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WIREs Dev Biol
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The endocrine pancreas: insights into development, differentiation, and diabetes

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Abstract In the developing embryo, appropriate patterning of the endoderm fated to become pancreas requires the spatial and temporal coordination of soluble factors secreted by the surrounding tissues. Once pancreatic progenitor cells are specified in the developing gut tube epithelium, epithelial–mesenchymal interactions, as well as a cascade of transcription factors, subsequently delineate three distinct lineages, including endocrine, exocrine, and ductal cells. Simultaneous morphological changes, including branching, vascularization, and proximal organ development, also influence the process of specification and differentiation. Decades of research using mouse genetics have uncovered many of the key factors involved in pancreatic cell fate decisions. When pancreas development or islet cell functions go awry, due to mutations in genes important for proper organogenesis and development, the result can lead to a common pancreatic affliction, diabetes mellitus. Current treatments for diabetes are adequate but not curative. Therefore, researchers are utilizing the current understanding of normal embryonic pancreas development in vivo, to direct embryonic stem cells toward a pancreatic fate with the goal of transplanting these in vitro generated ‘islets’ into patients. Mimicking development in vitro has proven difficult; however, significant progress has been made and the current differentiation protocols are becoming more efficient. The continued partnership between developmental biologists and stem cell researchers will guarantee that the in vitro generation of insulin‐producing β cells is a possible therapeutic option for the treatment of diabetes. WIREs Dev Biol 2011. doi: 10.1002/wdev.44 For further resources related to this article, please visit the WIREs website.

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Pancreatic endoderm patterning and specification. The portion of the endoderm fated to become dorsal and ventral pancreas is patterned and specified due to the influence of secreted molecules and signaling pathways from adjacent tissues and cells. The influence of fibroblast growth factor (FGF) and bone morphogenetic protein (BMP) signaling from the cardiac mesoderm and septum transversum mesenchyme, respectively, affect the patterning of ventral pancreatic endoderm. Retinoic acid (RA), sonic hedgehog (SHH), FGF, and ACTIVIN signaling from the paraxial mesoderm and notochord allow for patterning of the dorsal pancreatic endoderm. The stage from E9.5 through E12.5 marks the primary transition. During this period, the pancreatic progenitor cells are specified, first wave endocrine cells are present, and epithelial branching morphogenesis begins. The secondary transition occurs after E12.5 and is marked by a major wave of endocrine cell specification and development, as well as further ductal morphogenesis and exocrine lineage differentiation.

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Islet cell specification in the developing pancreas. Multipotent pancreatic progenitor cells (PDX1+/PTF1A+/SOX9+) are present in the ductal epithelium in the developing pancreas. In addition, multipotent CPA+/PTF1A+ cells at the tips in early development are multipotent progenitor cells but later in development are restricted to differentiating into only the exocrine lineage. All hormone‐producing endocrine cell lineages are derived from the endocrine progenitor cells (NEUROG3+), which delaminate from the ductal epithelium. Endocrine progenitors can differentiate into all five hormone‐expressing cell types including insulin‐producing β cells, glucagon‐producing α cells, somatostatin‐producing δ cells, pancreatic polypeptide‐producing PP cells and ghrelin‐producing ε cells. As development proceeds, these differentiated hormone+ cells will coalesce and form the islets of Langerhans. The influence of various TFs determines the specific endocrine cell produced.

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Early ‘first wave’ glucagon‐expressing α cells. Early ‘first wave’ α cells are present in mouse models despite the deletion of factors necessary for pancreas development and endocrine specification. Sagittal sections of E10.5 embryos from a representative wild‐type littermate (a), Pdx1 null (b), Ptf1a null (c), Neurog3 null (d), Nkx2‐2 null (e), and pancreas‐specific deletion of Arx (f), were stained by immunofluorescence for the hormone glucagon (a–f). In all images, glucagon‐expressing cells are present. All images are of the dorsal pancreas. DAPI marks all nuclei. 40×.

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Pancreatic and biliary domains in the wild‐type E10.5 embryo. Adjacent sagittal sections from E10.5 wild‐type embryo, stained by immunofluorescence with antibodies against FOXA (a) and PDX1, SOX17 (b). The domains of the dorsal pancreas (dp), ventral pancreas (vp), biliary domain (bil), and septum transversum mesenchyme (stm) are noted. While all domains express FOXA (a), PDX1+ cells are found only in the pancreatic domains, and are distinct from the SOX17+ cells in the biliary domain (b). DAPI marks all nuclei. 20×.

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Pancreatic specification is unaltered in embryos lacking either pancreatic and duodenal homeobox 1 (Pdx1) or pancreas‐specific transcription factor 1a (Ptf1a). Sagittal sections from E10.5 Pdx1 null (a) and wild‐type littermate (b), as well as Ptf1a null (c) and wild‐type littermate (d) embryos were stained by immunofluorescence with antibodies against the transcription factor (TF) FOXA (demarking endoderm) and the hormone glucagon (identifying the pancreatic domain). In both null embryos, the region fated to become the dorsal pancreas (dp) is present, contains glucagon‐expressing cells, and appears similar in both the null and wild‐type. stm is septum transversum mesenchyme. DAPI marks all nuclei. 20×.

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Birth Defects > Organ Anomalies
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