Journal article

Src family kinases and p38 mitogen-activated protein kinases regulate pluripotent cell differentiation in culture

BSN Tan, J Kwek, CKE Wong, NJ Saner, C Yap, F Felquer, MB Morris, DK Gardner, PD Rathjen, J Rathjen

Plos One | PUBLIC LIBRARY SCIENCE | Published : 2016

Abstract

Multiple pluripotent cell populations, which together comprise the pluripotent cell lineage, have been identified. The mechanisms that control the progression between these populations are still poorly understood. The formation of early primitive ectoderm-like (EPL) cells from mouse embryonic stem (mES) cells provides a model to understand how one such transition is regulated. EPL cells form from mES cells in response to L-proline uptake through the transporter Slc38a2. Using inhibitors of cell signaling we have shown that Src family kinases, p38 MAPK, ERK1/2 and GSK3β are required for the transition between mES and EPL cells. ERK1/2, c-Src and GSK3β are likely to be enforcing a receptive, p..

View full abstract

University of Melbourne Researchers

Grants

Funding Acknowledgements

This work was funded by the University of Melbourne, the Australian Stem Cell Centre (funding agreements P019 and P084), Stem Cells Australia, the David Hay Postgraduate Writing Up award and the University of Tasmania. BSNT was supported by an Endeavour International Postgraduate Research Scholarship and a Melbourne International Research Scholarship. CY was supported by an Australian Postgraduate Awards with additional support from the Australian Stem Cell Centre. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.