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. Author manuscript; available in PMC: 2012 Aug 13.
Published in final edited form as: Biochem J. 2011 Aug 15;438(1):11–23. doi: 10.1042/BJ20102152

Table 5. Dedifferentiation of primed pluripotent stem cells to naïve pluripotent stem cells in mouse and human CDK1, cyclin-dependent kinase 1.

Parent cells (primed pluripotency) Inducer of reversal to a naïve state Success rate Reference
Mouse EpiSCs Transfection of Klf4 and addition of LIF and 2i (the ERK
inhibitor PD0325901 and the GSK3 inhibitor CHIR99021)
0.1–1% [147]
Mouse EpiSCs Transfection of Klf2 and addition of LIF and 2i 0.11% [131]
Mouse EpiSCs Transfection of Nanog and addition of LIF and 2i
Transfection of Nanog and addition of LIF and BMP4
1–10%
Not described 2%
[163]
Mouse EpiSCs One of the following five options in the presence of LIF:
 transfection of Klf4
 transfection of Myc
 addition of Kenpaullone (GSK3b and CDK1/cyclin B
 inhibitor)
 addition of Kenpaullone and CHIR99021
 addition of PD184352 (MEK inhibitor) and CHIR99021
[150]
Mouse EpiSCs Transfection of the nuclear receptor Nr5a1 or Nr5a2 gene with
 the addition of LIF and 2i
1% [152]
Mouse EpiSCs 2i and activation of the JAK/STAT3 pathway with a chimaeric
 receptor
0.5–1.5% [148]
Human ESCs LIF, PD0325901 and SB203580 (p38 inhibitor) Not described [164]
Human iPSCs Reversal to the naïve state by LIF and 2i in addition to the
 continued expression of the transgenes OCT4 , SOX2 and
KLF4
Maintenance of the reversed state by LIF, 2i and forskolin
 (activator of adenylate cyclase) without the three
transgenes
Not described [165]
Human ESCs Transient expression of OCT4 plus KLF4, or KLF2 plus
KLF4, followed by addition of LIF, 2i and forskolin.
Not described [165]