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Table 2 Details of mouse pluripotent stem cell culture conditions. This table highlights that there are many variations on culture conditions for maintaining cells in distinct pluripotent states, including subtle differences in basal medium and cytokine concentrations that are often not emphasized. All culture medium formulations contain amino acids and 2-mercaptoethanol as standard. Pluripotency markers include Oct4, Sox2. Naïve pluripotency markers include Nanog, Rex1, Stella, Klf4, Esrrb. Primed pluripotency markers include Fgf5. Lineage markers include Brachyury, FoxA2, Eomes, Gata6, Gata4, Sox17. ‘Embryo-derived’ refers to cell lines that are directly derived from embryos, whereas ‘culture-derived’ refers to cell lines that are interconverted from different states e.g. changing the culture conditions of ESCs or EpiSCs

From: The many faces of Pluripotency: in vitro adaptations of a continuum of in vivo states

Cell type

Culture condition

Added factors

Basal medium

Embryo-derived

Culture- derived

Gene expression

X status

Functional tests

Ref.

Embryonic stem cells

(ESCs)

Feeders/ serum

-

MEFs/ DMEM/ 20% serum

 

Little transcriptional data

IVD, teratomas, pre-imp. Chimaeras, GLT

[4, 12]

Serum/LIF

1000 U/ml LIF

GMEM or DMEM/ 10% serum

 

Naïve markers. Heterogeneous lineage markers.

IVD, teratomas, pre-imp. Chimaeras, GLT.

[27, 28]

BMP/LIF

10 ng/ml BMP4

OR 200 ng/ml GDF6 + 1000 U/ml LIF

N2B27

Little transcriptional data. Homogeneous Oct4

 

Pre-imp. Chimaeras, GLT.

[29]

2i*

1 μm PD032/ 3 μM CHIR/ (+/− LIF)

N2B27

Homogeneous naïve markers. Reduced lineage markers (rel. to SL).

IVD, pre-imp. Chimaeras, GLT.

[91, 97]

KOSR/LIF

1000 U/ml LIF

Knockout DMEM/ 20% KOSR

Naïve and PrE markers

?

IVD, pre-imp. Chimaeras, GLT.

[46, 101]

Epiblast stem cells (EpiSCs)

F/A

5-12 ng/ml FGF2 + 10-20 ng/ml Activin

MEFs, Knockout DMEM/ 20% KOSR or “CDM” [207]

Primed markers. Heterogeneous lineage markers.

IVD, teratoma formation, rare pre-imp. Chimaeras, post-imp. Chimaeras.

[3, 17]

F4-EpiSC

25 ng/ml FGF4

DMEM/ 20% serum

 

Homogeneous Oct4. Primed and lineage markers.

Teratomas, pre-imp. Chimaeras.

[160]

F/A/XAV*

(WiEpiSC)

5 ng/ml FGF2/ 10 ng/ml Activin/ 10 μM XAV

DMEM/20% KOSR

Homogeneous pluri and primed markers. Reduced lineage markers (relative to FA).

?

Post-imp. Chimaeras –bias towards extraembryonic mesoderm.

[156]

F/A/IWP2*

(WiEpiSC)

12 ng/ml FGF2, 20 ng/ml Activin, 2 μM IWP2

Derivation in DMEM/ 18% KOSR/ 2% serum ➔ N2B27 at P2

 

Pluri markers. Reduced lineage markers (rel. to FA).

?

Enhanced ESC reversion, pre-imp. Chimaeras.

[127]

XAV/CHIR

3 μM CHIR/ 2 μM XAV

GMEM/ 10% serum

Reduced naïve markers (rel. to ESCs). Primed markers.

Teratomas formation.

[20]

Potential intermediate states

EpiLCs

12 ng/ml FGF2, 20 ng/ml Activin

N2B27/ 1% KOSR

 

Reduced pluri/naïve markers. Increased primed markers (rel. to ESCs). Reduced lineage markers (rel. to EpiSCs)

Efficient PGCLC generation.

[145]

Transient Epi state

10-12 ng/ml FGF2

N2B27 (+/− 1% KOSR)

 

Decreased Rex1, Increased Fgf5.

?

In vitro NMPs.

[154, 155]

INTPSC

12 ng/ml FGF2, 10 ng/ml Activin, 3 μM CHIR

N2B27/ 1% KOSR

 

Intermediate expression of pluri, naïve, primed and lineage markers.

Teratoma formation, pre-imp. Chimaeras.

[155]

FAB-SCs

1 ng/ml FGF2, 50 ng/ml Activin, 0.5 μM BIO, 100 ng/ml LIF blocking antibody

MEFS/ DMEM/ 15% KOSR

 

Pluri markers. Naïve miRNAs. Reduced naïve/germ cell markers (rel. to ESCs). Little/no primed expression.

?

Not functionally pluripotent

[161]

IESCS

12 ng/ml Activin

GMEM/ 10% serum

 

Intermediate expression of pluri, naïve, primed and lineage markers.

?

IVD, teratoma formation – incorporate into pre-imp. Embryos but negative impact on development.

[162]

EPL

+/− 1000 U/ml LIF

50% MEDII conditioned medium/ 50% DMEM/ 10% serum

 

Pluri markers. Reduced naïve and increased primed markers (rel. to ESCs).

?

Not functionally pluripotent

 
  1. X status refers to the activation status of the X chromosome, ✗ = inactive X chromosome, = active X chromosome. DR downregulated, UR upregulated, Epi epiblast, PrE primitive endoderm, IVD in vitro differentiation, pre-imp. pre-implantation, post-imp. post-implantation, GLT germline transmission, pluri pluripotency genes.  = standard culture condition, * = “ground state” of self-renewal, rel. to = relative to