Primary cilia in pancreatic development and disease

Birth Defects Res C Embryo Today. 2014 Jun;102(2):139-58. doi: 10.1002/bdrc.21063. Epub 2014 May 26.

Abstract

Primary cilia and their anchoring basal bodies are important regulators of a growing list of signaling pathways. Consequently, dysfunction in proteins associated with these structures results in perturbation of the development and function of a spectrum of tissue and cell types. Here, we review the role of cilia in mediating the development and function of the pancreas. We focus on ciliary regulation of major pathways involved in pancreatic development, including Shh, Wnt, TGF-β, Notch, and fibroblast growth factor. We also discuss pancreatic phenotypes associated with ciliary dysfunction, including pancreatic cysts and defects in glucose homeostasis, and explore the potential role of cilia in such defects.

Keywords: FGF; Notch; Shh; TGF-beta; Wnt; cilia; ciliopathies; development; glucose homeostasis; pancreas; pancreatic cysts.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Cilia / pathology*
  • Disease Models, Animal
  • Glucose Metabolism Disorders / genetics
  • Glucose Metabolism Disorders / pathology
  • Humans
  • Organogenesis / genetics*
  • Pancreas / cytology
  • Pancreas / metabolism
  • Pancreas / pathology*
  • Pancreatic Cyst / genetics
  • Pancreatic Cyst / pathology
  • Phenotype
  • Signal Transduction