Cellular and molecular mechanisms coordinating pancreas development

Author:

Bastidas-Ponce Aimée1234,Scheibner Katharina1234,Lickert Heiko1234ORCID,Bakhti Mostafa123ORCID

Affiliation:

1. Institute of Diabetes and Regeneration Research, Helmholtz Zentrum München, D-85764 Neuherberg, Germany

2. Institute of Stem Cell Research, Helmholtz Zentrum München, D-85764 Neuherberg, Germany

3. German Center for Diabetes Research (DZD), D-85764 Neuherberg, Germany

4. Technical University of Munich, Medical Faculty, 81675 Munich, Germany

Abstract

ABSTRACT The pancreas is an endoderm-derived glandular organ that participates in the regulation of systemic glucose metabolism and food digestion through the function of its endocrine and exocrine compartments, respectively. While intensive research has explored the signaling pathways and transcriptional programs that govern pancreas development, much remains to be discovered regarding the cellular processes that orchestrate pancreas morphogenesis. Here, we discuss the developmental mechanisms and principles that are known to underlie pancreas development, from induction and lineage formation to morphogenesis and organogenesis. Elucidating such principles will help to identify novel candidate disease genes and unravel the pathogenesis of pancreas-related diseases, such as diabetes, pancreatitis and cancer.

Funder

Helmholtz-Gemeinschaft

Deutsche Forschungsgemeinschaft

Deutsches Zentrum für Diabetes Forschung

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

Reference236 articles.

1. Notch signaling in the pancreas: patterning and cell fate specification;Afelik;Wiley Interdiscip. Rev. Dev. Biol.,2013

2. Notch-mediated patterning and cell fate allocation of pancreatic progenitor cells;Afelik;Development,2012

3. Wnt7b is required for epithelial progenitor growth and operates during epithelial-to-mesenchymal signaling in pancreatic development;Afelik;Dev. Biol.,2015

4. The morphogenesis of the pancreatic mesenchyme is uncoupled from that of the pancreatic epithelium in IPF1/PDX1-deficient mice;Ahlgren;Development,1996

5. β-Cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the β-cell phenotype and maturity onset diabetes;Ahlgren;Genes Dev.,1998

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