Abstract
Somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs) using certain factors. The low efficiency of the reprogramming, as well as the heterogeneity of iPSCs, limits the potential application for iPSCs in cell therapy. Here, we show that lithium chloride (LiCl), a known activator of the Wnt signaling pathway, reduces or enhances the efficiency of iPSC generation from mouse embryonic fibroblasts (MEFs) depending on the timing of its addition during the reprogramming. Our results not only demonstrate a method to improve the efficiency of iPSC formation by LiCL, but also indicate its dual role in this process.
Full Text
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call