Procedure for Culturing BG01V Human Embryonic Stem Cells
Introduction
Human embryonic stem (hES) cells are pluripotent stem cells derived from pre-implantation embryos that can be maintained and expanded in an undifferentiated state or induced to differentiate along somatic or germ cell lineages. They can be maintained either on a layer of mitotically inactivated human or mouse feeder cells (1) or using mouse or human feeder cell conditioned medium (2) (R&D Systems, Catalog # AR005 or AR007, respectively). The protocol below has been used with the BG01V line of hES cells (3, 4).
Please note that other hES cell lines may require modifications of this protocol. Optimal culture conditions must be determined by the investigator for each hES line.
Materials Required
Reagents:
Recombinant human FGF basic (R&D Systems, Catalog # 233-FB, 4114-TC, or equivalent)
Accutase (Innovative Cell Technologies, Catalog # AT104 or equivalent)
Cultrex® Basement Membrane Extract (BME) (R&D Systems, Catalog # 3433-005-01 or equivalent)
DMEM/F12 (Invitrogen, Catalog # 12500-096 or equivalent)
Materials:
BG01V human embryonic stem cells
Tissue culture dishes (60 mm; Fisher, Catalog # 08-772B, 100 mm; Fisher, Catalog # 08-772E, or equivalent)
15 mL conical tubes (Corning Costar, Catalog # 430052 or equivalent)
Pipettes and pipette tips
Equipment:
37° C and 5% CO2 humidified incubator
Centrifuge (low speed clinical or equivalent)
Hemacytometer
Inverted microscope
Procedure
Thawing and Expanding Cryopreserved Cells:
Prepare the desired number of plates by coating with Cultrex BME as described above, 1 - 2 hours prior to passaging the cells.
Warm the Human Feeder Cell Conditioned Medium to 37° C.
Remove the Human Feeder Cell Conditioned Medium from the cells. Add 1 mL of Accutase solution to each 60 mm plate. Incubate at room temperature for 5 - 10 minutes or until the cells begin to slough off the plate.
Pipette gently over the plate until all the cells have been detached.
Pipette the cell suspension up and down to break up large cell clumps.
Remove the cell suspension to a 15 mL conical tube containing 5 mL of Human Feeder Cell Conditioned Medium and spin at 200 x g for 4 minutes.
Resuspend the pellet in Human Feeder Cell Conditioned Medium and count the cells using a hemacytometer.
Plate the desired number of cells (approximately 1.0 x 106 cells/60 mm plate) on the Cultrex BME coated plate in Human Feeder Cell Conditioned Medium containing 4 ng/mL of rhFGF basic.
Change the medium daily. Monitor the cells for the desired confluency.
Warm the Human Feeder Cell Conditioned Medium to 37° C.
Thaw the vial of BG01V hES cells by warming until just thawed and then immediately transfer to a 15 mL conical tube containing at least 5 mL of pre-warmed Human Feeder Cell Conditioned Medium.
Spin at 200 x g for 4 minutes.
Remove the supernatant and gently flick the pellet. Resuspend the pellet in an appropriate amount of Human Feeder Cell Conditioned Medium supplemented with 4 ng/mL of recombinant human FGF basic.
Add the BG01V hES cell suspension to the Cultrex BME coated plate.
Grow in the 37° C, 5% CO2 incubator. Change the medium daily and monitor the cells. Passage the cells at the desired confluency.
Thaw Cultrex BME on ice at 2 - 8° C overnight.
Aliquot thawed Cultrex BME into pre-cooled tubes and store at = -20° C.
Thaw the aliquot on ice at 2 - 8° C overnight.
Dilute Cultrex BME 1:40 in DMEM/F12. This can be stored for up to 2 weeks at 2 - 8° C.
Coat the desired number of plates with diluted Cultrex BME (approximately 2.5 mL per 60 mm plate) and incubate for 1 - 2 hours at room temperature.
Remove the Cultrex BME solution immediately prior to plating the cells.
Prepare the Cultrex BME coated plate.
Thawing of BG01V hES Cells:
Passaging of BG01V hES Cells:
References
Thomson, J.A. et al. (1998) Science 282:1145.
Xu, C. et al. (2001) Nature Biotechnology 19:971.
Zeng, X. et al. (2004) Restor. Neuro. Neurosci. 22:421.
Plaia, T. et al. (2006) Stem Cells 24:531.
