Dataset Information


Altered Phenotype of ?-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel.

ABSTRACT: Diffuse congenital hyperinsulinism in infancy (CHI-D) arises from mutations inactivating the KATP channel; however, the phenotype is difficult to explain from electrophysiology alone. Here we studied wider abnormalities in the ?-cell and other pancreatic lineages. Islets were disorganized in CHI-D compared with controls. PAX4 and ARX expression was decreased. A tendency toward increased NKX2.2 expression was consistent with its detection in two-thirds of CHI-D ?-cell nuclei, similar to the fetal pancreas, and implied immature ?-cell function. CHI-D ?-cells also comprised 10% of cells displaying nucleomegaly. In CHI-D, increased proliferation was most elevated in duct (5- to 11-fold) and acinar (7- to 47-fold) lineages. Increased ?-cell proliferation observed in some cases was offset by an increase in apoptosis; this is in keeping with no difference in INSULIN expression or surface area stained for insulin between CHI-D and control pancreas. However, nuclear localization of CDK6 and P27 was markedly enhanced in CHI-D ?-cells compared with cytoplasmic localization in control cells. These combined data support normal ?-cell mass in CHI-D, but with G1/S molecules positioned in favor of cell cycle progression. New molecular abnormalities in ?-cells and marked proliferative increases in other pancreatic lineages indicate CHI-D is not solely a ?-cell disorder.

SUBMITTER: Salisbury RJ 

PROVIDER: S-EPMC4542438 | BioStudies | 2015-01-01T00:00:00Z

REPOSITORIES: biostudies

Similar Datasets

2004-01-01 | S-EPMC365721 | BioStudies
2013-01-01 | S-EPMC3734289 | BioStudies
1000-01-01 | S-EPMC2637887 | BioStudies
2015-01-01 | S-EPMC4669132 | BioStudies
2011-01-01 | S-EPMC3192309 | BioStudies
2020-01-01 | S-EPMC6966704 | BioStudies
2009-01-01 | S-EPMC2799404 | BioStudies
2015-01-01 | S-EPMC4555716 | BioStudies
2011-01-01 | S-EPMC3217340 | BioStudies
2013-01-01 | S-EPMC3902634 | BioStudies