Investigating Target Gene Function in a CD40 Agonistic Antibody-induced Colitis Model using CRISPR/Cas9-based Technologies

All animal experiments performed following this protocol must be approved by the respective Institutional Animal Care and Use Committee (IACUC). All procedures described here were approved by the AbbVie IACUC.

1. Generation of required lentiviruses and procurement of donor and recipient animals

NOTE: The Table of Materials includes source and order number details for all animals, instruments, and reagents used in this protocol.

1. Construct the plasmids using a lentiGuide-puro vector modified to VexGFP or mCherry.
   1. Clone the scrambled non-targeting gRNA (SgNone) or CD40-targeting gRNA into the modified vector.
      ​NOTE: In this study, the sequences for each gRNA were as follows: SgNone, CTATGATTGCAACTGTGCAG; SgCD40.1, AGCGAATCTCCCTGTTCCAC; SgCD40.2, GACAAACAGTACCTCCACGA; and SgCD40.3, ACGTAACACACTGCCCTAGA.
   2. Produce the lentiviral particles as described previously¹⁵.
      1. Co-transfect the gRNA-encoding plasmids into 293T cells with VSV-G and pLEX packaging plasmids.
      2. Change the culture medium after 18 h of transfection, and collect the supernatants containing the virus after 24-48 h following the medium change.
      3. To evaluate CD40 gRNA efficiency, generate a CD40 stable 293T cell line by transfection of a pcDNA3.1 plasmid that encodes for CD40.
   3. Transfect the cells using the described lentiviruses, and evaluate them by fluorescence-activated cell sorting (FACS) two weeks later.
      NOTE: Cas9 KI mice were used as donor mice. Ensure that the Cas9 KI mice are on a C57Bl/6 background (and are expressing the CD45.2 allele) when using C57Bl/6-Ly5.1 Pep Boy mice (expressing the CD45.1 allele) as recipients, so GvHD is avoided and to track donor and recipient cells.
2. Design the experiment. For gene knockout (KO), use 3-6 gRNAs per gene. For each gRNA, prepare 20% extra recipient mice to account for animal loss during and after transplantation.
   ​NOTE: The CD40 agonistic antibody-induced colitis model requires a minimum of 8 mice per group for statistical powering. Hence, 10 mice per gRNA were prepared in this study. The number of mice needed for other in vivo models will vary based on the model used.
3. Use same sex donor and recipient mice that are 8-12 weeks of age.
   NOTE: Mice were euthanized under IACUC approved guidelines using a minimum 5% isoflurane and confirmed with cervical dislocation as a secondary method.

2. Bone marrow harvest and preparation for cell sorting

1. Using forceps and scissors, harvest bones from each donor mouse (femur, tibia, humerus, and ulna), carefully removing as much muscle/tissue as possible.
2. Puncture the bottom of a 0.6 mL microcentrifuge tube with a 23 G needle, and place the tube inside a 1.5 mL centrifuge tube. Make 2 sets per animal.
3. Cut one end of the bones open, and place 4-8 bones inside the microcentrifuge tube with open ends facing toward the 23 G needle hole.
   NOTE: The number of bones per tube depends on the bone, e.g., 8 tibiae, humeri, and ulnae or 4 femurs will fit.
4. Centrifuge the tubes (with the 0.6 mL microcentrifuge tube containing the bones inside the 1.5 mL centrifuge tube) at 300 × g for 2 min at room temperature (RT).
5. Discard the 0.6 mL microcentrifuge tube, now containing bones with no marrow, leaving just the 1.5 mL centrifuge tube now full of marrow. Add 1 mL of red blood cell lysis buffer (containing ammonium chloride) to each centrifuge tube, and resuspend the cell pellet by pipetting. Incubate at RT for 1 min. Repeat the lysis step if needed.
6. Transfer the cell suspension into a 50 mL conical tube, and add Dulbecco's phosphate buffered saline (DPBS) without calcium and magnesium (at least double the volume of the cell suspension) to neutralize the lysis buffer. Pellet cells at 300 × g for 5 min. Aspirate the supernatant completely.
7. Load a 70 µm filter on a 50 mL conical tube, and filter the cells through, using DPBS to wash the tube and filter. Discard the filter, and count the cells.
   ​NOTE: Using 30 donor mice (12 weeks old) will yield 200-300 × 10⁶ cells on average.

3. Cell sorting to isolate LSK cells for transduction

1. Re-suspend the cells counted in step 2.7 in magnetic cell sorting (MACS) buffer (DPBS, 2 mM ethylenediamine tetraacetic acid, 0.5% bovine serum albumin, 10 µg/mL penicillin-streptomycin) in the desired volume (90 µL per 10⁷ cells).
2. Add 10 µL of CD117+ beads per 10⁷ cells. Mix well, protect from light, and incubate at 4 °C for 15 min.
3. Prepare the MACS LS column by placing the column in the magnetic field and rinsing it with MACS buffer.
4. Wash the cells from step 3.2 with an appropriate volume of MACS buffer (at least double your volume), and centrifuge at 300 × g for 10 min.
5. Aspirate the supernatant completely. Re-suspend the pellet so that the final concentration is 10⁸ cells in 500 µL of MACS buffer.
6. Apply the cell suspension onto the LS column. Wash with 3 times with 3 mL of MACS buffer.
   NOTE: One LS column can take up to 10⁸ labeled cells and 2 × 10⁹ total cells.
7. Remove the column from the magnetic separator, and place it in a suitable collection tube. Add 5 mL of MACS buffer, and immediately flush out the magnetically labeled cells by firmly pushing the plunger into the column.
8. Pellet the cells at 300 × g for 10 min. Aspirate the supernatant completely.
9. Re-suspend the cells in 100 µL of MACS buffer per 10⁷ cells, and add the staining antibodies for lineage (CD3, B220, Ter119, Gr-1, CD11b) and Sca-1.
   NOTE: Using 30 donor mice (12 weeks old) will yield 100-180 × 10⁶ cells on average.
10. Mix well, protect from light, and incubate at 4 °C for 20 min.
11. Wash the cells by adding 5-10 mL of MACS buffer, and centrifuge at 300 × g for 10 min. Aspirate the supernatant completely.
12. Re-suspendup to 10⁸ cells in 500 µL of MACS buffer
13. Filter the cells with a 70 µm cell strainer, and perform FACS for lineage-Sca1+ population.
    ​NOTE: Approximately 1.8-2.6% of the population should be lineage-Sca1+.
14. Collect the cells in LSK culture medium (100 µL per 10,000 cells): serum-free expansion medium, 100 ng/mL thrombopoietin, mouse stem cell factor, Fms-related tyrosine kinase 3 ligand, and IL-7 with 100 µg/mL penicillin-streptomycin.
15. Pellet cells at 300 × g for 10 min. Aspirate the supernatant completely.

4. LSK transduction and culture to generate control and knockout cells

1. Resuspend the cells in LSK culture medium.
2. Seed 10,000 cells per well in 96-well flat-bottom tissue culture (TC) plates in LSK culture medium.
3. Incubate overnight at 37 °C with 5% CO₂ and 95% humidity under aseptic conditions.
4. Prepare 50 µg/mL retronectin solution in DPBS, and add 300 µL to each well of a non-TC-treated 24-well polystyrene plate. Incubate overnight at 4 °C.
5. The next day, discard the retronectin solution, rinse the coated plate with 300 µL of DPBS, and repeat.
6. Transfer 50,000 LSK cells in 500 µL of medium (5 wells from the 96-well plate in step 4.2) to each retronectin-coated well of the 24-well polystyrene plate from step 4.4.Use an additional 100 µL of LSK medium per 5 wells to rinse and collect any extra cells remaining in the 96-well plate. Ensure that 600 µL is the volume per well in the 24-well plate following this step (5 × 100 µL wells from the 96-well plate + 100 µL used to wash those 5 wells).
   NOTE: After transferring, look under a microscope at the now empty 24 well plate to confirm that all cells were collected. Use LSK medium to collect cells that were not transferred to minimize cell loss from this small population.
7. Add 300 µL of virus supernatant to each well, and shake the plate at a setting value of 500 for 5 min. Spin the plate at 600 × g and 37 °C for 20 min. Use at least 5 × 10⁶ viral particles per mL.
   NOTE: In this study, a vector modified from pLentiPuro was used, in which the puromycin resistance element was swapped to VexGFP. The virus was added at a multiplicity of infection of 50-100.
8. Incubate for 1 h. Add 500 µL of pre-warmed LSK medium.
9. Incubate for 2 days at 37 °C with 5% CO₂ and 95% humidity under aseptic conditions.

5. Animal irradiation to prepare for donor stem cell engraftment

1. After 2 days of incubation, irradiate the recipient animals with 475 cGy twice at an interval of 4 h. Following the second round of irradiation, place the animals in autoclaved cages, and treat them as immunodeficient animals for 12 weeks. Mice received enrichment, hydrogel, and cage side monitoring to provide supportive care and intervention as needed. Mice may receive antibiotic food or water in addition to supportive care and intervention methods.
   ​NOTE. The irradiation dosages may differ with different irradiators. Perform a dose titration of the irradiator to identify the best dosage. Doses between 700 and 1300 cGy for C57Bl/6 mice are found to be effective in various literature examples¹⁷. Select 3-4 doses in this range, and evaluate 5 mice per dose for survival and engraftment. If engraftment is unsuccessful or the radiation dose is too high, mice will not live past 3 weeks post-engraftment. At 4 weeks post-engraftment, bleed the surviving mice to evaluate engraftment by FACS. We perform retro-orbital (RO) blood collections of ~50-100 µL per mouse to evaluate engraftment. Mice were under anesthesia (2-3% isoflurane) during collection and received eye lubricant and 1.0 mL subcutaneous saline as supportive care following RO blood collections.

6. Cell preparation and injection into irradiated recipient animals

1. Pipet the cells out of each well from step 4.9, keeping the groups separate now that the cells have been transduced with different gRNAs, and pellet them at 300 × g for 10 min.
2. Resuspend the cells in MACS buffer, filter with a 70 µm strainer, and sort the VexGFP+ population.
   NOTE: Approximately 10-15% of the cells should be VexGFP+.
3. Pellet the cells at 300 × g for 10 min. Resuspend them in Hank's balanced salt solution: 5,000 or more cells per mouse in 200 µL.
   NOTE: HBSS is non-pharmaceutical grade. You may also consider using a pharmaceutical grade sterile saline for injection.
4. Inject the cells intravenously 3 h after the last dose of irradiation.
   NOTE: Twelve weeks later, the mice will have a fully engrafted immune system and can be enrolled into in vivo models.

7. CD40 agonistic antibody-induced colitis model in wild-type mice

NOTE: Weigh and assess the animals daily. Provide supportive care as needed: 1.0 mL of subcutaneous sodium chloride solution at 10% weight loss or if they are dehydrated. The positive control for this model is anti-p40 dosed intraperitoneally at 25 mg/kg twice per week beginning on day -1.

NOTE: In this study, experimental groups included naïve control, vehicle (negative) control, and anti-p40 (positive) control groups. Together, these groups control for the normal behavior of the CD40 agonistic antibody-induced colitis model. Vector, SgNone, and SgRNA groups: The vector controls for the common lentiviral vector, SgNone is a scrambled non-targeting guide control, and the SgRNA groups are the "treatment" groups bearing reduced expression of the target gRNA.

1. Day 0: Inject CD40 agonistic antibody at 10 mg/kg intraperitoneally in DPBS into all animals except for naïve control.
2. Days 3 and 6: Perform video endoscopy to evaluate disease progression as previously described¹⁶.
   1. Anesthetize the mice with 2-3% isoflurane. Provide thermal support via internal anesthesia machine mechanism and/or external heat pad during recovery.
   2. Once the mice are under anesthesia, administer a DPBS (without calcium and magnesium) enema to prepare the colon for endoscopy.
      ​NOTE: Approximately 1-2 mL is required to perform an enema.
   3. After an enema and while under anesthesia, move the mouse to the nose cone of the anesthesia machine.
   4. Gently insert the endoscope into the colon, slowly advance to the proximal colon while keeping the camera centered and the colon inflated with air (using either the included air pump or attach a tube/syringe to manually inflate), then slowly withdraw the endoscope and collect a video and images at 3 cm, 2 cm, and 1 cm from the anus.
      NOTE: To minimize irritation of the colon, sterile lubricant may be added to the tip of the endoscope.
   5. Score each image individually based on the vascular pattern and thickening of the mucosa as described in Table 1. Combine the scores from the 3 images per mouse to assign a sum score to each animal.
3. Day 7: Euthanize all mice by isoflurane overdose or CO₂ chamber, and collect as much blood as possible by cardiac puncture for serum. Weigh the spleen to measure splenomegaly and collect for flow cytometry, and collect the colon for histopathology.
   NOTE: Formalin-fixed and paraffin-embedded tissue sections of mouse colon were prepared and used for immunohistochemistry (IHC) as previously described by Wang et al¹⁹.