Excess of O-linked N-acetylglucosamine modifies human pluripotent stem cell differentiation

O-linked-N-acetylglucosamine (O-GlcNAc), a post translational modification, has emerged as an important cue in controlling key cell mechanisms. Here, we investigate O-GlcNAc's role in the maintenance and differentiation of human pluripotent stem cells (hPSC). We reveal that protein expression of O-GlcNAc transferase and hydrolase both decreases during hPSC differentiation. Upregulating O-GlcNAc with O-GlcNAc hydrolase inhibitors has no significant effect on either the maintenance of pluripotency in hPSC culture, or the loss of pluripotency in differentiating hPSC. However, in spontaneously differentiating hPSC, excess O-GlcNAc alters the expression of specific lineage markers: decrease of ectoderm markers (PAX6 by 53–88%, MSX1 by 26–49%) and increase of adipose-related mesoderm markers (PPARγ by 28–100%, C/EBPα by 46–135%). All other lineage markers tested (cardiac, visceral-endoderm, trophectoderm) remain minimally affected by upregulated O-GlcNAc. Interestingly, we also show that excess O-GlcNAc triggers a feedback mechanism that increases O-GlcNAc hydrolase expression by 29–91%. To the best of our knowledge, this is the first report demonstrating that excess O-GlcNAc does not affect hPSC pluripotency in undifferentiated maintenance cultures; instead, it restricts the hPSC differentiation towards specific cell lineages. These data will be useful for developing targeted differentiation protocols and aid in understanding the effects of O-GlcNAc on hPSC differentiation. •O-GlcNAc is not involved in the maintenance or loss of hPSC pluripotency•Excess O-GlcNAc decreases hPSC differentiation towards ectoderm lineage•Excess O-GlcNAc increases hPSC differentiation towards adipose lineage•Excess O-GlcNAc triggers a counter mechanism increasing O-GlcNAc hydrolase level