It is currently believed that pancreatic progenitor or stem cells exist in
the ductal cell population and that these cells have the ability to be grow
n and differentiated into endocrine cells for the treatment of diabetes. In
this study, we have examined this potential in IMPAN (Immortalized Pancrea
tic) cells. These cells are derived from the adult H-2K(b)-tsA58 transgenic
mouse. We observed an increased m-RNA expression of insulin, proendocrine
gene neurogenin 3, and beta -cell transcription factor Pdx1 when the cells
were grown on bovine collagen I gels. The induction profile of these three
genes was similar under the tested conditions. No glucagon or other endocri
ne-specific transcription factors were detectable. Application of GIP, GLP-
1 derivative NN2211, and activin-A/betacellulin to IMPAN cells in normal cu
lture did not lead to endocrine differentiation. In conclusion, it appears
that the ability of IMPAN cells to mature to endocrine cells is limited. (C
) 2001 Academic Press.