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

Diabetes. 2015 Sep;64(9):3182-8. doi: 10.2337/db14-1202. Epub 2015 Apr 30.

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 β-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 δ-cell nuclei, similar to the fetal pancreas, and implied immature δ-cell function. CHI-D δ-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 β-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 β-cells compared with cytoplasmic localization in control cells. These combined data support normal β-cell mass in CHI-D, but with G1/S molecules positioned in favor of cell cycle progression. New molecular abnormalities in δ-cells and marked proliferative increases in other pancreatic lineages indicate CHI-D is not solely a β-cell disorder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Cell Lineage
  • Cell Proliferation
  • Child
  • Child, Preschool
  • Congenital Hyperinsulinism / genetics*
  • Congenital Hyperinsulinism / metabolism
  • Cyclin-Dependent Kinase 6 / metabolism
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism
  • Fetus / cytology
  • Glucagon-Secreting Cells / cytology
  • Glucagon-Secreting Cells / metabolism*
  • Homeobox Protein Nkx-2.2
  • Homeodomain Proteins / metabolism
  • Humans
  • Infant
  • Infant, Newborn
  • Insulin / metabolism
  • Insulin-Secreting Cells / cytology
  • Insulin-Secreting Cells / metabolism*
  • Mutation
  • Nuclear Proteins
  • Paired Box Transcription Factors / metabolism
  • Potassium Channels, Inwardly Rectifying / genetics
  • Somatostatin-Secreting Cells / cytology
  • Somatostatin-Secreting Cells / metabolism*
  • Sulfonylurea Receptors / genetics
  • Transcription Factors / metabolism
  • Zebrafish Proteins

Substances

  • ABCC8 protein, human
  • ARX protein, human
  • CDKN1B protein, human
  • Homeobox Protein Nkx-2.2
  • Homeodomain Proteins
  • Insulin
  • Kir6.2 channel
  • NKX2-2 protein, human
  • Nuclear Proteins
  • PAX4 protein, human
  • Paired Box Transcription Factors
  • Potassium Channels, Inwardly Rectifying
  • Sulfonylurea Receptors
  • Transcription Factors
  • Zebrafish Proteins
  • nkx2.2b protein, zebrafish
  • Cyclin-Dependent Kinase Inhibitor p27
  • CDK6 protein, human
  • Cyclin-Dependent Kinase 6