|
|
|
|
|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
First published online 20 August 2008
doi: 10.1242/dev.017137
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Report |
Department of Internal Medicine, Technical University of Munich, 81675 Munich, Germany.
* Author for correspondence (e-mail: roland.schmid{at}lrz.tum.de)
Accepted 1 August 2008
SUMMARY
Recent studies have shown that Wnt/β-catenin signaling is essential for development of the exocrine pancreas, but the role of β-catenin-dependent target genes such as Myc during pancreatic development is not well known. Here, we show that tissue-specific deletion of Myc causes a slightly accelerated differentiation of pancreatic epithelial cells into endocrine cells and perturbs the proliferation of pancreatic progenitors and acinar precursor cells during early development, resulting in a severe reduction of the epithelial cell mass of pancreatic buds and an extensive acinar hypoplasia. Loss of Myc does not affect the expression of the tissue-specific transcription factor PTF1a, which is required for the differentiation of acinar cells. In contrast to its role for exocrine cell growth, the development of endocrine cell lineages is not significantly disturbed. These data suggest that Myc is required for the expansion of the exocrine pancreas. Our observations are consistent with the findings in β-catenin-deficient pancreas, suggesting that Wnt/β-catenin signaling affects the proliferation of pancreatic epithelial cells and acinar precursors through its target gene Myc.
Key words: Myc, Pancreas, Development, Mouse
