Expansion of mouse embryonic fibroblasts (MEFs) for hPSC cultures

Hanqin Li, Oriol Busquets, Steven Poser, Dirk Hockemeyer, Frank Soldner

Published: 2022-09-07 DOI: 10.17504/protocols.io.b4n5qvg6

Abstract

This protocol describes the expansion of mouse embryonic fibroblasts (MEFs) as feeder cells for human pluripotent stem cell (hPSC) culture.

General notes

  1. Throughout this protocol, the term hPSC is used to collectively refer to both hiPSCs and hESCs. All described procedures have been tested and work equally well for hiPSCs and hESCs.

  2. MEFs were obtained as described in Manipulating the Mouse Embryo: A Laboratory Manual, Third Edition (ISBN: 0879695919)

Citation
Andras Nagy, Marina Gertsenstein, Kristina Vintersten, & Richard Behringer Manipulating the Mouse Embryo: A Laboratory Manual, 3rd ed. Cold Spring Harbor Laboratory Press

Before start

All cell culture plates which are used as feeders to maintain hPSCs are coated for at least 1 hour with autoclaved 0.2% gelatin solution at room temperature. Remove gelatin solution immediately before plating MEF cells.

0.2% Gelatin Solution

AB
Sterile H2O1L
Gelatin powder2g

After preparation, the gelatin solution should be autoclaved. Final volume: 1L

Steps

1.

Wash the plates twice with DPBS

2.

Add Trypsin and incubate for 0h 5m 0s (37°C; 5% CO2)

3.

Add MEF medium to neutralize the Trypsin and collect the solution into a conical tube.

3.1.

MEF medium

AB
DMEM435 ml
FB Essence/FBS*75 ml
200mM L-Glutamine5 ml
Penicillin & Streptomycin (100x)5 ml
MEM Non-Essential Amino Acids5 ml

*We have successfully used either FB Essence or FBS and have not observed an obvious difference. Final volume: 500ml

4.

Centrifuge at 250x g

5.

Remove the supernatant. Re-suspend the cell pellet in fresh MEF medium to plate on gelatin-coated plates (Dilution ratio 1:4) and maintain in a humidified incubator (37°C; 5% CO2).

6.

MEFs need to be passaged once confluent (every 3-4 days) and can be expanded up to passage 4 (P4) and frozen before or after inactivation using irradiation or Mitomycin C treatment.

For more information on freezing MEFs, as well as irradiation and Mitomycin C treatment of MEFs, refer to the collection "Maintenance and inactivation of mouse embryonic fibroblasts (MEFs) as feeder cells for human pluripotent stem cell culture." A link to this collection can be found in the title section of this protocol, located above

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