| First Author | Kodama S | Year | 2016 |
| Journal | Sci Rep | Volume | 6 |
| Pages | 21211 | PubMed ID | 26887806 |
| Mgi Jnum | J:250031 | Mgi Id | MGI:6099860 |
| Doi | 10.1038/srep21211 | Citation | Kodama S, et al. (2016) Diabetes Caused by Elastase-Cre-Mediated Pdx1 Inactivation in Mice. Sci Rep 6:21211 |
| abstractText | Endocrine and exocrine pancreas tissues are both derived from the posterior foregut endoderm, however, the interdependence of these two cell types during their formation is not well understood. In this study, we generated mutant mice, in which the exocrine tissue is hypoplastic, in order to reveal a possible requirement for exocrine pancreas tissue in endocrine development and/or function. Since previous studies showed an indispensable role for Pdx1 in pancreas organogenesis, we used Elastase-Cre-mediated recombination to inactivate Pdx1 in the pancreatic exocrine lineage during embryonic stages. Along with exocrine defects, including impaired acinar cell maturation, the mutant mice exhibited substantial endocrine defects, including disturbed tip/trunk patterning of the developing ductal structure, a reduced number of Ngn3-expressing endocrine precursors, and ultimately fewer beta cells. Notably, postnatal expansion of the endocrine cell content was extremely poor, and the mutant mice exhibited impaired glucose homeostasis. These findings suggest the existence of an unknown but essential factor(s) in the adjacent exocrine tissue that regulates proper formation of endocrine precursors and the expansion and function of endocrine tissues during embryonic and postnatal stages. |
