Using Eggs from Schistosoma mansoni as an In vivo Model of Helminth-induced Lung Inflammation

1. Purifying Schistosoma mansoni Eggs

1. Infect Swiss-Webster mice with schistosome cercariae, which is the infectious stage in the Schistosoma life cycle ⁸. Alternatively, obtain schistosome-infected mice from the NIAID Schistosomiasis Resource Center (http://www.schisto-resource.org/). Leave mice for 6-7 weeks following infection, by which time-point, eggs are present in the liver and can be recovered as described below (See Fig. 1).
2. Euthanize mice with CO₂, and wet with 70% ethanol. Place mouse on back. Use blunt forceps and scissors to cut away skin and underlying peritoneum. Excise the liver, located below the ribcage and diaphragm.
3. Finely mince livers and add 20 mL per liver of digestion mixture, composed of collagenase/dispase (0.5 mg/mL), penicillin (100 U/mL) and streptomycin (100 μg/mL) in PBS. Put mixture in a 50 mL Falcon tube and incubate overnight in a 37 °C shaker.
4. Centrifuge mixture at 400 x g / 3 min / 20 °C. Gently pour off excess liquid and fill tube with PBS. Centrifuge again and repeat PBS wash. Following last centrifugation, resuspend pellet in 25 mL PBS.
5. Strain the resuspended pellet through a standard kitchen metallic strainer (use a 50 mL syringe plunger to mash the liver pieces through into a glass beaker), followed by passing the mixture through a fine sieve (use 10 mL syringe to push mixture through the fine sieve into a second glass beaker).
6. Put strained mixture in a 50 mL Falcon tube. Centrifuge at 400 x g / 5 min / 20 °C. Carefully pour out supernatant without losing pellet. Resuspend pellet in 3 mL PBS.
7. Overlay mix gently onto a 20% Percoll, 40 mL gradient of 8 mL Percoll and 32 mL 0.25M sucrose (FW=342.3 so 8.56 g sucrose/100 mL H₂0).
8. Centrifuge 10 min / 800 x g / 20 °C. Pipette off and discard gelatinous top layer of liver cells. Remove egg pellet at bottom with a transfer pipette and put into a 15 mL Falcon tube.
9. Wash pellet 3X in 10 mL PBS/1 mM EDTA/1 mM EGTA using centrifuge settings: 3 min / 30 x g / 20 °C. Resuspend in 500 μL PBS.
10. Overlay mix on a new 25% Percoll, 10 mL gradient (2.5 mL Percoll and 7.5 mL 0.25M sucrose) using centrifuge settings: 10 min / 800 x g / 20 °C.
11. Wash 3X in 10 mL PBS using centrifuge settings: 3 min / 30 x g / 20 °C.
12. In the last 10 mL wash, remove 100 μL to count eggs. Eggs settle quickly, so the Falcon tube must be mixed well before removing sample. Dilute the 100 μL sample with 900 μL PBS. 100 μL of the mix should be counted as droplets on a microscope slide using a dissecting microscope (1:10 dilution). Wide-bore pipette tips should be used.
13. Resuspend eggs at 50,000 eggs/mL in PBS. Eggs can be stored for several months at -80 °C and thawed once or twice for use. Before use, inspect under a microscope to ensure that eggs are still intact (see Fig. 1).

2. Intraperitoneal Sensitization with S. mansoni Eggs: Day 0

1. Prepare eggs at 5,000 eggs/100 μL PBS in a 5 mL snapcap tube. For injection, estimate 50% more eggs than necessary.
2. Load a 23 gauge^3/4inch needle and a 1 mL syringe with 100 μL of egg suspension per mouse. Eggs settle, so load needle with eggs immediately prior to use.
3. Rock syringe back and forth to mix eggs prior to each injection, and inject intraperitoneally 100 μL of suspension per mouse.

3. Retro-orbital Intravenous Challenge with S. mansoni Eggs: Day 14

1. Prepare eggs as above at 5,000 eggs/100 μL.
2. Anesthetize mice in specialized chamber with isoflurane (4%), or intraperitoneally with xylazine (10 mg/kg) and ketamine (120 mg/kg). Depth of anesthesia is determined by pinching of the footpad and ensuring no physical response.
3. Following loading of the 1 mL syringe and 23 gauge^3/4inch needle with eggs, use forceps to bend the needle at a 90° angle with the bevel facing down into the angle. Ensure that no bubbles are present.
4. Place mouse on one side. Retract skin so eye will protrude, and inject 100 μL into the vessels behind the eyeball at a 45° angle to the nose.
5. Withdraw needle and apply light pressure to control bleeding.

All of these procedures must be carried out with care, and mice must be monitored until they recover from anesthesia. These protocols were approved by the University of Pennsylvania Institutional Animal Care and Use Committee (IACUC).

4. Experimental Harvest: Day 22

1. Euthanize mice with CO₂.
2. Wet mouse with 70% ethanol, and place on back.
3. Using blunt forceps, grasp the mouse abdomen and make a small incision in the skin. Carefully remove skin with scissors and expose the rib cage and peritoneum.
4. Cut open the peritoneum. Cut the abdominal aorta to recover the blood with a Pasteur pipette. Store on ice.
5. Move the liver down to expose the diaphragm. Use fine scissors to cut the diaphragm. Carefully cut open the rib cage to expose the lung tissue.
6. Recover the parathymic lymph nodes that drain the lung with fine forceps. These are tucked underneath the rib cage, on either side of the thymus ⁹. Store on ice in 1mL sterile media (DMEM supplemented with 10% heat-inactivated fetal calf serum, 100 U/mL penicillin, 100 μg/mL streptomycin, 2 mM L-glutamine, 50 μM 2-mercaptoethanol, all available from Invitrogen).
7. To recover the BAL, and inflate the lungs for histologic analysis, intratracheal intubation must be performed. Expose the trachea by moving the salivary glands to the side, and placing fine forceps under the trachea. Using fine scissors, cut a hole in the middle of the trachea, and insert tubing into the lungs. Secure tubing by tying with surgical thread.
8. Attach PBS-filled 1 mL syringe to the tubing and inflate lungs with 1 mL PBS. Carefully retrieve BAL wash with syringe. Store on ice.
9. Attach 4% paraformaldehyde (PFA) in PBS-filled 1 mL syringe to the tubing and inflate the lungs.
10. Remove the tubing, and tighten the surgical thread to prevent leaking of the PFA.
11. Carefully dissect out lung tissue and place in a 50 mL Falcon tube with 5 mL 4%PFA.

5. Preparation of Recovered Tissues

1. Serum: Following storage on ice for 30 min to 2 h for blood to clot, serum is recovered from the blood by centrifugation (13000 x g / 10 min / 4 °C). Serum is stored at -20 °C and can be used for cytokine ELISAs or S. mansoni egg antigen-specific IgG isotype ELISAs ^{6, 10}.
2. Lymph Nodes: Single cell suspensions are prepared and cell counts used to evaluate the magnitude of the immune response. To examine Th2 cell polarization, cells are re-stimulated with S. mansoni egg antigen for 72 hours. Intracellar cytokine staining can be examined by flow cytometry, and supernatants can be recovered and stored at -20 °C for ELISA of Th2 cytokines (IL-4, IL-5, IL-13) ⁶.
3. BAL: Cells are pelleted (400 x g / 5 min / 4 °C). BAL fluid is recovered and stored at -20 °C for analysis of Th2 cytokines by ELISA. BAL cells counts are used as a readout for airway inflammation. Cytocentrifuge preparations of 10,000-100,000 cells (500 rpm / 5 min / 4 °C), followed by Diffquik staining will allow enumeration of inflammatory infiltrate ^{4, 6}. Alternatively, BAL cells can be examined by flow cytometry ⁶.
4. Lung tissue: Lung tissue is stored overnight at 4 °C. Fixed tissue is paraffin-embedded, sectioned and mounted on slides for histological and immunofluorescence analysis.

6. Representative Results

This protocol details all the steps necessary to (i) prepare purified Schistosoma mansoni eggs for in vivo use (Fig. 1), (ii) sensitize and challenge mice with these eggs and (iii) recover organs for examination of the lung inflammatory response. This in vivo model reproducibly drives a potent Th2 lung inflammatory response. This is shown by airway inflammation and eosinophilia as visualized by BAL cell counts and cytocentrifuge preparations (Fig. 2). H&E-stained lung sections can be examined for egg-induced granulomas (Fig. 3a), and immunofluorescent staining of lung sections allows visualization of alternatively activated macrophages and Th2 cytokine-induced genes such as Resistin-like molecule (RELM) α (Fig. 3b). The antigen-specific CD4 Th2 cytokine response is examined by ELISAs for IL-5, IL-4 and IL-13 of antigen-stimulated parathymic lymph node cells (Fig. 4).

Figure 1. Schistosoma mansoni egg injection model. Representative pictures of granulomatous livers, characteristic of high S.mansoni-egg burdens, and of S.mansoni eggs are shown – average size (L) 120 μm by (W) 50 μm.

Figure 2. S. mansoni egg injection drives airway inflammation. A. BAL cell numbers (x10⁵) from naïve (N) or S.mansoni (Sm) egg-injected mice. *P<0.05. B. Cytocentrifuge preparation of BAL cells. Mac, MACROPHAGE; Eos, EOSINOPHIL; LYMPH, lymphocyte. Bar, 10 μm.

Figure 3. Visualization of pulmonary granulomas and alternatively activated macrophages surrounding the S.mansoni egg. A. Pulmonary granuloma surrounding the Sm egg (black arrow) was visualized in H&E-stained lung sections. B. Immunofluorescence staining for RELMα (green), mannose receptor (red) and DAPI (blue) reveals alternatively activated macrophages (white arrow) in the granuloma surrounding the autofluorescent Sm egg (black arrow). Bar, 50 μm.

Figure 4. S.mansoni egg antigen-specific Th2 cytokine response. Draining parathymic lymph node cells from naïve (N) or Sm egg-injected mice were stimulated with Sm egg antigen for 72 hours, followed by ELISA of supernatants for IL-4, IL-5 and IL-13. Scale, ng/mL.*P<0.05.