1. Organoid Processing for Histology: The Agarose Spin Down Method
NOTE: This protocol is adapted from a previous publication by Vlachogiannis et al. We have added a step involving agarose embedding to embed all populations of organoids successfully.
- Remove existing media from the well. Be careful not to aspirate the basement membrane domes.
- Add an equal (equal to the volume of media removed from step 1) volume of cell recovery solution and incubate for 60 min at 4 °C.
- Dislodge the basement membrane dome using a pipette and crush the basement membrane dome using a pipette tip. Collect the dissociated dome and cell recovery solution in a 1.5 mL tube.
- Centrifuge at 300 x g and 4 °C for 5 min.
- Remove the supernatant (cell recovery solution). Save all supernatants in separate tubes until the end, when the presence of organoids is confirmed in the final pelleting step.
- Add desired volume (Table 1) of cold PBS and gently pipette up and down to disturb the pellet mechanically.
- Centrifuge at 300 x g and 4 °C for 5 min.
- Remove the supernatant (PBS).
- Fix the pellet in a matched volume (e.g., 500 µL for one pellet from the 24-well plate culture condition, Table 1) of 4% PFA for 60 min at room temperature.
- Following fixation, centrifuge at 300 x g and 4 °C for 5 min.
- Remove the supernatant (PFA).
- Wash with matched volume (e.g., 500 µL for one pellet from the 24-well plate culture condition, Table 1) of PBS and centrifuge at 300 x g and 4 °C for 5 min.
- Prepare warm agarose (2% agarose in PBS).
NOTE: Here, cell pellets for frozen sections can be directly resuspended in 200 µL of OCT compound.
- Resuspend the cell pellet in 200 µL of agarose (2% in PBS).
- Immediately after adding agarose, gently detach the cell pellet from the wall of the 1.5 mL tube using the 25 G needle attached to the 1 mL syringe. As shown in Figure 1, if the cell pellet is not physically detached from the wall of the 1.5 mL tube, then there is a risk of losing all or part of the cell pellet during the agarose embedding process.
- Wait until the 2% agarose in PBS is completely solidified.
- Detach the solidified agarose block from the 1.5 mL tube using a 25 G needle attached to the 1 mL syringe.
- Transfer the detached agarose block containing the cell pellet to a new 1.5 mL tube.
- Fill the tube with 70% EtOH and proceed further using the conventional protocol for tissue dehydration and paraffin embedding.
Table 1: Seeding density, basement membrane volume, and medium volume needed for one dome
| Culture Plate | Seeding Density (cells) | Basement Membrane Volume (μL) | Medium (μL) |
| 48 well | 25,000-50,000 | 20 | 250 |
| 24 well | 50,000-250,000 | 40 | 500 |
| 6 well | 50,000-250,000 | 40 | 2,000 |