Repression of COUP-TFI Improves Bone Marrow-Derived Mesenchymal Stem Cell Differentiation into Insulin-Producing Cells

Repression of COUP-TFI Improves Bone Marrow-Derived Mesenchymal Stem Cell Differentiation into Insulin-Producing Cells

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Identifying molecular mechanisms that regulate insulin expression in bone marrow-derived mesenchymal stem cells (bmMSCs) can provide clues on how to stimulate the differentiation of bmMSCs into insulin-producing cells (IPCs), which can be used as a therapeutic approach against type 1 diabetes (T1D).As repression factors may inhibit differentiation, the efficiency of this process is insufficient for cell transplantation.In this study, we used the mouse insulin 2 (Ins2) promoter sequence and performed a DNA affinity precipitation assay combined with liquid chromatography-mass spectrometry to identify the transcription factor, chicken ovalbumin upstream promoter transcriptional factor I (COUP-TFI).Functionally, bmMSCs were reprogrammed into IPCs via Leather Bracelet With Name Beads Gift Box COUP-TFI suppression and MafA overexpression.

The differentiated cells expressed higher levels of genes specific for islet endocrine cells, and they released C-peptide and insulin in response to glucose stimulation.Transplantation of IPCs into streptozotocin-induced diabetic mice caused a reduction in hyperglycemia.Mechanistically, COUP-TFI bound to the DR1 (direct repeats with 1 spacer) element in Geranium the Ins2 promoter, thereby negatively regulating promoter activity.Taken together, the data provide a novel mechanism by which COUP-TFI acts as a negative regulator in the Ins2 promoter.

The differentiation of bmMSCs into IPCs could be improved by knockdown of COUP-TFI, which may provide a novel stem cell-based therapy for T1D.Keywords: siRNAs, differentiation, stem cell transplantation, diabetes, mesenchymal stem cells.