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Free keywords:
INSULIN-PRODUCING CELLS; EMBRYONIC STEM-CELLS; BETA-CELL; MOUSE
PANCREAS; IN-VITRO; GENE-EXPRESSION; PRECURSOR CELLS; ENDOCRINE-CELLS;
HUMAN ISLETS; DIFFERENTIATIONEndocrinology & Metabolism; Cell hypoxia; Mouse Mafa protein; Mouse Neurog3 protein; Stem cells;
Pancreatic and duodenal homeobox 1 protein;
Abstract:
BACKGROUND: Recent studies suggest that stem cells may represent a putative source for the generation of beta cells. However, the identity and characteristics of stem cells from adult pancreas and conditions for their large scale expansion are still poorly defined.
METHODS: DPC were isolated from adult pancreatic ducts of C57BI/6 mice. Expression profile was investigated by PCR, FAGS and immunohistochemistry.
RESULTS: DPC express a panel of stem cell associated markers such as Pdx-1, cytokeratin-19 (CK19), nestin, Sox9 together with the transcription factor MafA and hepatic nuclear factors HNF1 beta, HNF3 beta, HNF4 alpha and HNF6. This gene expression profile is suggesting that DPC might be a promising tool for endocrine diMrentiation. Atter stimulation with picolinic acid and hypoxia, DPC expressed the endocrine differentiation marker Ngn3. Nevertheless, insulin production was not observed.
CONCLUSIONS: We here describe a protocol for the isolation end expansion of murine pancreatic ductal progenitor cells (DPC) displaying high self-renewal, spheroid-and colony-forming capacity. Further studies are required to elucidate the conditions for differentiation into mature pancreatic endocrine cell lineages.
