Expression data from SOX9 overexpressing EndoC-ßH1 cells. Expression data from SOX9 overexpressing EndoC-ßH1 cells

Human ß cell dedifferentiation as a potent mechanism of diabetes is gaining prominence. Several data suggest an upregulation of the transcription factor SOX9, a progenitor and duct cell marker during ß cell dedifferentiation. However, its targets in such cells need more understanding. Here, we overexpressed SOX9 and a constitutively active mutant (VP16-SOX9∆TAD) in Human pancreatic beta EndoC-ßH1 cells in order to understand its targets. Overall design: EndoC-ßH1 cells were transfected with either MCS-ires-GFP, VP16-ires-GFP, SOX9WT-ires-GFP or VP16-SOX9∆TAD-ires-GFP and FAC sorted 48h post transfection for RNA extraction and hybridization on Affymetrix microarrays