Differential coupling of self-renewal signaling pathways in murine induced pluripotent stem cells

Luca Orlando, Yolanda Sanchez Ripoll, J Foster, Heather Bone, C Giachino, Melanie J Welham

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The ability to reprogram somatic cells to induced pluripotent stem cells (iPSCs), exhibiting properties similar to those of embryonic stem cells (ESCs), has attracted much attention, with many studies focused on improving efficiency of derivation and unraveling the mechanisms of reprogramming. Despite this widespread interest, our knowledge of the molecular signaling pathways that are active in iPSCs and that play a role in controlling their fate have not been studied in detail. To address this shortfall, we have characterized the influence of different signals on the behavior of a model mouse iPSC line. We demonstrate significant responses of this iPSC line to the presence of serum, which leads to profoundly enhanced proliferation and, depending on the medium used, a reduction in the capacity of the iPSCs to self-renew. Surprisingly, this iPSC line was less sensitive to withdrawal of LIF compared to ESCs, exemplified by maintenance of expression of a Nanog-GFP reporter and enhanced self-renewal in the absence of LIF. While inhibition of phosphoinositide-3 kinase (PI3K) signaling decreased iPSC self-renewal, inhibition of Gsk-3 promoted it, even in the absence of LIF. High passages of this iPSC line displayed altered characteristics, including genetic instability and a reduced ability to self-renew. However, this second feature could be restored upon inhibition of Gsk-3. Collectively, our data suggest modulation of Gsk-3 activity plays a key role in the control of iPSC fate. We propose that more careful consideration should be given to characterization of the molecular pathways that control the fate of different iPSC lines, since perturbations from those observed in naïve pluripotent ESCs could render iPSCs and their derivatives susceptible to aberrant and potentially undesirable behaviors.
Original languageEnglish
Article numbere30234
JournalPLoS ONE
Volume7
Issue number1
DOIs
Publication statusPublished - 23 Jan 2012

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Induced Pluripotent Stem Cells
Stem cells
mice
cell lines
embryonic stem cells
Cell Line
Embryonic Stem Cells
Aptitude
induced pluripotent stem cells
Pluripotent Stem Cells
1-Phosphatidylinositol 4-Kinase
phosphatidylinositol 3-kinase
somatic cells
Phosphatidylinositols
animal models
Maintenance

Cite this

Orlando, L., Sanchez Ripoll, Y., Foster, J., Bone, H., Giachino, C., & Welham, M. J. (2012). Differential coupling of self-renewal signaling pathways in murine induced pluripotent stem cells. PLoS ONE, 7(1), [e30234]. https://doi.org/10.1371/journal.pone.0030234

Differential coupling of self-renewal signaling pathways in murine induced pluripotent stem cells. / Orlando, Luca; Sanchez Ripoll, Yolanda; Foster, J; Bone, Heather; Giachino, C; Welham, Melanie J.

In: PLoS ONE, Vol. 7, No. 1, e30234, 23.01.2012.

Research output: Contribution to journalArticle

Orlando, L, Sanchez Ripoll, Y, Foster, J, Bone, H, Giachino, C & Welham, MJ 2012, 'Differential coupling of self-renewal signaling pathways in murine induced pluripotent stem cells', PLoS ONE, vol. 7, no. 1, e30234. https://doi.org/10.1371/journal.pone.0030234
Orlando L, Sanchez Ripoll Y, Foster J, Bone H, Giachino C, Welham MJ. Differential coupling of self-renewal signaling pathways in murine induced pluripotent stem cells. PLoS ONE. 2012 Jan 23;7(1). e30234. https://doi.org/10.1371/journal.pone.0030234
Orlando, Luca ; Sanchez Ripoll, Yolanda ; Foster, J ; Bone, Heather ; Giachino, C ; Welham, Melanie J. / Differential coupling of self-renewal signaling pathways in murine induced pluripotent stem cells. In: PLoS ONE. 2012 ; Vol. 7, No. 1.
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