
pmid: 16399505
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.
Mice, Knockout, Receptors, Notch, Physiology, Stem Cells, Pancreatic Ducts, DEVBIO, Cell Differentiation, Mice, Transgenic, Cell Biology, Mice, Diabetes Mellitus, Type 1, Immunoglobulin J Recombination Signal Sequence-Binding Protein, Animals, Insulin, Molecular Biology, Signal Transduction
Mice, Knockout, Receptors, Notch, Physiology, Stem Cells, Pancreatic Ducts, DEVBIO, Cell Differentiation, Mice, Transgenic, Cell Biology, Mice, Diabetes Mellitus, Type 1, Immunoglobulin J Recombination Signal Sequence-Binding Protein, Animals, Insulin, Molecular Biology, Signal Transduction
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