All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.
1. Staining of Hemocytes
- Immunostaining with an anti-Croquemort antibody
- Serially soak glass slides in methanol for 10 min, in PBS containing 0.2% (v/v) Triton X-100 for 10 min, and then in PBS for 10 min.
- Mount 20 µL of 5% (v/v) whole swine serum in PBS containing 0.2% (v/v) Triton X-100 on cells for blocking. Incubate slides at room temperature for 20 min.
- Remove the solution from glass slides, and mount 20 µL of anti-Croquemort antiserum (0.1% (v/v)) in PBS containing 0.2% (v/v) Triton X-100 on cells. Incubate slides at 4 °C overnight.
- Soak glass slides in PBS containing 0.2% (v/v) Triton X-100 for 10 min 5 times.
- Soak glass slides in PBS for 10 min.
- Mount 20 µL of alkaline phosphatase-labeled anti-rat IgG (0.5% (v/v)) in PBS containing 0.2% (v/v) Triton X-100 and 5% (v/v) whole swine serum on cells at room temperature for 1 h.
- Soak glass slides in PBS containing 0.2% (v/v) Triton X-100 for 10 min 5 times.
- Soak glass slides in buffer containing 100 mM Tris-HCl, pH 9.5, 100 mM NaCl, and 50 mM MgCl2 for 10 min.
- Mount phosphatase substrate solution containing 0.23 mg/mL 5-bromo-4-chloro-3-indolyl-phosphate (BCIP), 0.35 mg/mL nitro blue tetrazolium (NBT), 100 mM Tris-HCl, pH 9.5, 100 mM NaCl, and 50 mM MgCl2 on cells.
- Observe cells under a microscope for proper staining. When strong purple signals appear in the granules of hemocytes, remove the substrate solution, and soak glass slides in buffer consisting of 10 mM Tris-HCl, pH 8.5, and 1 mM EDTA. Staining for approximately 5 - 10 min is recommended.
2. Stain Apoptotic Cells by TUNEL
- Soak glass slides in PBS for 5 min.
- Repeat with new PBS.
- Mount Equilibration buffer (See Materials Table) on cells for 10 min.
- Remove the solution from glass slides, and mount 20 µL of TdT solution containing 5 µL of terminal deoxynucleotidyl transferase and 15 µL of Reaction Buffer on cells at 37 °C for 1 h.
- Remove the solution from glass slides, and soak slides in buffer consisting of 0.5 mL STOP/Wash buffer and 17 mL of water.
- Soak slides in PBS for 5 min 3 times.
- Mount 20 µL of Anti-Digoxigenin-Peroxidase on cells at room temperature for 30 min.
- Soak glass slides in PBS for 5 min 4 times.
- Soak glass slides in peroxidase substrate solution consisting of 30 mL of 50 mM Tris-HCl, pH7.5 containing a full micro spatula of 3,3'-diaminobenzidine tetrahydrichloride (DAB), and 0.002% (v/v) H2O2 for 30 s.
- Repeat the above step until apoptotic cells are stained brown. Soak glass slides in water to stop the peroxidase reaction.
- Enclose cells with water for observation.
3. Measure the Level of Phagocytosis of Apoptotic Cells
- Observe samples under a light microscope in order to assess the level of phagocytosis. Count Croquemort-positive cells or GFP-positive cells as hemocytes, TUNEL-positive cells as apoptotic cells, and double-positive cells as phagocytosing hemocytes.
- The phagocytic index is defined as the number of double-positive cells to the total number of Croquemort-positive cells or GFP-positive cells. It is recommended that more than 300 hemocytes are observed.