A Method for 3D Bioprinting Murine Cortical Astrocytes
筆記録
To obtain a final concentration of 1 x 106 cells per milliliter, transfer 1 milliliter of gelatin-gelatin-methacryloyl-fibrinogen solution to the tube containing the cells, and homogenize by gently pipetting up and down. Use a 1000-microliter pipette to slowly transfer the astrocytes laid in gelatin-gelatin-methacryloyl-fibrinogen bioink solution to a 5-milliliter plastic syringe, avoiding bubble formation. Connect a sterile 22-gauge blunt needle to the syringe.
Expose the bioprinter to UV light for 15 minutes, and then wipe the bioprinter with 70% ethanol. Then connect the syringe to the bioprinter print head, and manually flush the bioink to remove the remaining bubbles.
To conduct bioprinting, place a 35-millimeter culture dish on the bioprinter table. Position the needle 0.1 millimeters away from the culture dish surface to allow movement of the needle, and press the 印刷 button. Once the bioprinting is over, ensure that the syringe moves away from the dish, and close the culture dish. Place the culture dish under UV light for gelatin-methacryloyl cross-linking.
Use a sterile spatula to transfer the bioprinted construct to a 24-well plate, add 500 microliters of thrombin calcium chloride solution, and leave for 30 minutes to allow fibrin cross-linking. After removing the cross-linking solution, wash the construct with 2 milliliters of PBS. Then, replace the PBS with 1 milliliter of astrocyte culture medium. Incubate at 37 degrees Celsius and 5% carbon dioxide, and change the medium every three days.
