A detailed understanding of the molecular process involved in the proliferation of pancreatic precursor cells would provide key elements for developing new therapeutic strategies to cure type 1 diabetes. In the present study we investigated the potential involvement of hedgehog signaling in proliferating human pancreatic islet-derived mesenchymal (hPIDM) cells, a population of cells that can be successfully expanded and induced to differentiate into an insulin-secreting phenotype. Here we report that in these precursor cells a hedgehog signaling pathway is activated, as shown by Gli1 expression, and that a dose-dependent inhibition of such a pathway by cyclopamine results in a significant reduction of cell proliferation.
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|Titolo:||Hedgehog signaling during expansion of human pancreatic islet-derived precursors.|
|Rivista:||ANNALS OF THE NEW YORK ACADEMY OF SCIENCES|
|Citazione:||Gallo, R., Grieco, F.A., Marselli, L., Ferretti, E., Gulino, A., Marchetti, P., et al. (2008). Hedgehog signaling during expansion of human pancreatic islet-derived precursors. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1150, 43-45.|
|Appare nelle tipologie:||1.1 Articolo in rivista|