Analysis of Pancreatic Endocrine Development in Gdf11-deficient Mice.
From: Department of Developmental Biology, Hagedorn Research Institute, Gentofte, Denmark.
Developmental dynamics : an official publication of the American Association of Anatomists
- Publish Date: Nov 2006
- ISSN: 1058-8388
- Volume: 235
- Issue: 11
- Pages: 3016-25
- Medium: Print
- Language: English
- Citation (JAMA): Dichmann Darwin S, Yassin Hani, Serup Palle, et al. Analysis of Pancreatic Endocrine Development in Gdf11-deficient Mice.. Dev. Dyn. Nov 2006;235:3016-25
Abstract
Here, we examine the role of GDF11 in pancreatic development. Using in situ hybridization and reverse transcriptase-polymerase chain reaction analyses, we show that Gdf11 transcripts are expressed in embryonic pancreas epithelium before the secondary transition but decrease rapidly afterward. To determine the function of GDF11 during pancreas development, we analyzed Gdf11(-/-) mouse embryos. In such embryos, pancreas size is twofold reduced at embryonic day (E) 18 compared with wild-type littermates. Quantification of the different tissue compartments shows a specific hypoplasia of the exocrine compartment, while the endocrine and ductal compartments are unaffected. Notably, NGN3(+) endocrine precursor cells are increased fourfold at E18, although the amount of endocrine cells in the pancreas of these animals is unchanged compared with wild-type littermates. Similarly, the maturation of endocrine cells as well as the ratio between alpha- and beta-cells appears normal.
Mesh Headings (Keywords): Animals, Bone Morphogenetic Proteins, Embryo, Mammalian, Endocrine Glands, Gene Expression, Immunohistochemistry, Islets of Langerhans, Mice, Mice, Knockout, Mutation, Organ Size, Organogenesis, Pancreas, RNA, Messenger, Reverse Transcriptase Polymerase Chain Reaction, Stem Cells
Check for Full Text / PubMed Unique Identifier (PMID): 16964608
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