Notch/Rbp-j signaling prevents premature endocrine and ductal cell differentiation in the pancreas

Cell Metab. 2006 Jan;3(1):59-65. doi: 10.1016/j.cmet.2005.12.005.

Abstract

To investigate the precise role of Notch/Rbp-j signaling in the pancreas, we inactivated Rbp-j by crossing Rbp-j floxed mice with Pdx.cre or Rip.cre transgenic mice. The loss of Rbp-j at the initial stage of pancreatic development induced accelerated alpha and PP cell differentiation and a concomitant decrease in the number of Neurogenin3 (Ngn3)-positive cells at E11.5. Then at E15, elongated tubular structures expressing ductal cell markers were evident; however, differentiation of acinar and all types of endocrine cells were reduced. During later embryonic stages, compensatory acinar cell differentiation was observed. The resultant mice exhibited insulin-deficient diabetes with both endocrine and exocrine pancreatic hypoplasia. In contrast, the loss of Rbp-j specifically in beta cells did not affect beta cell number and function. Thus, our analyses indicate that Notch/Rbp-j signaling prevents premature differentiation of pancreatic progenitor cells into endocrine and ductal cells during early development of the pancreas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation* / genetics
  • Diabetes Mellitus, Type 1 / genetics
  • Immunoglobulin J Recombination Signal Sequence-Binding Protein / deficiency
  • Immunoglobulin J Recombination Signal Sequence-Binding Protein / genetics
  • Immunoglobulin J Recombination Signal Sequence-Binding Protein / physiology*
  • Insulin / deficiency
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Pancreatic Ducts / cytology
  • Pancreatic Ducts / embryology*
  • Pancreatic Ducts / metabolism*
  • Pancreatic Ducts / pathology
  • Receptors, Notch / physiology*
  • Signal Transduction* / genetics
  • Stem Cells

Substances

  • Immunoglobulin J Recombination Signal Sequence-Binding Protein
  • Insulin
  • Rbpj protein, mouse
  • Receptors, Notch