inner-labial quadrant (IL2Q) neurons undergo extensive reversible remodeling during dauer formation. Utilizing the well-known environmental pathways regulating dauer entry, a previously established method for the production of crude dauer pheromone from large-scale liquid nematode cultures is demonstrated. With this method, a concentration of 50,000 - 75,000 nematodes/ml of liquid culture is sufficient to produce a highly potent crude dauer pheromone. The crude pheromone potency is determined by a dose-response bioassay. Finally, the methods used for in vivo time-lapse imaging of the IL2Qs during dauer formation are described.

Introduction

Phenotypic plasticity, including developmental and behavioral plasticity, is important for adaptations to adverse environmental conditions and is considered a driving force in evolution¹. C. elegans is a model organism frequently used for studies in development and neurobiology. Under ideal conditions, C. elegans develops through four larval stages prior to entering the adult reproductive stage. However, under conditions of low food availability and high population densities, C. elegans can undergo a developmental switch and enter into a long-lived and stress-resistant dauer stage². Dauers display several morphological and behavioral differences from non-dauers which likely mediate this stress resistance. The environmental cues and genetic pathways regulating dauer entry have been extensively described^{3, 4, 5, 6, 7}. However, the molecular mechanisms controlling individual phenotypic changes that occur during dauer formation are less well understood.

The examination of dauer-specific phenotypes requires the production of dauer animals. This can be accomplished in three ways: 1) Picking from a starved culture of C. elegans, 2) Use of dauer formation constitutive (daf-c) mutants, 3) Induction of dauer formation through purified pheromone. It is relatively simple to pick dauers from a standard NGM plate with a C. elegans population that has exhausted its bacterial food-supply. In our hands, a standard NGM plate originally seeded with 50 µl of OP50 Escherichia coli, allowed to grow for 3 days and subsequently inoculated with 3 - 4 adult hermaphrodites kept at 25 °C will exhaust the food supply within one week and produce several thousand dauers within an additional 3 days (in addition to numerous starved non-dauers). However, this method is unsatisfactory for examining processes occurring during the molt into dauer. It is difficult to determine which of the several thousand animals on a typical starved plate are entering into dauer. Furthermore, use of a starved plate offers no possibility for synchronization. The use of daf-c mutants allows for synchronization and the reliable generation of dauers. However, there is no guarantee that a particular daf-c mutation will not affect other dauer-specific phenotypes alone or in combination with additional mutations.

The presence of a dauer pheromone was first implied by Cassada and Russell and later demonstrated by Golden and Riddle. The dauer pheromone has since been chemically characterized^{2, 8, 9, 10}. The purified pheromone consists of a complex blend of ascarosides, which in different forms regulate both behavioral and developmental processes^{9, 11}. Use of a crude dauer pheromone extract allows for reliable controlled induction of synchronized dauers in a wild-type background.

The nervous system and associated glial cells undergo remodeling during dauer larva formation^{12, 13, 14}. Some of these changes are irreversible, such as the remodeling of glia cells during dauer^{13, 14}. However other remodeling events are reversible upon a return to favorable environmental conditions. For example, a set of four IL2Q neurons undergo rapid and reversible neuronal remodeling during dauer formation including: dendrite arborization, a switch from single dendritic to multidendritic neurons and axon remodeling¹². The methods herein allow for the reliable in vivo imaging of stress-induced neuroplasticity in a model organism. The methods presented for the production and testing of crude dauer pheromone are previously described and compiled from several sources^{4, 8, 15, 16, 17, 18}.

Protocol

1. Crude Dauer Pheromone Production

1. Grow OP50 E. coli from a single colony O/N at 37 °C while shaking in 100 ml of LB broth at 200 rpm. NOTE: This O/N culture can be made in advance and stored at 4 °C.
2. Grow N2 C. elegans on 15 - 20 6 cm Petri dishes with NGM agar (See recipe in Table 1) seeded with 50 µl of OP50 E. coli until the bacteria is almost depleted¹⁹.
3. Make 5x 250 ml of S media (See recipe in Table 1) in 1 L Erlenmeyer flasks¹⁹. NOTE: This solution can be made in advance.
4. Grow a culture of OP50 E. coli in 4 L of LB broth O/N by inoculating with 1 ml of OP50 in E. coli and shaking at 37 °C for 16 hr.
5. Wash the nematodes from plates (step 1.2) with 1 ml of S basal solution (See recipe in Table 1) and transfer nematodes from 4-5 plates into each of 4 1 L Erlenmeyer flasks with the S media prepared in Step 1.3 (4-5 plates for each flask)¹⁹.
6. Centrifuge the OP50 from step 1.4 at 650 x g for 10 min and remove supernatant. Resuspend each bacterial pellet in 10 ml of S basal solution. Transfer equal amounts of resuspended bacteria to each flask of nematodes.
7. Place the flasks on an orbital shaker at room temperature (20 - 25 °C) and 100 - 150 rpm for 4 - 5 days until the solution begins to clear, indicating a depletion of food.
8. Once the food is depleted, grow another O/N culture of OP50 E. coli in 4x 1 L of LB broth. Centrifuge the bacteria at 650 x g for 10 min and add a pellet from one flask to each of the S media flasks with nematodes. Return the S media flasks to the orbital shaker, as in step 1.7, for an additional 3-4 days until the food is depleted again.
9. Take a ~1 ml aliquot of solution from each flask and estimate the nematode concentration by sub-sampling 1 µl from each 1 ml aliquot and counting the number of nematodes. NOTE: The nematode population should be 50,000 - 75,000 nematodes/ml. At this concentration the majority of nematodes are dauers.
10. Discard any contaminated flasks. NOTE: Contamination frequently manifests as fungal hyphae seen during step 1.9.
11. Centrifuge nematodes at 4,000 x g for 10 min at 4 °C. Discard the nematode pellet and retain the supernatant. Alternatively, see the discussion for using these animals to make a low-potency pheromone.
12. Filter the supernatant through #1 Whatman filter paper. NOTE: A vacuum flask will expedite this process.
13. Further filter the supernatant through 0.45 µm sterile vacuum filtration units. NOTE: Filtrate can be kept O/N at 4 °C or proceed to 1.14.
14. Add the filtrate to a 2 L beaker with a stir bar. Place in a fume hood on a heating stir plate. Bring to a boil while stirring and evaporate to approximately 200 ml. Transfer the solution to a 500 ml beaker. Continue boiling until approximately 50 ml are left. NOTE: Care should be taken during this step as it is possible for the solution to boil over. The color of the final 50 ml is a dark brown. At any time during the cooking process, the heat can be turned off and the filtrate stored O/N at RT or 4 °C.
15. Let cool and centrifuge for 5 min at 1,000 x g. Pour the supernatant into a 100 ml beaker and discard the pellet.
16. Boil the supernatant down to a brown crust. Remove from heat and break up the crust with a spatula. Add sufficient 200 proof ethanol to cover the crust. Cover the beaker with Parafilm and let it sit O/N at RT. Pour off the ethanol into a clean beaker and put to the side. Add fresh ethanol to cover the crust. Repeat O/N extractions 3 times. Pool the extracts.
17. Use a vacuum pump to dry the ethanol extracts. If a vacuum pump is not available, add the ethanol extract to a clean beaker and warm to 50 °C while stirring in a fume hood. NOTE: Once the ethanol has evaporated a sticky residue of light brown color should remain. If heating is used, care should be taken to not burn the solution by heating for too long.
18. Dissolve residue in 10 ml of distilled sterile water. Filter sterilize this solution with a 0.22 µm syringe filter and store at -20 °C in 1 ml aliquots. NOTE: 1 ml of water is used for dissolving the residue for every 100 ml of the original liquid nematode culture. For example, if one of the liquid culture flasks is discarded due to contamination, then adjust the amount of water used to dissolve the residue.

2. Determination of Pheromone Dose Response

1. Prepare dauer pheromone by making 6x 5 ml of NGM media with Noble agar, without peptone, and supplemented with 50 µg/ml streptomycin sulfate and a range of dauer pheromone (see recipe in Table 1)^{4, 19}. Mix components in a 13x100 mm glass culture tube, boil over a Bunsen burner, and then pour into 3 cm Petri dishes.
2. Weigh a microcentrifuge tube. Add 1 ml of O/N culture of E. coli OP50 to the tube and centrifuge at ~17,000 x g in a microcentrifuge tube. Remove all of the supernatant. Weigh the tube again and determine the weight of the bacterial pellet. Resuspend the pellet with M9 buffer (See recipe in Table 1) for a final concentration of 4% (^w/_v). Aliquot 10 µl of the bacterial suspension onto the center of each pheromone plate⁴. Store plates O/N at RT.
3. Pick 10-15 gravid N2 wild-type hermaphrodites one day after the molt into adulthood onto the pheromone plates⁴. Store the plates at 25 °C for 3 - 4 hr.
4. Pick off all of the adult hermaphrodites. Record the number of eggs laid for each plate. Seal the plates with Parafilm and return to 25 °C for 3 days¹⁷.
5. Count the percentage of dauers (Figure 2). Note: For both methods it is important to note that dauers (and to a lesser extent non-dauers) will climb up the walls and onto the lid of Petri dishes. It is therefore important to examine all surfaces of the dish for nematodes.
6. Fit the data to a dose-response curve and estimate the EC₉₀ concentration of pheromone (sufficient pheromone to induce 90% of animals to form dauers) as shown in Figure 3. Note: We typically use a logistic regression model to estimate the EC₉₀, but different statistical software packages may have alternative methods that produce similar estimates.

3. Live Imaging of Dauer IL2 Neurons​

1. Prepare dauer pheromone plates as in protocol 2 using the EC₉₀ value determined in step 2.6.
2. Induce dauers using the methods in protocol 2 with a strain carrying an integrated IL2 reporter transgene (myIs13[P_klp-6::gfp], myIs14[P_klp-6::gfp], myIs16[P_klp-6::tdTomato] or qIs56[P_lag-2::gfp])^{12, 20, 21}. NOTE: If qIs56 is used, expression of GFP will not be visible in the IL2Qs until several hours into the dauer molt and some of the initial remodeling events will not be visible. Additionally, while the fluorescent signal from the P_lag-2::gfp transgene is ultimately brighter in the IL2s during dauer than the P_klp-6 fluorescentreporters, the P_lag-2::gfp transgene also expresses weakly in the head muscles which can mask the fine IL2 branches.
3. Following egg-laying, remove the adult hermaphrodites, seal the plates with Parafilm and incubate for 34 hr at 25 °C¹⁷. NOTE: The length of time to the dauer molt varies slightly among individuals. The most rapid period of dendrite arborization begins 4 - 5 hr following the onset of the dauer molt (39 - 44 hr post egg-laying at 25 °C)¹².
4. The day before imaging, make up a solution of 10% (^w/_v) agarose in M9 buffer with dauer pheromone at the EC₉₀ concentration. Aliquot approximately 100 µl of agarose onto a microscope slide and quickly, but gently, place another slide on top to create a flat agarose surface. After the agarose has solidified, wrap the slides in saran wrap and store in a humidity chamber (pipette tip box with wet paper towels).
5. After the 34 hr incubation period, examine pheromone plates for nematodes that have stopped pharyngeal pumping. Separate slides such that only one surface of one slide has agarose on it. Pick one or more nematodes onto a 10% agarose pad and 1 µl of 0.1 micron polystyrene beads²². NOTE: With a well-synchronized population, the majority of the nematodes on the plate will be entering into the molt from L2d to dauer. However, there may be variation among individuals. It is therefore important to note additional features (stoma occlusion, pharyngeal remodeling) to estimate the amount of time the animals have been within the dauer molt (see representative results for example).
6. Determine the orientation (left/right, dorsal/ventral) of the nematode. Capture Z-stack images of an IL2Q dendrite at 100x magnification with the lowest possible fluorescence intensity every 15 min or as needed for the specific experiment. Continue capturing images until the nematode has separated from the L2d cuticle and immobilization is impossible or if the animal recovers from dauer (pharynx begins pumping). When not actively imaging, place the slide in a humidity chamber. NOTE: We use an epifluorescent microscope with a motorized stage and differential interference contrast (DIC) optics.

Results

The production of crude dauer pheromone results in a yellow liquid (Figure 1) that is both heat and cold stable. Aliquots of crude pheromone are stored at -20 °C indefinitely with no obvious loss in activity. Following the production of pheromone, a single dose-response bioassay is sufficient for a rough estimate of potency. However, for most experiments it is necessary to repeat the bioassay 2 - 3 times and take an average from each experiment. Representative results from two pheromone bioassays are giv...

Discussion

An examination of dauer-specific neuroplasticity and other dauer-associated morphological changes requires controlled and reliable formation of dauers either through genetic mutation (i.e., daf-c mutants) or by exposure of wild-type animals to pheromone. While the use of a genetic mutation to induce dauers is convenient, it may confound results. Therefore data collected with daf-c mutations should be subsequently confirmed with wild-type animals induced to enter the dauer stage by exposure to d...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
N2 C. elegans Bristol strain	Caenorhabditis Genetics Center
PT2660 myIs13[Pklp-6::gfp] III	Upon request from Schroeder lab
PT2762 myIs14[Pklp-6::gfp] V	Upon request from Schroeder lab
JK2868 qIs56[Plag-2::gfp] V	Caenorhabditis Genetics Center
OP50 E. coli	Caenorhabditis Genetics Center
Petri dishes	Tritech Research	60 mm T3308, 35 mm T3501
NGM agar	Various		3 g NaCl, 17 g agar, 2.5 g peptone in 975 ml H2O autoclaved cooled to 55°C followed by 1 ml of 5 mg/ml cholesterol in ethanol, 25 ml of 1 M KPO4 buffer (pH 6.0), 1 ml of 1 M CaCl2, 1 ml of 1 M MgSO4
S Media	Various		S media consists of S basal solution (1.46 g NaCl, 0.25g K2HPO4, 1.5 g KH2PO4, 0.25 ml of 5 mg/ml cholesterol in ethanol and H2O to 250 ml. Autoclaved.) To the S basal solution add 2.5 ml of potassium citrate pH 6.0 (2 g citric acid monohydrate, 29.4 g tri-potassium citrate monohydrate, H2O to 100 ml, autoclaved), 2.5 ml of Trace Metals Solution (1.86 g disodium EDTA, 0.69 g FeSO4 •7 H2O, 0.2 g MnCl2•4 H2O, 0.29 g ZnSO4 •7 H2O, 0.025 g CuSO4 •5 H2O, H2O to 1 L. Autoclaved and stored in the dark), 0.75 ml of 1 M CaCl2, and 0.75 ml of 1 M MgSO4.
Dauer pheromone plates for dose-response assay	Various		Mix 0.085 g Noble agar, 0.5 ml of 0.513 M NaCl and 5 µl of 5 mg/ml cholesterol dissolved in ethanol in each of 6x 15 ml culture tubes. Add sufficient crude pheromone to each tube to create a range of concentrations. Add H2O to bring the volume to 4.725 ml.  Boil over a Bunsen burner until the agar is dissolved and then cool to 55 °C. Add 125 µl 1 M KPO4 buffer (pH 6.0), 50 µl 0.1 M CaCl2, 50 µl 0.1 M MgSO4 and 50 µl of 5 mg/ml streptomycin sulfate to each tube.  Pour the contents of each tube into a 35 mm diameter Petri dish. Let the agar solidify at room temperature overnight (if longer, store in enclosed container to prevent excessive drying).
Microsphere beads 0.1 micron	Polysciences Inc.	00876-15
M9 buffer	Various		Mix 3 g KH2PO4, 6 g Na2HPO4, 5 g NaCl, 1 ml 1 M MgSO4, H2O to 1 liter. Sterilize by autoclaving