Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm

• Published in: Scientific reports Vol. 11; no. 1; p. 8242
• Main Authors: Markouli, C, De Deckersberg, E Couvreu, Dziedzicka, D, Regin, M, Franck, S, Keller, A, Gheldof, A, Geens, M, Sermon, K, Spits, C
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 15.04.2021; Nature Publishing Group UK; Nature Portfolio
• Subjects: Bone morphogenetic protein 4; Cell culture; Cell differentiation; Cell lines; Deregulation; Endoderm; Epigenetics; Genomes; Mesoderm; Sequence analysis; Signal transduction; Stem cells; Wnt protein
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-87547-7

We identified a human embryonic stem cell subline that fails to respond to the differentiation cues needed to obtain endoderm derivatives, differentiating instead into extra-embryonic mesoderm. RNA-sequencing analysis showed that the subline has hyperactivation of the WNT and BMP4 signalling. Modulation of these pathways with small molecules confirmed them as the cause of the differentiation impairment. While activation of WNT and BMP4 in control cells resulted in a loss of endoderm differentiation and induction of extra-embryonic mesoderm markers, inhibition of these pathways in the subline restored its ability to differentiate. Karyotyping and exome sequencing analysis did not identify any changes in the genome that could account for the pathway deregulation. These findings add to the increasing evidence that different responses of stem cell lines to differentiation protocols are based on genetic and epigenetic factors, inherent to the line or acquired during cell culture.