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Tankyrase inhibition promotes endocrine commitment of hPSC-derived pancreatic progenitors

ABSTRACT: To improve β-like cell differentiation from human pluripotent stem cells (hPSCs), we aimed to substitute a mechanistically elusive compound – nicotinamide (NA), which promotes pancreatic progenitor (PP) commitment, with a pathway-specific compound. By performing a low-throughput chemical screening, we demonstrated that tankyrase inhibitors (TNKSi) can replace NA and efficiently generate PPs. Surprisingly, highly selective TNKSi, such as WIKI4, generate PPs that give rise to islet-like populations with improved β-like cell frequencies and glucose responsiveness compared to NA-derived PPs. Characterization of differentially expressed genes (DEG) between WIKI4 and NA treatment revealed that WIKI4-derived PPs expressed higher levels of genes associated with integrin signalling and actin cytoskeleton pathways. Our findings show that compared to NA, WIKI4 treatment promotes changes in cell shape and motility. Together, our results provide novel insights into pancreatic differentiation and a model that better recapitulates native events associated with pancreas and endocrine commitment.

ORGANISM(S): Homo sapiens

PROVIDER: GSE267833 | GEO | 2024/08/26

REPOSITORIES: GEO

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Identification of response signatures for tankyrase inhibitor treatment in tumor cell lines

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2021-06-18 | GSE162648 | GEO

Tankyrase inhibition promotes endocrine commitment of hPSC-derived pancreatic progenitors

Project description:Tankyrase inhibition promotes endocrine commitment of hPSC-derived pancreatic progenitors

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Identification of response signatures for tankyrase inhibitor treatment in tumor cell lines

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