Islet transplantation for treatment of diabetes is limited by availability of donor islets and requirements for immunosuppression. Stem cell-derived islets might circumvent these issues. SC-islets effectively control glucose metabolism post transplantation, but do not yet achieve full function with current published differentiation protocols. We aimed to identify markers of mature subpopulations of SC-β cells by studying transcriptional changes associated with maturation of SC-β cells using RNA-seq and co-expression network analysis. The β cell-specific hormone islet amyloid polypeptide (IAPP) emerged as the top candidate to be such a marker. IAPP cells had more mature β cell gene expression and higher cellular insulin content than IAPP cells . IAPP INS cells were more stable in long-term culture than IAPP INS cells and retained insulin expression after transplantation into mice. Finally, we conducted a small molecule screen to identify compounds that enhance IAPP expression. Aconitine up-regulated IAPP and could help to optimize differentiation protocols.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11030367PMC
http://dx.doi.org/10.1101/2024.04.10.587726DOI Listing

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