N-cadherin is dispensable for pancreas development but required for beta-cell granule turnover

Genesis. 2010 Jun;48(6):374-81. doi: 10.1002/dvg.20628.

Abstract

The cadherin family of cell adhesion molecules mediates adhesive interactions that are required for the formation and maintenance of tissues. Previously, we demonstrated that N-cadherin, which is required for numerous morphogenetic processes, is expressed in the pancreatic epithelium at E9.5, but later becomes restricted to endocrine aggregates in mice. To study the role of N-cadherin during pancreas formation and function we generated a tissue-specific knockout of N-cadherin in the early pancreatic epithelium by inter-crossing N-cadherin-floxed mice with Pdx1Cre mice. Analysis of pancreas-specific ablation of N-cadherin demonstrates that N-cadherin is dispensable for pancreatic development, but required for beta-cell granule turnover. The number of insulin secretory granules is significantly reduced in N-cadherin-deficient beta-cells, and as a consequence insulin secretion is decreased.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadherins / physiology*
  • Cytoplasmic Granules / metabolism*
  • Female
  • Fluorescent Antibody Technique
  • Gene Expression Regulation, Developmental*
  • Homeodomain Proteins / physiology*
  • Immunoblotting
  • Insulin-Secreting Cells / metabolism*
  • Integrases / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Pancreas / growth & development*
  • Pancreas / metabolism
  • Trans-Activators / physiology*

Substances

  • Cadherins
  • Cdh2 protein, mouse
  • Homeodomain Proteins
  • Trans-Activators
  • pancreatic and duodenal homeobox 1 protein
  • Cre recombinase
  • Integrases